Trajković, Vladimir

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  • Trajković, Vladimir (8)
  • Trajkovic, Vladimir (1)

Author's Bibliography

Uticaj glikemije i lipidnog statusa na morfološke karakteristike nukleusa kod pacijenata sa tip 2 dijabetes melitusom

Martinović, Tamara; Ćirić, Darko; Pantić, Igor; Lalić, Katarina; Rasulić, Iva; Despotović, Sanja; Lalić, Ivana; Đuričić, Danica; Vučićević, Ljubica; Misirkić Marjanović, Maja; Trajković, Vladimir; Bumbaširević, Vladimir; Kravić-Stevović, Tamara

(Beograd: Srpsko lekarsko društvo, Sekcija kliničke biohemije, 2019)

TY  - CONF
AU  - Martinović, Tamara
AU  - Ćirić, Darko
AU  - Pantić, Igor
AU  - Lalić, Katarina
AU  - Rasulić, Iva
AU  - Despotović, Sanja
AU  - Lalić, Ivana
AU  - Đuričić, Danica
AU  - Vučićević, Ljubica
AU  - Misirkić Marjanović, Maja
AU  - Trajković, Vladimir
AU  - Bumbaširević, Vladimir
AU  - Kravić-Stevović, Tamara
PY  - 2019
UR  - https://klinbiolabmed.rs/wp-content/uploads/2022/05/Knjiga-sazetka-Kongresa.pdf
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/6662
AB  - Uvod: Osobine tip 2 dijabetes melitusa (T2DM) su insulinska rezistencija, poremećena sekrecija insulina i hiperglikemija. Kao početna terapija T2DM koristi se metformin. Novija istraživanja su pokazala da u T2DM dolazi do morfoloških promena u izgledu nukleusa u vidu nepravilnosti oblika i binukelacije nukleusa.
Cilj: Cilj istraživanja je da se analiziraju ultrastrukturne karakteristike nukleusa limfocita periferne krvi kod pacijenata sa T2DM pomoću kompjuterizovane analize slike, fraktalne i teksturalne analize, kao i utvrđivanje efekta metformina na karakteristike nukleusa.
Metodologija: Mononuklearne ćelije izolovane iz periferne krvi novootkrivenih T2DM bolesnika, bolesnika lečenih metforminom i zdravih ispitanika analizirane su na transmisionom elektronskom mikroskopu (TEM). Primenom ImageJ programa analizirani su oblik i procenat heterohromatina, kao i fraktalna i teksturalna analiza nukleusa limfocita.
Rezultati: Limfociti zdravih osoba su imali okrugle, predominantno heterohromatične nukleuse i malu količinu citoplazme sa retko prisutnim organelama, dok su limfociti T2DM bolesnika imali euhromatične nukleu uz povećanje strukturnih praznina kod T2DM bolesnika. Nivo glukoze našte i HbA1c koreliraju sa fraktalnom dimenzijom i sa parametrima oblika nukleusa. Postoji korelacija između nivoa triglicerida u krvi i fraktalne dimenzije nukleusa.
Zaključak: Nukleusi limfocita bolesnika sa T2DM su nepravilnog oblika i sa većom količinom euhromatina, a promena njihovog izgleda je u vezi sa nivoom glikemije.
PB  - Beograd: Srpsko lekarsko društvo, Sekcija kliničke biohemije
C3  - Knjiga sažetaka: 1. kongres kliničkih biohemičara i specijalista laboratorijske medicine Srbije sa međunarodnim učešćem;  2019 Nov 27-29; Belgrade, Serbia
T1  - Uticaj glikemije i lipidnog statusa na morfološke karakteristike nukleusa kod pacijenata sa tip 2 dijabetes melitusom
SP  - 58
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_6662
ER  - 
@conference{
author = "Martinović, Tamara and Ćirić, Darko and Pantić, Igor and Lalić, Katarina and Rasulić, Iva and Despotović, Sanja and Lalić, Ivana and Đuričić, Danica and Vučićević, Ljubica and Misirkić Marjanović, Maja and Trajković, Vladimir and Bumbaširević, Vladimir and Kravić-Stevović, Tamara",
year = "2019",
abstract = "Uvod: Osobine tip 2 dijabetes melitusa (T2DM) su insulinska rezistencija, poremećena sekrecija insulina i hiperglikemija. Kao početna terapija T2DM koristi se metformin. Novija istraživanja su pokazala da u T2DM dolazi do morfoloških promena u izgledu nukleusa u vidu nepravilnosti oblika i binukelacije nukleusa.
Cilj: Cilj istraživanja je da se analiziraju ultrastrukturne karakteristike nukleusa limfocita periferne krvi kod pacijenata sa T2DM pomoću kompjuterizovane analize slike, fraktalne i teksturalne analize, kao i utvrđivanje efekta metformina na karakteristike nukleusa.
Metodologija: Mononuklearne ćelije izolovane iz periferne krvi novootkrivenih T2DM bolesnika, bolesnika lečenih metforminom i zdravih ispitanika analizirane su na transmisionom elektronskom mikroskopu (TEM). Primenom ImageJ programa analizirani su oblik i procenat heterohromatina, kao i fraktalna i teksturalna analiza nukleusa limfocita.
Rezultati: Limfociti zdravih osoba su imali okrugle, predominantno heterohromatične nukleuse i malu količinu citoplazme sa retko prisutnim organelama, dok su limfociti T2DM bolesnika imali euhromatične nukleu uz povećanje strukturnih praznina kod T2DM bolesnika. Nivo glukoze našte i HbA1c koreliraju sa fraktalnom dimenzijom i sa parametrima oblika nukleusa. Postoji korelacija između nivoa triglicerida u krvi i fraktalne dimenzije nukleusa.
Zaključak: Nukleusi limfocita bolesnika sa T2DM su nepravilnog oblika i sa većom količinom euhromatina, a promena njihovog izgleda je u vezi sa nivoom glikemije.",
publisher = "Beograd: Srpsko lekarsko društvo, Sekcija kliničke biohemije",
journal = "Knjiga sažetaka: 1. kongres kliničkih biohemičara i specijalista laboratorijske medicine Srbije sa međunarodnim učešćem;  2019 Nov 27-29; Belgrade, Serbia",
title = "Uticaj glikemije i lipidnog statusa na morfološke karakteristike nukleusa kod pacijenata sa tip 2 dijabetes melitusom",
pages = "58",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_6662"
}
Martinović, T., Ćirić, D., Pantić, I., Lalić, K., Rasulić, I., Despotović, S., Lalić, I., Đuričić, D., Vučićević, L., Misirkić Marjanović, M., Trajković, V., Bumbaširević, V.,& Kravić-Stevović, T.. (2019). Uticaj glikemije i lipidnog statusa na morfološke karakteristike nukleusa kod pacijenata sa tip 2 dijabetes melitusom. in Knjiga sažetaka: 1. kongres kliničkih biohemičara i specijalista laboratorijske medicine Srbije sa međunarodnim učešćem;  2019 Nov 27-29; Belgrade, Serbia
Beograd: Srpsko lekarsko društvo, Sekcija kliničke biohemije., 58.
https://hdl.handle.net/21.15107/rcub_ibiss_6662
Martinović T, Ćirić D, Pantić I, Lalić K, Rasulić I, Despotović S, Lalić I, Đuričić D, Vučićević L, Misirkić Marjanović M, Trajković V, Bumbaširević V, Kravić-Stevović T. Uticaj glikemije i lipidnog statusa na morfološke karakteristike nukleusa kod pacijenata sa tip 2 dijabetes melitusom. in Knjiga sažetaka: 1. kongres kliničkih biohemičara i specijalista laboratorijske medicine Srbije sa međunarodnim učešćem;  2019 Nov 27-29; Belgrade, Serbia. 2019;:58.
https://hdl.handle.net/21.15107/rcub_ibiss_6662 .
Martinović, Tamara, Ćirić, Darko, Pantić, Igor, Lalić, Katarina, Rasulić, Iva, Despotović, Sanja, Lalić, Ivana, Đuričić, Danica, Vučićević, Ljubica, Misirkić Marjanović, Maja, Trajković, Vladimir, Bumbaširević, Vladimir, Kravić-Stevović, Tamara, "Uticaj glikemije i lipidnog statusa na morfološke karakteristike nukleusa kod pacijenata sa tip 2 dijabetes melitusom" in Knjiga sažetaka: 1. kongres kliničkih biohemičara i specijalista laboratorijske medicine Srbije sa međunarodnim učešćem;  2019 Nov 27-29; Belgrade, Serbia (2019):58,
https://hdl.handle.net/21.15107/rcub_ibiss_6662 .

Combination of menadione and ascorbate induces oxidative stress and mTOR-dependent cytotoxic autophagy

Despotović, Ana; Tovilović-Kovačević, Gordana; Zogović, Nevena; Harhaji-Trajković, Ljubica; Trajković, Vladimir

(Kragujevac: University of Kragujevac, Faculty of Medical Science, 2018)

TY  - CONF
AU  - Despotović, Ana
AU  - Tovilović-Kovačević, Gordana
AU  - Zogović, Nevena
AU  - Harhaji-Trajković, Ljubica
AU  - Trajković, Vladimir
PY  - 2018
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/6365
AB  - The goal of this study was to investigate ascorbate and menadione potential to induce oxidative stress and autophagy in U251 human glioblastoma cells in vitro. To this purpose, U251 cells were treated with single and combined doses of ascorbate and menadione. Cell viability was assessed by crystal violet test.
Changes in mitochondrial membrane potential, superoxide production, apoptosis, and autophagy were determined by flow cytometry using appropriate fluorochromes (JC-1, MitoSox, Annexin-Propidium iodide, and LysoTracker Red, respectively). Activation of the main autophagy repressor mTOR, and its target
S6K, expression of proautophagic protein p62, and conversion of LC3I to LC3II were assessed by immunoblot, while transfection with LC3 siRNA was used to determine the role of autophagy in glioma cell death. Treatment with single doses of ascorbate and menadione did not affect the viability of U251 cells, while their combination resulted in significant dose-dependent cytotoxic effect. This was associated with mitochondrial depolarization followed by increase in concentration of mitochondria-derived superoxide, and finally by apoptosis. Menadione and cotreatment induced increase in the content of acidic autophagic-like vesicles and autophagosome-associated LC3II protein, while decreased concentration of autophagic proteolysis substrate p62. The expression of LC3II was additionally elevated in the presence of proteolysis inhibitor, suggesting increase in autophagic flux. Reduced activity of mTOR and S6K indicate that detected autophagy was mTOR-dependent. Induced autophagy was cytotoxic, since its inhibition by LC3 RNA interference recovered viability of glioma cells. To conclude, combination of ascorbate and menadione synergistically induced oxidative stress, apoptosis, and mTOR-dependent cytotoxic autophagy in U251 cells.
PB  - Kragujevac: University of Kragujevac, Faculty of Medical Science
C3  - Final program and abstract book: 8th International Congress of Pathophysiology, Satelite Symposium: Oxidative Stress in Health and Disease: from Basic Science to Applied Investigations; 2018 Sep 03; Kragujevac, Serbia
T1  - Combination of menadione and ascorbate induces oxidative stress and mTOR-dependent cytotoxic autophagy
SP  - 34
EP  - 34
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_6365
ER  - 
@conference{
author = "Despotović, Ana and Tovilović-Kovačević, Gordana and Zogović, Nevena and Harhaji-Trajković, Ljubica and Trajković, Vladimir",
year = "2018",
abstract = "The goal of this study was to investigate ascorbate and menadione potential to induce oxidative stress and autophagy in U251 human glioblastoma cells in vitro. To this purpose, U251 cells were treated with single and combined doses of ascorbate and menadione. Cell viability was assessed by crystal violet test.
Changes in mitochondrial membrane potential, superoxide production, apoptosis, and autophagy were determined by flow cytometry using appropriate fluorochromes (JC-1, MitoSox, Annexin-Propidium iodide, and LysoTracker Red, respectively). Activation of the main autophagy repressor mTOR, and its target
S6K, expression of proautophagic protein p62, and conversion of LC3I to LC3II were assessed by immunoblot, while transfection with LC3 siRNA was used to determine the role of autophagy in glioma cell death. Treatment with single doses of ascorbate and menadione did not affect the viability of U251 cells, while their combination resulted in significant dose-dependent cytotoxic effect. This was associated with mitochondrial depolarization followed by increase in concentration of mitochondria-derived superoxide, and finally by apoptosis. Menadione and cotreatment induced increase in the content of acidic autophagic-like vesicles and autophagosome-associated LC3II protein, while decreased concentration of autophagic proteolysis substrate p62. The expression of LC3II was additionally elevated in the presence of proteolysis inhibitor, suggesting increase in autophagic flux. Reduced activity of mTOR and S6K indicate that detected autophagy was mTOR-dependent. Induced autophagy was cytotoxic, since its inhibition by LC3 RNA interference recovered viability of glioma cells. To conclude, combination of ascorbate and menadione synergistically induced oxidative stress, apoptosis, and mTOR-dependent cytotoxic autophagy in U251 cells.",
publisher = "Kragujevac: University of Kragujevac, Faculty of Medical Science",
journal = "Final program and abstract book: 8th International Congress of Pathophysiology, Satelite Symposium: Oxidative Stress in Health and Disease: from Basic Science to Applied Investigations; 2018 Sep 03; Kragujevac, Serbia",
title = "Combination of menadione and ascorbate induces oxidative stress and mTOR-dependent cytotoxic autophagy",
pages = "34-34",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_6365"
}
Despotović, A., Tovilović-Kovačević, G., Zogović, N., Harhaji-Trajković, L.,& Trajković, V.. (2018). Combination of menadione and ascorbate induces oxidative stress and mTOR-dependent cytotoxic autophagy. in Final program and abstract book: 8th International Congress of Pathophysiology, Satelite Symposium: Oxidative Stress in Health and Disease: from Basic Science to Applied Investigations; 2018 Sep 03; Kragujevac, Serbia
Kragujevac: University of Kragujevac, Faculty of Medical Science., 34-34.
https://hdl.handle.net/21.15107/rcub_ibiss_6365
Despotović A, Tovilović-Kovačević G, Zogović N, Harhaji-Trajković L, Trajković V. Combination of menadione and ascorbate induces oxidative stress and mTOR-dependent cytotoxic autophagy. in Final program and abstract book: 8th International Congress of Pathophysiology, Satelite Symposium: Oxidative Stress in Health and Disease: from Basic Science to Applied Investigations; 2018 Sep 03; Kragujevac, Serbia. 2018;:34-34.
https://hdl.handle.net/21.15107/rcub_ibiss_6365 .
Despotović, Ana, Tovilović-Kovačević, Gordana, Zogović, Nevena, Harhaji-Trajković, Ljubica, Trajković, Vladimir, "Combination of menadione and ascorbate induces oxidative stress and mTOR-dependent cytotoxic autophagy" in Final program and abstract book: 8th International Congress of Pathophysiology, Satelite Symposium: Oxidative Stress in Health and Disease: from Basic Science to Applied Investigations; 2018 Sep 03; Kragujevac, Serbia (2018):34-34,
https://hdl.handle.net/21.15107/rcub_ibiss_6365 .

Autophagy-independent increase of ATG5 expression in T cells of multiple sclerosis patients.

Paunović, Verica; Vukovič Petrović, Irena; Milenković, Marina; Janjetović, Kristina; Pravica, Vera; Dujmović, Irena; Milošević, Emina; Martinović, Vanja; Mesaroš, Šarlota; Drulović, Jelena; Trajković, Vladimir

(2018)

TY  - JOUR
AU  - Paunović, Verica
AU  - Vukovič Petrović, Irena
AU  - Milenković, Marina
AU  - Janjetović, Kristina
AU  - Pravica, Vera
AU  - Dujmović, Irena
AU  - Milošević, Emina
AU  - Martinović, Vanja
AU  - Mesaroš, Šarlota
AU  - Drulović, Jelena
AU  - Trajković, Vladimir
PY  - 2018
UR  - http://www.jni-journal.com/article/S0165-5728(17)30538-6/abstract
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3014
AB  - Autophagy, a process of controlled self-digestion which regulates cell homeostasis, is involved in innate and adaptive immunity. We investigated the expression of autophagy genes and autophagic activity in distinct lymphocyte populations in treatment-naive MS patients. The mRNA and protein levels of autophagy-related (ATG)5, required for autophagosome formation, were increased in CD4+and CD4-T cells, but not B cells of MS patients compared to control subjects. The expression of other investigated autophagy genes, as well as the autophagic activity, did not significantly differ between the two groups. ATG5 mRNA levels in CD4+T cells from MS patients were positively correlated with those of the proinflammatory cytokine tumor necrosis factor. These data suggest that autophagy-independent increase in ATG5 expression might be associated with the proinflammatory capacity of T cells in multiple sclerosis.
T2  - Journal of Neuroimmunology
T1  - Autophagy-independent increase of ATG5 expression in T cells of multiple sclerosis patients.
VL  - 319
DO  - 10.1016/j.jneuroim.2018.03.001
SP  - 100
EP  - 105
ER  - 
@article{
author = "Paunović, Verica and Vukovič Petrović, Irena and Milenković, Marina and Janjetović, Kristina and Pravica, Vera and Dujmović, Irena and Milošević, Emina and Martinović, Vanja and Mesaroš, Šarlota and Drulović, Jelena and Trajković, Vladimir",
year = "2018",
abstract = "Autophagy, a process of controlled self-digestion which regulates cell homeostasis, is involved in innate and adaptive immunity. We investigated the expression of autophagy genes and autophagic activity in distinct lymphocyte populations in treatment-naive MS patients. The mRNA and protein levels of autophagy-related (ATG)5, required for autophagosome formation, were increased in CD4+and CD4-T cells, but not B cells of MS patients compared to control subjects. The expression of other investigated autophagy genes, as well as the autophagic activity, did not significantly differ between the two groups. ATG5 mRNA levels in CD4+T cells from MS patients were positively correlated with those of the proinflammatory cytokine tumor necrosis factor. These data suggest that autophagy-independent increase in ATG5 expression might be associated with the proinflammatory capacity of T cells in multiple sclerosis.",
journal = "Journal of Neuroimmunology",
title = "Autophagy-independent increase of ATG5 expression in T cells of multiple sclerosis patients.",
volume = "319",
doi = "10.1016/j.jneuroim.2018.03.001",
pages = "100-105"
}
Paunović, V., Vukovič Petrović, I., Milenković, M., Janjetović, K., Pravica, V., Dujmović, I., Milošević, E., Martinović, V., Mesaroš, Š., Drulović, J.,& Trajković, V.. (2018). Autophagy-independent increase of ATG5 expression in T cells of multiple sclerosis patients.. in Journal of Neuroimmunology, 319, 100-105.
https://doi.org/10.1016/j.jneuroim.2018.03.001
Paunović V, Vukovič Petrović I, Milenković M, Janjetović K, Pravica V, Dujmović I, Milošević E, Martinović V, Mesaroš Š, Drulović J, Trajković V. Autophagy-independent increase of ATG5 expression in T cells of multiple sclerosis patients.. in Journal of Neuroimmunology. 2018;319:100-105.
doi:10.1016/j.jneuroim.2018.03.001 .
Paunović, Verica, Vukovič Petrović, Irena, Milenković, Marina, Janjetović, Kristina, Pravica, Vera, Dujmović, Irena, Milošević, Emina, Martinović, Vanja, Mesaroš, Šarlota, Drulović, Jelena, Trajković, Vladimir, "Autophagy-independent increase of ATG5 expression in T cells of multiple sclerosis patients." in Journal of Neuroimmunology, 319 (2018):100-105,
https://doi.org/10.1016/j.jneuroim.2018.03.001 . .
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Coordinated activation of AMP-activated protein kinase, extracellular signal-regulated kinase, and autophagy regulates phorbol myristate acetate-induced differentiation of SH-SY5Y neuroblastoma cells

Zogović, Nevena; Tovilović-Kovačević, Gordana; Misirkić Marjanović, Maja; Vučićević, Ljubica; Janjetović, Kristina; Harhaji-Trajković, Ljubica; Trajkovic, Vladimir

(2015)

TY  - JOUR
AU  - Zogović, Nevena
AU  - Tovilović-Kovačević, Gordana
AU  - Misirkić Marjanović, Maja
AU  - Vučićević, Ljubica
AU  - Janjetović, Kristina
AU  - Harhaji-Trajković, Ljubica
AU  - Trajkovic, Vladimir
PY  - 2015
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/1978
AB  - We explored the interplay between the intracellular energy sensor
   AMP-activated protein kinase (AMPK), extracellular signal-regulated
   kinase (ERK), and autophagy in phorbol myristate acetate (PMA)-induced
   neuronal differentiation of SH-SY5Y human neuroblastoma cells.
   PMA-triggered expression of neuronal markers (dopamine transporter,
   microtubule-associated protein 2, -tubulin) was associated with an
   autophagic response, measured by the conversion of
   microtubule-associated protein light chain 3 (LC3)-I to
   autophagosome-bound LC3-II, increase in autophagic flux, and expression
   of autophagy-related (Atg) proteins Atg7 and beclin-1. This coincided
   with the transient activation of AMPK and sustained activation of ERK.
   Pharmacological inhibition or RNA interference-mediated silencing of
   AMPK suppressed PMA-induced expression of neuronal markers, as well as
   ERK activation and autophagy. A selective pharmacological blockade of
   ERK prevented PMA-induced neuronal differentiation and autophagy
   induction without affecting AMPK phosphorylation. Conversely, the
   inhibition of autophagy downstream of AMPK/ERK, either by
   pharmacological agents or LC3 knockdown, promoted the expression of
   neuronal markers, thus indicating a role of autophagy in the suppression
   of PMA-induced differentiation of SH-SY5Y cells. Therefore, PMA-induced
   neuronal differentiation of SH-SY5Y cells depends on a complex interplay
   between AMPK, ERK, and autophagy, in which the stimulatory effects of
   AMPK/ERK signaling are counteracted by the coinciding autophagic
   response.
T2  - Journal of Neurochemistry
T1  - Coordinated activation of AMP-activated protein kinase, extracellular
 signal-regulated kinase, and autophagy regulates phorbol myristate
 acetate-induced differentiation of SH-SY5Y neuroblastoma cells
IS  - 2
VL  - 133
DO  - 10.1111/jnc.12980
SP  - 223
EP  - 232
ER  - 
@article{
author = "Zogović, Nevena and Tovilović-Kovačević, Gordana and Misirkić Marjanović, Maja and Vučićević, Ljubica and Janjetović, Kristina and Harhaji-Trajković, Ljubica and Trajkovic, Vladimir",
year = "2015",
abstract = "We explored the interplay between the intracellular energy sensor
   AMP-activated protein kinase (AMPK), extracellular signal-regulated
   kinase (ERK), and autophagy in phorbol myristate acetate (PMA)-induced
   neuronal differentiation of SH-SY5Y human neuroblastoma cells.
   PMA-triggered expression of neuronal markers (dopamine transporter,
   microtubule-associated protein 2, -tubulin) was associated with an
   autophagic response, measured by the conversion of
   microtubule-associated protein light chain 3 (LC3)-I to
   autophagosome-bound LC3-II, increase in autophagic flux, and expression
   of autophagy-related (Atg) proteins Atg7 and beclin-1. This coincided
   with the transient activation of AMPK and sustained activation of ERK.
   Pharmacological inhibition or RNA interference-mediated silencing of
   AMPK suppressed PMA-induced expression of neuronal markers, as well as
   ERK activation and autophagy. A selective pharmacological blockade of
   ERK prevented PMA-induced neuronal differentiation and autophagy
   induction without affecting AMPK phosphorylation. Conversely, the
   inhibition of autophagy downstream of AMPK/ERK, either by
   pharmacological agents or LC3 knockdown, promoted the expression of
   neuronal markers, thus indicating a role of autophagy in the suppression
   of PMA-induced differentiation of SH-SY5Y cells. Therefore, PMA-induced
   neuronal differentiation of SH-SY5Y cells depends on a complex interplay
   between AMPK, ERK, and autophagy, in which the stimulatory effects of
   AMPK/ERK signaling are counteracted by the coinciding autophagic
   response.",
journal = "Journal of Neurochemistry",
title = "Coordinated activation of AMP-activated protein kinase, extracellular
 signal-regulated kinase, and autophagy regulates phorbol myristate
 acetate-induced differentiation of SH-SY5Y neuroblastoma cells",
number = "2",
volume = "133",
doi = "10.1111/jnc.12980",
pages = "223-232"
}
Zogović, N., Tovilović-Kovačević, G., Misirkić Marjanović, M., Vučićević, L., Janjetović, K., Harhaji-Trajković, L.,& Trajkovic, V.. (2015). Coordinated activation of AMP-activated protein kinase, extracellular
 signal-regulated kinase, and autophagy regulates phorbol myristate
 acetate-induced differentiation of SH-SY5Y neuroblastoma cells. in Journal of Neurochemistry, 133(2), 223-232.
https://doi.org/10.1111/jnc.12980
Zogović N, Tovilović-Kovačević G, Misirkić Marjanović M, Vučićević L, Janjetović K, Harhaji-Trajković L, Trajkovic V. Coordinated activation of AMP-activated protein kinase, extracellular
 signal-regulated kinase, and autophagy regulates phorbol myristate
 acetate-induced differentiation of SH-SY5Y neuroblastoma cells. in Journal of Neurochemistry. 2015;133(2):223-232.
doi:10.1111/jnc.12980 .
Zogović, Nevena, Tovilović-Kovačević, Gordana, Misirkić Marjanović, Maja, Vučićević, Ljubica, Janjetović, Kristina, Harhaji-Trajković, Ljubica, Trajkovic, Vladimir, "Coordinated activation of AMP-activated protein kinase, extracellular
 signal-regulated kinase, and autophagy regulates phorbol myristate
 acetate-induced differentiation of SH-SY5Y neuroblastoma cells" in Journal of Neurochemistry, 133, no. 2 (2015):223-232,
https://doi.org/10.1111/jnc.12980 . .
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Arylpiperazine-mediated activation of Akt protects SH-SY5Y neuroblastoma cells from 6-hydroxydopamine-induced apoptotic and autophagic death

Tovilović-Kovačević, Gordana; Zogović, Nevena; Šoškić, Vukić; Schrattenholz, Andre; Kostić-Rajačić, Slađana; Misirkić Marjanović, Maja; Janjetović, Kristina; Vučićević, Ljubica; Arsikin, Katarina; Harhaji-Trajković, Ljubica; Trajković, Vladimir

(Elsevier Ltd., 2013)

TY  - JOUR
AU  - Tovilović-Kovačević, Gordana
AU  - Zogović, Nevena
AU  - Šoškić, Vukić
AU  - Schrattenholz, Andre
AU  - Kostić-Rajačić, Slađana
AU  - Misirkić Marjanović, Maja
AU  - Janjetović, Kristina
AU  - Vučićević, Ljubica
AU  - Arsikin, Katarina
AU  - Harhaji-Trajković, Ljubica
AU  - Trajković, Vladimir
PY  - 2013
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/6343
AB  - We investigated the ability of 19 recently synthesized arylpiperazine compounds to protect human SHSY5Y neuroblastoma cells from the neurotoxin 6-hydroxydopamine (6-OHDA). The compound with the most potent neuroprotective action was N-{3-[2-(4-phenyl-piperazin-1-yl)-ethyl]-phenyl}-picolinamide (6b), which reduced 6-OHDA-induced apoptotic death through stabilization of mitochondrial membrane and subsequent prevention of superoxide production, caspase activation and DNA fragmentation. 6-OHDA-triggered autophagic response was also reduced by 6b, which prevented inactivation of the main autophagy repressor mTOR, upregulation of proautophagic beclin-1, conversion of microtubule-associated protein 1 light chain 3 (LC3)-I to autophagosome-associated LC3-II, as well as intracytoplasmic acidification induced by 6-OHDA. The inhibition of autophagy using LC3b gene silencing or pharmacological autophagy blockers 3-methyladenine or bafilomycin A1, mimicked the cytoprotective effect of 6b. While the treatment with 6b had no effect on the phosphorylation of proapoptotic MAP kinases ERK and JNK, it markedly increased the phosphorylation of the prosurvival kinase Akt in 6-OHDA-treated cells. Akt inhibitor DEBC or RNA interference-mediated Akt silencing reduced the ability of 6b to block 6-OHDA-triggered apoptotic and autophagic responses, thus confirming their dependency on Akt activation. The cytoprotective effect of 6b was also observed in 6-OHDA-treated neuronal PC12 cells, but not in SH-SY5Y or PC12 cells exposed to 1-methyl-4-phenylpyridinium, indicating that the observed neuroprotection was dependent on the cytotoxic stimulus. Because of the ability to prevent 6-OHDA induced apoptotic/autophagic cell death through activation of Akt, the investigated arylpiperazines could be potential candidates for treatment of neurodegenerative diseases.
PB  - Elsevier Ltd.
T2  - Neuropharmacology
T1  - Arylpiperazine-mediated activation of Akt protects SH-SY5Y neuroblastoma cells from 6-hydroxydopamine-induced apoptotic and autophagic death
VL  - 72
DO  - 10.1016/j.neuropharm.2013.04.037
SP  - 224
EP  - 235
ER  - 
@article{
author = "Tovilović-Kovačević, Gordana and Zogović, Nevena and Šoškić, Vukić and Schrattenholz, Andre and Kostić-Rajačić, Slađana and Misirkić Marjanović, Maja and Janjetović, Kristina and Vučićević, Ljubica and Arsikin, Katarina and Harhaji-Trajković, Ljubica and Trajković, Vladimir",
year = "2013",
abstract = "We investigated the ability of 19 recently synthesized arylpiperazine compounds to protect human SHSY5Y neuroblastoma cells from the neurotoxin 6-hydroxydopamine (6-OHDA). The compound with the most potent neuroprotective action was N-{3-[2-(4-phenyl-piperazin-1-yl)-ethyl]-phenyl}-picolinamide (6b), which reduced 6-OHDA-induced apoptotic death through stabilization of mitochondrial membrane and subsequent prevention of superoxide production, caspase activation and DNA fragmentation. 6-OHDA-triggered autophagic response was also reduced by 6b, which prevented inactivation of the main autophagy repressor mTOR, upregulation of proautophagic beclin-1, conversion of microtubule-associated protein 1 light chain 3 (LC3)-I to autophagosome-associated LC3-II, as well as intracytoplasmic acidification induced by 6-OHDA. The inhibition of autophagy using LC3b gene silencing or pharmacological autophagy blockers 3-methyladenine or bafilomycin A1, mimicked the cytoprotective effect of 6b. While the treatment with 6b had no effect on the phosphorylation of proapoptotic MAP kinases ERK and JNK, it markedly increased the phosphorylation of the prosurvival kinase Akt in 6-OHDA-treated cells. Akt inhibitor DEBC or RNA interference-mediated Akt silencing reduced the ability of 6b to block 6-OHDA-triggered apoptotic and autophagic responses, thus confirming their dependency on Akt activation. The cytoprotective effect of 6b was also observed in 6-OHDA-treated neuronal PC12 cells, but not in SH-SY5Y or PC12 cells exposed to 1-methyl-4-phenylpyridinium, indicating that the observed neuroprotection was dependent on the cytotoxic stimulus. Because of the ability to prevent 6-OHDA induced apoptotic/autophagic cell death through activation of Akt, the investigated arylpiperazines could be potential candidates for treatment of neurodegenerative diseases.",
publisher = "Elsevier Ltd.",
journal = "Neuropharmacology",
title = "Arylpiperazine-mediated activation of Akt protects SH-SY5Y neuroblastoma cells from 6-hydroxydopamine-induced apoptotic and autophagic death",
volume = "72",
doi = "10.1016/j.neuropharm.2013.04.037",
pages = "224-235"
}
Tovilović-Kovačević, G., Zogović, N., Šoškić, V., Schrattenholz, A., Kostić-Rajačić, S., Misirkić Marjanović, M., Janjetović, K., Vučićević, L., Arsikin, K., Harhaji-Trajković, L.,& Trajković, V.. (2013). Arylpiperazine-mediated activation of Akt protects SH-SY5Y neuroblastoma cells from 6-hydroxydopamine-induced apoptotic and autophagic death. in Neuropharmacology
Elsevier Ltd.., 72, 224-235.
https://doi.org/10.1016/j.neuropharm.2013.04.037
Tovilović-Kovačević G, Zogović N, Šoškić V, Schrattenholz A, Kostić-Rajačić S, Misirkić Marjanović M, Janjetović K, Vučićević L, Arsikin K, Harhaji-Trajković L, Trajković V. Arylpiperazine-mediated activation of Akt protects SH-SY5Y neuroblastoma cells from 6-hydroxydopamine-induced apoptotic and autophagic death. in Neuropharmacology. 2013;72:224-235.
doi:10.1016/j.neuropharm.2013.04.037 .
Tovilović-Kovačević, Gordana, Zogović, Nevena, Šoškić, Vukić, Schrattenholz, Andre, Kostić-Rajačić, Slađana, Misirkić Marjanović, Maja, Janjetović, Kristina, Vučićević, Ljubica, Arsikin, Katarina, Harhaji-Trajković, Ljubica, Trajković, Vladimir, "Arylpiperazine-mediated activation of Akt protects SH-SY5Y neuroblastoma cells from 6-hydroxydopamine-induced apoptotic and autophagic death" in Neuropharmacology, 72 (2013):224-235,
https://doi.org/10.1016/j.neuropharm.2013.04.037 . .
17
17
18

AMPK and ERK regulate phorbol myristate acetate induced differentiation of SH-SY5Y neuroblastoma cells trough autophagy-dependent and –independent mehanisms

Kanazir, Selma; Savić, Danijela; Isaković, Aleksandra; Zogović, Nevena; Tovilović-Kovačević, Gordana; Misirkić Marjanović, Maja; Janjetović, Kristina; Vučićević, Ljubica; Trajković, Vladimir

(Belgrade : Serbian Neuroscience Society, 2013)

TY  - CONF
AU  - Zogović, Nevena
AU  - Tovilović-Kovačević, Gordana
AU  - Misirkić Marjanović, Maja
AU  - Janjetović, Kristina
AU  - Vučićević, Ljubica
AU  - Trajković, Vladimir
PY  - 2013
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/6354
AB  - Introduction: Neural differentiation involves
intracellular signaling-controlled maturation of neural
progenitors into cells with fully developed neuronal
phenotype.
Aim: We explored the interplay between the
adenosine monophosphate-activated protein kinase
(AMPK), extracellular signal-regulated kinase (ERK) and
autophagy in phorbol myristate acetate (PMA)-induced
differentiation of SH-SY5Y human neuroblastoma cells.
Methods: The levels of neuronal marker expression
and acidification of autophagic compartments were
determined by flow cytometry of cells labeled with
appropriate antibodies and acridine orange, respectively.
The activation (phosphorylation) of AMPK and ERK, as
well as the levels of autophagic proteins beclin-1, Atg7,
microtubule-associated protein light chain 3 (LC3) and p62,
were assessed using immunoblot. RNA interference was
used for AMPK and LC3 knockdown.
Results: PMA initiated autophagic response in SH-
SY5Y cells simultaneously with activation of AMPK, a
major intracellular energy sensor, and ERK, a kinase
involved in cell proliferation and differentiation.
Pharmacological inhibition of AMPK or AMPK gene
silencing attenuated differentiation of SH-SY5Y cells, as
well as PMA-induced ERK activation and autophagy. A
selective pharmacological blockade of ERK prevented
PMA-induced neuronal differentiation and autophagy
induction, without affecting AMPK phosphorylation. On the
other hand, the inhibition of autophagy downstream of
AMPK/ERK activation, either by pharmacological agents or
LC3 knockdown, actually promoted the expression of
neuronal markers, thus indicating a role for autophagy in
suppression of PMA-induced differentiation of SH-SY5Y
cells.
Conclusion: PMA-induced differentiation of SH-
SY5Y cells depends on a complex interplay between
AMPK, ERK and autophagy, where AMPK and ERK
promote differentiation independently of autophagy, while
simultaneously inhibiting differentiation process through
autophagy-dependent mechanisms.
AB  - Uvod: Diferencijacija neurona je proces
kontrolisan od strane nekoliko unutarćelijskih signala. U
toku diferencijacije dolazi do potpunog sazrevanja
progenitorskih ćelija u neurone.
Cilj: Cilj ovog rada je bio da se ispita uloga protein
kinaze regulisane adenozin monofosfatom (AMPK), kinaze
regulisane vanćelijskim signalima (ERK) i autofagije tokom
diferencijacije humanih neuroblastoma SH-SY5Y izazvane
forbol miristat acetatom (PMA).
Metode: Ekspresija neuronskih markera i
autofagija su praćene pomoću protočnog citofluorimetra
nakon bojenja ćelija sa odgovarajućim antitelima, odnosno
akridin oranžom. Aktivnosti AMPK, ERK, beklina, Atg7,
proteina lakog lanca 3 povezanog sa mikrotubulima (LC3),
p62, p70S6K i aktina su odreñene pomoću imunoblota.
Utišavanje AMPK i LC3 gena je izvedeno pomoću malih
interferirajućih RNK.
Rezultati: Istovremeno sa započinjanjem
autofagije, PMA je aktivirao AMPK protein, glavni
energetski senzor u ćeliji, i ERK kinazu, zaduženu za
regulaciju diferencijacije i proliferacije. Farmakološka
inhibicija AMPK i utišavanje gena za AMPK usporili su
diferencijaciju SH-SY5Y ćelija, i inhibirali su aktivaciju
ERK kinaze i autofagiju izazvane pomoću PMA. Blokiranje
aktivnosti ERK proteina pomoću specifičnog inhibitora
značajno je usporilo diferencijaciju SH-SY5Y ćelija i
autofagiju izazvane posredstvom PMA, bez uticaja na
aktivnost AMPK. Sa druge strane, inhibicija autofagije
nishodno od AMPK/ERK (farmakološka ili utišavanjem
gena za LC3) je povećala ekspresiju neuronskih markera,
što ukazuje na činjenicu da autofagija izazvana pomoću
PMA najverovatnije suprimira diferencijaciju SH-SY5Y
ćelija.
Zaključak: Diferencijaciju SH-SY5Y ćelija
izazvanu posredstvom PMA pospešuju AMPK i ERK
proteini nezavisno od autofagnog procesa. Istovremeno oba
molekula inhibiraju diferencijaciju preko mehanizama
zavisnih od autofagije.
PB  - Belgrade : Serbian Neuroscience Society
C3  - 6th SNS Serbian Neuroscience Society Congress: book of abstracts; 2013 Nov 14-16; Belgrade, Serbia
T1  - AMPK and ERK regulate phorbol myristate acetate induced differentiation of SH-SY5Y neuroblastoma cells trough autophagy-dependent and –independent mehanisms
T1  - Protein kinaza regulisana adenozin monofosfatom i kinaza regulisana vanćelijskim signalima regulišu diferencijaciju SH-SY5Y ćelija neuroblastoma izazvanu forbol miristat acetatom preko mehanizama zavisnih i nezavisnih od autofagije
SP  - 58
EP  - 58
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_6354
ER  - 
@conference{
editor = "Kanazir, Selma, Savić, Danijela, Isaković, Aleksandra",
author = "Zogović, Nevena and Tovilović-Kovačević, Gordana and Misirkić Marjanović, Maja and Janjetović, Kristina and Vučićević, Ljubica and Trajković, Vladimir",
year = "2013",
abstract = "Introduction: Neural differentiation involves
intracellular signaling-controlled maturation of neural
progenitors into cells with fully developed neuronal
phenotype.
Aim: We explored the interplay between the
adenosine monophosphate-activated protein kinase
(AMPK), extracellular signal-regulated kinase (ERK) and
autophagy in phorbol myristate acetate (PMA)-induced
differentiation of SH-SY5Y human neuroblastoma cells.
Methods: The levels of neuronal marker expression
and acidification of autophagic compartments were
determined by flow cytometry of cells labeled with
appropriate antibodies and acridine orange, respectively.
The activation (phosphorylation) of AMPK and ERK, as
well as the levels of autophagic proteins beclin-1, Atg7,
microtubule-associated protein light chain 3 (LC3) and p62,
were assessed using immunoblot. RNA interference was
used for AMPK and LC3 knockdown.
Results: PMA initiated autophagic response in SH-
SY5Y cells simultaneously with activation of AMPK, a
major intracellular energy sensor, and ERK, a kinase
involved in cell proliferation and differentiation.
Pharmacological inhibition of AMPK or AMPK gene
silencing attenuated differentiation of SH-SY5Y cells, as
well as PMA-induced ERK activation and autophagy. A
selective pharmacological blockade of ERK prevented
PMA-induced neuronal differentiation and autophagy
induction, without affecting AMPK phosphorylation. On the
other hand, the inhibition of autophagy downstream of
AMPK/ERK activation, either by pharmacological agents or
LC3 knockdown, actually promoted the expression of
neuronal markers, thus indicating a role for autophagy in
suppression of PMA-induced differentiation of SH-SY5Y
cells.
Conclusion: PMA-induced differentiation of SH-
SY5Y cells depends on a complex interplay between
AMPK, ERK and autophagy, where AMPK and ERK
promote differentiation independently of autophagy, while
simultaneously inhibiting differentiation process through
autophagy-dependent mechanisms., Uvod: Diferencijacija neurona je proces
kontrolisan od strane nekoliko unutarćelijskih signala. U
toku diferencijacije dolazi do potpunog sazrevanja
progenitorskih ćelija u neurone.
Cilj: Cilj ovog rada je bio da se ispita uloga protein
kinaze regulisane adenozin monofosfatom (AMPK), kinaze
regulisane vanćelijskim signalima (ERK) i autofagije tokom
diferencijacije humanih neuroblastoma SH-SY5Y izazvane
forbol miristat acetatom (PMA).
Metode: Ekspresija neuronskih markera i
autofagija su praćene pomoću protočnog citofluorimetra
nakon bojenja ćelija sa odgovarajućim antitelima, odnosno
akridin oranžom. Aktivnosti AMPK, ERK, beklina, Atg7,
proteina lakog lanca 3 povezanog sa mikrotubulima (LC3),
p62, p70S6K i aktina su odreñene pomoću imunoblota.
Utišavanje AMPK i LC3 gena je izvedeno pomoću malih
interferirajućih RNK.
Rezultati: Istovremeno sa započinjanjem
autofagije, PMA je aktivirao AMPK protein, glavni
energetski senzor u ćeliji, i ERK kinazu, zaduženu za
regulaciju diferencijacije i proliferacije. Farmakološka
inhibicija AMPK i utišavanje gena za AMPK usporili su
diferencijaciju SH-SY5Y ćelija, i inhibirali su aktivaciju
ERK kinaze i autofagiju izazvane pomoću PMA. Blokiranje
aktivnosti ERK proteina pomoću specifičnog inhibitora
značajno je usporilo diferencijaciju SH-SY5Y ćelija i
autofagiju izazvane posredstvom PMA, bez uticaja na
aktivnost AMPK. Sa druge strane, inhibicija autofagije
nishodno od AMPK/ERK (farmakološka ili utišavanjem
gena za LC3) je povećala ekspresiju neuronskih markera,
što ukazuje na činjenicu da autofagija izazvana pomoću
PMA najverovatnije suprimira diferencijaciju SH-SY5Y
ćelija.
Zaključak: Diferencijaciju SH-SY5Y ćelija
izazvanu posredstvom PMA pospešuju AMPK i ERK
proteini nezavisno od autofagnog procesa. Istovremeno oba
molekula inhibiraju diferencijaciju preko mehanizama
zavisnih od autofagije.",
publisher = "Belgrade : Serbian Neuroscience Society",
journal = "6th SNS Serbian Neuroscience Society Congress: book of abstracts; 2013 Nov 14-16; Belgrade, Serbia",
title = "AMPK and ERK regulate phorbol myristate acetate induced differentiation of SH-SY5Y neuroblastoma cells trough autophagy-dependent and –independent mehanisms, Protein kinaza regulisana adenozin monofosfatom i kinaza regulisana vanćelijskim signalima regulišu diferencijaciju SH-SY5Y ćelija neuroblastoma izazvanu forbol miristat acetatom preko mehanizama zavisnih i nezavisnih od autofagije",
pages = "58-58",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_6354"
}
Kanazir, S., Savić, D., Isaković, A., Zogović, N., Tovilović-Kovačević, G., Misirkić Marjanović, M., Janjetović, K., Vučićević, L.,& Trajković, V.. (2013). AMPK and ERK regulate phorbol myristate acetate induced differentiation of SH-SY5Y neuroblastoma cells trough autophagy-dependent and –independent mehanisms. in 6th SNS Serbian Neuroscience Society Congress: book of abstracts; 2013 Nov 14-16; Belgrade, Serbia
Belgrade : Serbian Neuroscience Society., 58-58.
https://hdl.handle.net/21.15107/rcub_ibiss_6354
Kanazir S, Savić D, Isaković A, Zogović N, Tovilović-Kovačević G, Misirkić Marjanović M, Janjetović K, Vučićević L, Trajković V. AMPK and ERK regulate phorbol myristate acetate induced differentiation of SH-SY5Y neuroblastoma cells trough autophagy-dependent and –independent mehanisms. in 6th SNS Serbian Neuroscience Society Congress: book of abstracts; 2013 Nov 14-16; Belgrade, Serbia. 2013;:58-58.
https://hdl.handle.net/21.15107/rcub_ibiss_6354 .
Kanazir, Selma, Savić, Danijela, Isaković, Aleksandra, Zogović, Nevena, Tovilović-Kovačević, Gordana, Misirkić Marjanović, Maja, Janjetović, Kristina, Vučićević, Ljubica, Trajković, Vladimir, "AMPK and ERK regulate phorbol myristate acetate induced differentiation of SH-SY5Y neuroblastoma cells trough autophagy-dependent and –independent mehanisms" in 6th SNS Serbian Neuroscience Society Congress: book of abstracts; 2013 Nov 14-16; Belgrade, Serbia (2013):58-58,
https://hdl.handle.net/21.15107/rcub_ibiss_6354 .

Changes in fractal dimension and lacunarity as early markers of UV-induced apoptosis

Pantic, Igor; Harhaji-Trajković, Ljubica; Pantović, Aleksandar; Milošević, Nebojša; Trajković, Vladimir

(Academic Press, 2012)

TY  - JOUR
AU  - Pantic, Igor
AU  - Harhaji-Trajković, Ljubica
AU  - Pantović, Aleksandar
AU  - Milošević, Nebojša
AU  - Trajković, Vladimir
PY  - 2012
UR  - 2-s2.0-84860523993
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/6225
AB  - The aim of our study was to employ fractal analysis for evaluation of ultrastructural changes during early stages of apoptosis. Apoptosis was induced in U251 human glioma cell line by exposure to UVB light. The cells were visualized by optical phase-contrast microscopy and photographed before the UV treatment, immediately after the treatment, as well as at 30 min intervals during 5h observation period. For each of the 32 cells analyzed, cellular and nuclear fractal dimension, as well as nuclear lacunarity, were determined at each time point. Our data demonstrate that cellular ultrastructural complexity determined by fractal dimension and lacunarity significantly decreases after the UV irradiation, with the nuclear lacunarity being a particularly sensitive parameter in detecting early apoptosis. Importantly, fractal analysis was able to detect cellular apoptotic changes earlier than conventional flow cytometric analysis of phosphatidylserine exposure, DNA fragmentation and cell membrane permeabilization. These results indicate that fractal analysis might be a powerful and affordable method for non-invasive early identification of apoptosis in cell cultures.
PB  - Academic Press
T2  - Journal of Theoretical Biology
T1  - Changes in fractal dimension and lacunarity as early markers of UV-induced apoptosis
VL  - 303
DO  - 10.1016/j.jtbi.2012.03.013
SP  - 87
EP  - 92
ER  - 
@article{
author = "Pantic, Igor and Harhaji-Trajković, Ljubica and Pantović, Aleksandar and Milošević, Nebojša and Trajković, Vladimir",
year = "2012",
abstract = "The aim of our study was to employ fractal analysis for evaluation of ultrastructural changes during early stages of apoptosis. Apoptosis was induced in U251 human glioma cell line by exposure to UVB light. The cells were visualized by optical phase-contrast microscopy and photographed before the UV treatment, immediately after the treatment, as well as at 30 min intervals during 5h observation period. For each of the 32 cells analyzed, cellular and nuclear fractal dimension, as well as nuclear lacunarity, were determined at each time point. Our data demonstrate that cellular ultrastructural complexity determined by fractal dimension and lacunarity significantly decreases after the UV irradiation, with the nuclear lacunarity being a particularly sensitive parameter in detecting early apoptosis. Importantly, fractal analysis was able to detect cellular apoptotic changes earlier than conventional flow cytometric analysis of phosphatidylserine exposure, DNA fragmentation and cell membrane permeabilization. These results indicate that fractal analysis might be a powerful and affordable method for non-invasive early identification of apoptosis in cell cultures.",
publisher = "Academic Press",
journal = "Journal of Theoretical Biology",
title = "Changes in fractal dimension and lacunarity as early markers of UV-induced apoptosis",
volume = "303",
doi = "10.1016/j.jtbi.2012.03.013",
pages = "87-92"
}
Pantic, I., Harhaji-Trajković, L., Pantović, A., Milošević, N.,& Trajković, V.. (2012). Changes in fractal dimension and lacunarity as early markers of UV-induced apoptosis. in Journal of Theoretical Biology
Academic Press., 303, 87-92.
https://doi.org/10.1016/j.jtbi.2012.03.013
Pantic I, Harhaji-Trajković L, Pantović A, Milošević N, Trajković V. Changes in fractal dimension and lacunarity as early markers of UV-induced apoptosis. in Journal of Theoretical Biology. 2012;303:87-92.
doi:10.1016/j.jtbi.2012.03.013 .
Pantic, Igor, Harhaji-Trajković, Ljubica, Pantović, Aleksandar, Milošević, Nebojša, Trajković, Vladimir, "Changes in fractal dimension and lacunarity as early markers of UV-induced apoptosis" in Journal of Theoretical Biology, 303 (2012):87-92,
https://doi.org/10.1016/j.jtbi.2012.03.013 . .
38
31
40

Anti-glioma action of aloe emodin: the role of ERK inhibition

Mijatović, Sanja; Maksimović-Ivanić, Danijela; Radović, Julijana; Miljković, Đorđe; Harhaji-Trajković, Ljubica; Vučković, Olivera; Stošić-Grujičić, Stanislava; Mostarica Stojković, Marija; Trajković, Vladimir

(New York: Springer, 2005)

TY  - JOUR
AU  - Mijatović, Sanja
AU  - Maksimović-Ivanić, Danijela
AU  - Radović, Julijana
AU  - Miljković, Đorđe
AU  - Harhaji-Trajković, Ljubica
AU  - Vučković, Olivera
AU  - Stošić-Grujičić, Stanislava
AU  - Mostarica Stojković, Marija
AU  - Trajković, Vladimir
PY  - 2005
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3840
AB  - The effect of aloe emodin (AE), a herbal anthraquinone derivative, on the rat C6 glioma cell line was investigated. In addition to cell cycle block and caspasedependent apoptosis, AE led to the formation of intracytoplasmic acidic vesicles indicative for autophagic cell death. Moreover, differentiation of surviving cells toward the astrocytic lineage was confirmed by typical morphological changes and increased expression of glial fibrillary acidic protein (GFAP). AE did not affect the activation of mitogen-activated protein kinase p38, Jun-N-terminal kinase, or transcription factor NF-kappaB, but markedly inhibited the activation of extracellular signal-regulated kinases 1 and 2 (ERK1/2) in C6 cells. A selective inhibitor of ERK activation, PD98059, mimicked the effects of AE on glioma cell morphology and GFAP expression, but failed to induce either apoptosis or autophagy. Taken together, these results indicate that the anti-glioma action of AE involves ERK-independent induction of both apoptosis and autophagy, as well as ERK inhibition-mediated differentiation of glioma cells.
PB  - New York: Springer
T2  - Cellular and Molecular Life Sciences
T1  - Anti-glioma action of aloe emodin: the role of ERK inhibition
VL  - 62
DO  - 10.1007/s00018-005-4425-8
SP  - 589
EP  - 598
ER  - 
@article{
author = "Mijatović, Sanja and Maksimović-Ivanić, Danijela and Radović, Julijana and Miljković, Đorđe and Harhaji-Trajković, Ljubica and Vučković, Olivera and Stošić-Grujičić, Stanislava and Mostarica Stojković, Marija and Trajković, Vladimir",
year = "2005",
abstract = "The effect of aloe emodin (AE), a herbal anthraquinone derivative, on the rat C6 glioma cell line was investigated. In addition to cell cycle block and caspasedependent apoptosis, AE led to the formation of intracytoplasmic acidic vesicles indicative for autophagic cell death. Moreover, differentiation of surviving cells toward the astrocytic lineage was confirmed by typical morphological changes and increased expression of glial fibrillary acidic protein (GFAP). AE did not affect the activation of mitogen-activated protein kinase p38, Jun-N-terminal kinase, or transcription factor NF-kappaB, but markedly inhibited the activation of extracellular signal-regulated kinases 1 and 2 (ERK1/2) in C6 cells. A selective inhibitor of ERK activation, PD98059, mimicked the effects of AE on glioma cell morphology and GFAP expression, but failed to induce either apoptosis or autophagy. Taken together, these results indicate that the anti-glioma action of AE involves ERK-independent induction of both apoptosis and autophagy, as well as ERK inhibition-mediated differentiation of glioma cells.",
publisher = "New York: Springer",
journal = "Cellular and Molecular Life Sciences",
title = "Anti-glioma action of aloe emodin: the role of ERK inhibition",
volume = "62",
doi = "10.1007/s00018-005-4425-8",
pages = "589-598"
}
Mijatović, S., Maksimović-Ivanić, D., Radović, J., Miljković, Đ., Harhaji-Trajković, L., Vučković, O., Stošić-Grujičić, S., Mostarica Stojković, M.,& Trajković, V.. (2005). Anti-glioma action of aloe emodin: the role of ERK inhibition. in Cellular and Molecular Life Sciences
New York: Springer., 62, 589-598.
https://doi.org/10.1007/s00018-005-4425-8
Mijatović S, Maksimović-Ivanić D, Radović J, Miljković Đ, Harhaji-Trajković L, Vučković O, Stošić-Grujičić S, Mostarica Stojković M, Trajković V. Anti-glioma action of aloe emodin: the role of ERK inhibition. in Cellular and Molecular Life Sciences. 2005;62:589-598.
doi:10.1007/s00018-005-4425-8 .
Mijatović, Sanja, Maksimović-Ivanić, Danijela, Radović, Julijana, Miljković, Đorđe, Harhaji-Trajković, Ljubica, Vučković, Olivera, Stošić-Grujičić, Stanislava, Mostarica Stojković, Marija, Trajković, Vladimir, "Anti-glioma action of aloe emodin: the role of ERK inhibition" in Cellular and Molecular Life Sciences, 62 (2005):589-598,
https://doi.org/10.1007/s00018-005-4425-8 . .
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Aloe-emodin prevents cytokine-induced tumor cell death: the inhibition of auto-toxic nitric oxide release as a potential mechanism

Mijatović, Sanja; Maksimović-Ivanić, Danijela; Radović, Julijana; Popadić, Dusan; Momčilović, Miljana; Harhaji-Trajković, Ljubica; Miljković, Đorđe; Trajković, Vladimir

(New York: Springer, 2004)

TY  - JOUR
AU  - Mijatović, Sanja
AU  - Maksimović-Ivanić, Danijela
AU  - Radović, Julijana
AU  - Popadić, Dusan
AU  - Momčilović, Miljana
AU  - Harhaji-Trajković, Ljubica
AU  - Miljković, Đorđe
AU  - Trajković, Vladimir
PY  - 2004
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3841
AB  - Aloe-emodin (AE) is a plant-derived hydroxyanthraquinone with potential anticancer activity. We investigated the ability of AE to modulate survival of mouse L929 fibrosarcoma and rat C6 astrocytoma cells through interference with the activation of inducible nitric oxide (NO) synthase (NOS) and subsequent production of tumoricidal free radical NO. Somewhat surprisingly, AE in a dose-dependent manner rescued interferon-gamma + interleukin-1-stimulated L929 cells from NO-dependent killing by reducing their autotoxic NO release. The observed protective effect was less pronounced in C6 cells, due to their higher sensitivity to a direct toxic action of the drug. AE-mediated inhibition of tumor cell NO release coincided with a reduction in cytokine-induced accumulation of transcription and translation products of genes encoding inducible NOS and its transcription factor IRF-1, while activation of NF-kappaB remained unaltered. These data indicate that the influence of AE on tumor growth might be more complex that previously recognized, the net effect being determined by the balance between the two opposing actions of the drug: its capacity to directly kill tumor cells, but also to protect them from NO-mediated toxicity.
PB  - New York: Springer
T2  - Cellular and Molecular Life Sciences
T1  - Aloe-emodin prevents cytokine-induced tumor cell death: the inhibition of auto-toxic nitric oxide release as a potential mechanism
IS  - 14
VL  - 61
DO  - 10.1007/s00018-004-4089-9
SP  - 1805
EP  - 1815
ER  - 
@article{
author = "Mijatović, Sanja and Maksimović-Ivanić, Danijela and Radović, Julijana and Popadić, Dusan and Momčilović, Miljana and Harhaji-Trajković, Ljubica and Miljković, Đorđe and Trajković, Vladimir",
year = "2004",
abstract = "Aloe-emodin (AE) is a plant-derived hydroxyanthraquinone with potential anticancer activity. We investigated the ability of AE to modulate survival of mouse L929 fibrosarcoma and rat C6 astrocytoma cells through interference with the activation of inducible nitric oxide (NO) synthase (NOS) and subsequent production of tumoricidal free radical NO. Somewhat surprisingly, AE in a dose-dependent manner rescued interferon-gamma + interleukin-1-stimulated L929 cells from NO-dependent killing by reducing their autotoxic NO release. The observed protective effect was less pronounced in C6 cells, due to their higher sensitivity to a direct toxic action of the drug. AE-mediated inhibition of tumor cell NO release coincided with a reduction in cytokine-induced accumulation of transcription and translation products of genes encoding inducible NOS and its transcription factor IRF-1, while activation of NF-kappaB remained unaltered. These data indicate that the influence of AE on tumor growth might be more complex that previously recognized, the net effect being determined by the balance between the two opposing actions of the drug: its capacity to directly kill tumor cells, but also to protect them from NO-mediated toxicity.",
publisher = "New York: Springer",
journal = "Cellular and Molecular Life Sciences",
title = "Aloe-emodin prevents cytokine-induced tumor cell death: the inhibition of auto-toxic nitric oxide release as a potential mechanism",
number = "14",
volume = "61",
doi = "10.1007/s00018-004-4089-9",
pages = "1805-1815"
}
Mijatović, S., Maksimović-Ivanić, D., Radović, J., Popadić, D., Momčilović, M., Harhaji-Trajković, L., Miljković, Đ.,& Trajković, V.. (2004). Aloe-emodin prevents cytokine-induced tumor cell death: the inhibition of auto-toxic nitric oxide release as a potential mechanism. in Cellular and Molecular Life Sciences
New York: Springer., 61(14), 1805-1815.
https://doi.org/10.1007/s00018-004-4089-9
Mijatović S, Maksimović-Ivanić D, Radović J, Popadić D, Momčilović M, Harhaji-Trajković L, Miljković Đ, Trajković V. Aloe-emodin prevents cytokine-induced tumor cell death: the inhibition of auto-toxic nitric oxide release as a potential mechanism. in Cellular and Molecular Life Sciences. 2004;61(14):1805-1815.
doi:10.1007/s00018-004-4089-9 .
Mijatović, Sanja, Maksimović-Ivanić, Danijela, Radović, Julijana, Popadić, Dusan, Momčilović, Miljana, Harhaji-Trajković, Ljubica, Miljković, Đorđe, Trajković, Vladimir, "Aloe-emodin prevents cytokine-induced tumor cell death: the inhibition of auto-toxic nitric oxide release as a potential mechanism" in Cellular and Molecular Life Sciences, 61, no. 14 (2004):1805-1815,
https://doi.org/10.1007/s00018-004-4089-9 . .
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