Milošević, Milena

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  • Milošević, Milena (4)
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Elektrofiziološka karakterizacija β ćelija pankreasa na ćelijskoj liniji RIN – 5f

Bošnjaković, Tamara; Todorović, Nataša; Milošević, Milena; Živić, Miroslav

(Belgrade: Serbian Biological Society, 2022)

TY  - CONF
AU  - Bošnjaković, Tamara
AU  - Todorović, Nataša
AU  - Milošević, Milena
AU  - Živić, Miroslav
PY  - 2022
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5743
AB  - Prihvaćeni model lučenja insulina, po stimulaciji glukozom β ćelija pankreasa, čine: (1) transport glukoze u ćeliju; (2) KATP kanali čija blokada ATP-om dovodi do depolarizacije membrane; (3) voltažno-zavisni kalcijumski kanali koji se aktiviraju depolarizacijom, dozvoljavajući ulazak Ca2+; (4) egzocitoza insulinskih granula pokrenuta Ca2+ jonima.1 Pošto za dostizanje praga aktivacije nije dovoljno samo zatvaranje KATP kanala, jasno je da je uključena i aktivnost drugih jonskih kanala. Ima podataka da je ovaj proces posredovan kanalom VRAC (Volume-Regulated Anion Channel) koji provodi jone hlora i osmolite i aktivira se u hipotoničnoj sredini.2 Mi smo koristili metodu nametnute voltaže na deliću membrane uz oslikavanje signala Ca2+ indikatora, kako bi ispitali prisustvo i ulogu VRAC u električnoj aktivnosti RIN – 5f ćelija, u cilju utvrđivanja potencijalnih ograničenja i optimizacije eksperimentalnog pristupa izučavanja strujnog odgovora β ćelija. U prisustvu cezijuma (Cs+ pip), kojim se blokiraju K kanali, snimljene su familije struja u izotoničnim i hipotoničnim uslovima, kao i spontana i depolarizacijom indukovana aktivnost (akcioni potencijali i depolarizacija u odgovoru na stimulaciju glukozom). Testiran je efekat jedinog postojećeg farmakološkog alata za blokadu VRAC, DCPIB na membranske struje i na Ca2+ odgovor ćelija. Rezultati ukazuju da: (1) u RIN – 5f ćelijama nema inaktivirajućeg oblika VRAC i da hipotonični uslovi, u odsustvu glukoze, ne dovode do aktivacije struja; (2) u izotoničnim uslovima, DCPIB pored očekivanog delimičnog bloka struja ima i stimulativni efekat na druge izlazne struje; (3) preliminarna oslikavanja Ca2+ signala ukazuju da DCPIB inhibira a njegovo uklanjanje povećava aktivnost u prisustvu 0-15 mM glukoze.
AB  - Прихваћени модел лучења инсулина, по стимулацији глукозом β ћелија панкреаса,
чине: (1) транспорт глукозе у ћелију; (2) KATP канали чија блокада ATP-ом доводи
до деполаризације мембране; (3) волтажно-зависни калцијумски канали који се
активирају деполаризацијом, дозвољавајући улазак Ca2+; (4) егзоцитоза
инсулинских гранула покренута Ca2+ јонима.1 Пошто за достизање прага
активације није довољно само затварање KATP канала, јасно је да је укључена и
активност других јонских канала. Има података да је овај процес посредован
каналом VRAC (Volume-Regulated Anion Channel) који проводи јоне хлора и
осмолите и активира се у хипотоничној средини.2 Ми смо користили методу
наметнуте волтаже на делићу мембране уз осликавање сигнала Ca2+ индикатора,
како би испитали присуство и улогу VRAC у електричној активности RIN – 5f
ћелија, у циљу утврђивања потенцијалних ограничења и оптимизације
експерименталног приступа изучавања струјног одговора β ћелија. У присуству
цезијума (Cs+pip), којим се блокирају K канали, снимљене су фамилије струја у
изотоничним и хипотоничним условима, као и спонтана и деполаризацијом
индукована активност (акциони потенцијали и деполаризација у одговору на
стимулацију глукозом). Тестиран је ефекат јединог постојећег фармаколошког
алата за блокаду VRAC, DCPIB на мембранске струје и на Ca2+ одговор ћелија.
Резултати указују да: (1) у RIN – 5f ћелијама нема инактивирајућег облика VRAC и
да хипотонични услови, у одсуству глукозе, не доводе до активације струја; (2) у
изотоничним условима, DCPIB поред очекиваног делимичног блока струја има и
стимулативни ефекат на друге излазне струје; (3) прелиминарна осликавања Ca2+
сигнала указују да DCPIB инхибира а његово уклањање повећава активност у
присуству 0-15 mM глукозе.
PB  - Belgrade: Serbian Biological Society
C3  - Knjiga sažetaka: Treći Kongres biologa Srbije: Osnovna i primenjena istraživanja: Metodika nastave; 2022 Sep 21-25; Zlatibor, Serbia
T1  - Elektrofiziološka karakterizacija β ćelija pankreasa na ćelijskoj liniji RIN – 5f
T1  - Електрофизиолошка карактеризација β ћелија панкреаса на ћелијској линији RIN – 5f
SP  - 27
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_5743
ER  - 
@conference{
author = "Bošnjaković, Tamara and Todorović, Nataša and Milošević, Milena and Živić, Miroslav",
year = "2022",
abstract = "Prihvaćeni model lučenja insulina, po stimulaciji glukozom β ćelija pankreasa, čine: (1) transport glukoze u ćeliju; (2) KATP kanali čija blokada ATP-om dovodi do depolarizacije membrane; (3) voltažno-zavisni kalcijumski kanali koji se aktiviraju depolarizacijom, dozvoljavajući ulazak Ca2+; (4) egzocitoza insulinskih granula pokrenuta Ca2+ jonima.1 Pošto za dostizanje praga aktivacije nije dovoljno samo zatvaranje KATP kanala, jasno je da je uključena i aktivnost drugih jonskih kanala. Ima podataka da je ovaj proces posredovan kanalom VRAC (Volume-Regulated Anion Channel) koji provodi jone hlora i osmolite i aktivira se u hipotoničnoj sredini.2 Mi smo koristili metodu nametnute voltaže na deliću membrane uz oslikavanje signala Ca2+ indikatora, kako bi ispitali prisustvo i ulogu VRAC u električnoj aktivnosti RIN – 5f ćelija, u cilju utvrđivanja potencijalnih ograničenja i optimizacije eksperimentalnog pristupa izučavanja strujnog odgovora β ćelija. U prisustvu cezijuma (Cs+ pip), kojim se blokiraju K kanali, snimljene su familije struja u izotoničnim i hipotoničnim uslovima, kao i spontana i depolarizacijom indukovana aktivnost (akcioni potencijali i depolarizacija u odgovoru na stimulaciju glukozom). Testiran je efekat jedinog postojećeg farmakološkog alata za blokadu VRAC, DCPIB na membranske struje i na Ca2+ odgovor ćelija. Rezultati ukazuju da: (1) u RIN – 5f ćelijama nema inaktivirajućeg oblika VRAC i da hipotonični uslovi, u odsustvu glukoze, ne dovode do aktivacije struja; (2) u izotoničnim uslovima, DCPIB pored očekivanog delimičnog bloka struja ima i stimulativni efekat na druge izlazne struje; (3) preliminarna oslikavanja Ca2+ signala ukazuju da DCPIB inhibira a njegovo uklanjanje povećava aktivnost u prisustvu 0-15 mM glukoze., Прихваћени модел лучења инсулина, по стимулацији глукозом β ћелија панкреаса,
чине: (1) транспорт глукозе у ћелију; (2) KATP канали чија блокада ATP-ом доводи
до деполаризације мембране; (3) волтажно-зависни калцијумски канали који се
активирају деполаризацијом, дозвољавајући улазак Ca2+; (4) егзоцитоза
инсулинских гранула покренута Ca2+ јонима.1 Пошто за достизање прага
активације није довољно само затварање KATP канала, јасно је да је укључена и
активност других јонских канала. Има података да је овај процес посредован
каналом VRAC (Volume-Regulated Anion Channel) који проводи јоне хлора и
осмолите и активира се у хипотоничној средини.2 Ми смо користили методу
наметнуте волтаже на делићу мембране уз осликавање сигнала Ca2+ индикатора,
како би испитали присуство и улогу VRAC у електричној активности RIN – 5f
ћелија, у циљу утврђивања потенцијалних ограничења и оптимизације
експерименталног приступа изучавања струјног одговора β ћелија. У присуству
цезијума (Cs+pip), којим се блокирају K канали, снимљене су фамилије струја у
изотоничним и хипотоничним условима, као и спонтана и деполаризацијом
индукована активност (акциони потенцијали и деполаризација у одговору на
стимулацију глукозом). Тестиран је ефекат јединог постојећег фармаколошког
алата за блокаду VRAC, DCPIB на мембранске струје и на Ca2+ одговор ћелија.
Резултати указују да: (1) у RIN – 5f ћелијама нема инактивирајућег облика VRAC и
да хипотонични услови, у одсуству глукозе, не доводе до активације струја; (2) у
изотоничним условима, DCPIB поред очекиваног делимичног блока струја има и
стимулативни ефекат на друге излазне струје; (3) прелиминарна осликавања Ca2+
сигнала указују да DCPIB инхибира а његово уклањање повећава активност у
присуству 0-15 mM глукозе.",
publisher = "Belgrade: Serbian Biological Society",
journal = "Knjiga sažetaka: Treći Kongres biologa Srbije: Osnovna i primenjena istraživanja: Metodika nastave; 2022 Sep 21-25; Zlatibor, Serbia",
title = "Elektrofiziološka karakterizacija β ćelija pankreasa na ćelijskoj liniji RIN – 5f, Електрофизиолошка карактеризација β ћелија панкреаса на ћелијској линији RIN – 5f",
pages = "27",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_5743"
}
Bošnjaković, T., Todorović, N., Milošević, M.,& Živić, M.. (2022). Elektrofiziološka karakterizacija β ćelija pankreasa na ćelijskoj liniji RIN – 5f. in Knjiga sažetaka: Treći Kongres biologa Srbije: Osnovna i primenjena istraživanja: Metodika nastave; 2022 Sep 21-25; Zlatibor, Serbia
Belgrade: Serbian Biological Society., 27.
https://hdl.handle.net/21.15107/rcub_ibiss_5743
Bošnjaković T, Todorović N, Milošević M, Živić M. Elektrofiziološka karakterizacija β ćelija pankreasa na ćelijskoj liniji RIN – 5f. in Knjiga sažetaka: Treći Kongres biologa Srbije: Osnovna i primenjena istraživanja: Metodika nastave; 2022 Sep 21-25; Zlatibor, Serbia. 2022;:27.
https://hdl.handle.net/21.15107/rcub_ibiss_5743 .
Bošnjaković, Tamara, Todorović, Nataša, Milošević, Milena, Živić, Miroslav, "Elektrofiziološka karakterizacija β ćelija pankreasa na ćelijskoj liniji RIN – 5f" in Knjiga sažetaka: Treći Kongres biologa Srbije: Osnovna i primenjena istraživanja: Metodika nastave; 2022 Sep 21-25; Zlatibor, Serbia (2022):27,
https://hdl.handle.net/21.15107/rcub_ibiss_5743 .

Serum IGG fraction from ALS patients alters redox homeostasis in the BV-2 microglial cell line

Milićević, Katarina; Milošević, Milena; Božić, Iva; Lavrnja, Irena; Stevanović, Ivana; Bijelić, Dunja D.; Živković, Irena; Stević, Zorica; Anđus, Pavle R.

(Belgrade: Serbian Neuroscience Society, 2017)

TY  - CONF
AU  - Milićević, Katarina
AU  - Milošević, Milena
AU  - Božić, Iva
AU  - Lavrnja, Irena
AU  - Stevanović, Ivana
AU  - Bijelić, Dunja D.
AU  - Živković, Irena
AU  - Stević, Zorica
AU  - Anđus, Pavle R.
PY  - 2017
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5990
AB  - Introduction. Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder that affects motor neurons. Having in mind well documented facts that on one hand, ALS brain is under oxidative stress, and on the other that non-cell autonomous mechanisms involving glial cells contribute to the disease progression, we wanted to examine the effect of humoral factors immunoglobulins G from ALS patients (ALS IgG) on oxidative stress and antioxidative system of BV-2 microglial cell line. Methods. BV-2 cells were treated with ALS and control IgG (0.1 mg/ml). TNF-α release, oxidative stress markers and antioxidative enzymes activities were determined using biochemical assays (24 h treatment), while gene expression was determined using RT-qPCR (4 h treatment). ROS, cytosolic peroxide and pH alteration were evaluated with carboxy-H2DCFDA, HyPer and SypHer, respectively. Results. All tested ALS IgG (compared with control IgG) induced oxidative stress (rise in NO and lipid peroxidation), release of TNF-α and higher antioxidative defense (elevation of Mn- and Cu,Zn-superoxide dismutase, catalase, glutathione reductase with a decrease of glutathione peroxidase and glutathione). IgG from 4/11 ALS patients induced slow exponential rise of HyPer intensity and lower increase of SypHer intensity. None of the control IgG induced changes with neither of the indicators. Acute ROS generation was detected in 1/3 of ALS samples with carboxy-H2DCFDA. Conclusion. Our study demonstrates the potential role of inflammatory humoral factors, ALS IgGs, as triggers (via ROS generation) of the activation in microglia, known to occur in later stages of the disease.
PB  - Belgrade: Serbian Neuroscience Society
C3  - Book of Abstract: 7th Congress of Serbian Neuroscience Society with international participation; 2017 Oct 25-27; Belgrade, Serbia
T1  - Serum IGG fraction from ALS patients alters redox homeostasis in the BV-2 microglial cell line
SP  - 72
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_5990
ER  - 
@conference{
author = "Milićević, Katarina and Milošević, Milena and Božić, Iva and Lavrnja, Irena and Stevanović, Ivana and Bijelić, Dunja D. and Živković, Irena and Stević, Zorica and Anđus, Pavle R.",
year = "2017",
abstract = "Introduction. Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder that affects motor neurons. Having in mind well documented facts that on one hand, ALS brain is under oxidative stress, and on the other that non-cell autonomous mechanisms involving glial cells contribute to the disease progression, we wanted to examine the effect of humoral factors immunoglobulins G from ALS patients (ALS IgG) on oxidative stress and antioxidative system of BV-2 microglial cell line. Methods. BV-2 cells were treated with ALS and control IgG (0.1 mg/ml). TNF-α release, oxidative stress markers and antioxidative enzymes activities were determined using biochemical assays (24 h treatment), while gene expression was determined using RT-qPCR (4 h treatment). ROS, cytosolic peroxide and pH alteration were evaluated with carboxy-H2DCFDA, HyPer and SypHer, respectively. Results. All tested ALS IgG (compared with control IgG) induced oxidative stress (rise in NO and lipid peroxidation), release of TNF-α and higher antioxidative defense (elevation of Mn- and Cu,Zn-superoxide dismutase, catalase, glutathione reductase with a decrease of glutathione peroxidase and glutathione). IgG from 4/11 ALS patients induced slow exponential rise of HyPer intensity and lower increase of SypHer intensity. None of the control IgG induced changes with neither of the indicators. Acute ROS generation was detected in 1/3 of ALS samples with carboxy-H2DCFDA. Conclusion. Our study demonstrates the potential role of inflammatory humoral factors, ALS IgGs, as triggers (via ROS generation) of the activation in microglia, known to occur in later stages of the disease.",
publisher = "Belgrade: Serbian Neuroscience Society",
journal = "Book of Abstract: 7th Congress of Serbian Neuroscience Society with international participation; 2017 Oct 25-27; Belgrade, Serbia",
title = "Serum IGG fraction from ALS patients alters redox homeostasis in the BV-2 microglial cell line",
pages = "72",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_5990"
}
Milićević, K., Milošević, M., Božić, I., Lavrnja, I., Stevanović, I., Bijelić, D. D., Živković, I., Stević, Z.,& Anđus, P. R.. (2017). Serum IGG fraction from ALS patients alters redox homeostasis in the BV-2 microglial cell line. in Book of Abstract: 7th Congress of Serbian Neuroscience Society with international participation; 2017 Oct 25-27; Belgrade, Serbia
Belgrade: Serbian Neuroscience Society., 72.
https://hdl.handle.net/21.15107/rcub_ibiss_5990
Milićević K, Milošević M, Božić I, Lavrnja I, Stevanović I, Bijelić DD, Živković I, Stević Z, Anđus PR. Serum IGG fraction from ALS patients alters redox homeostasis in the BV-2 microglial cell line. in Book of Abstract: 7th Congress of Serbian Neuroscience Society with international participation; 2017 Oct 25-27; Belgrade, Serbia. 2017;:72.
https://hdl.handle.net/21.15107/rcub_ibiss_5990 .
Milićević, Katarina, Milošević, Milena, Božić, Iva, Lavrnja, Irena, Stevanović, Ivana, Bijelić, Dunja D., Živković, Irena, Stević, Zorica, Anđus, Pavle R., "Serum IGG fraction from ALS patients alters redox homeostasis in the BV-2 microglial cell line" in Book of Abstract: 7th Congress of Serbian Neuroscience Society with international participation; 2017 Oct 25-27; Belgrade, Serbia (2017):72,
https://hdl.handle.net/21.15107/rcub_ibiss_5990 .

Immunoglobulins G from Sera of Amyotrophic Lateral Sclerosis Patients Induce Oxidative Stress and Upregulation of Antioxidative System in BV-2 Microglial Cell Line

Milošević, Milena; Milićević, Katarina; Božić, Iva; Lavrnja, Irena; Stevanović, Ivana; Bijelić, Dunja; Dubaić, Marija; Živković, Irena; Stević, Zorica; Giniatullin, Rashid; Andjus, Pavle

(2017)

TY  - JOUR
AU  - Milošević, Milena
AU  - Milićević, Katarina
AU  - Božić, Iva
AU  - Lavrnja, Irena
AU  - Stevanović, Ivana
AU  - Bijelić, Dunja
AU  - Dubaić, Marija
AU  - Živković, Irena
AU  - Stević, Zorica
AU  - Giniatullin, Rashid
AU  - Andjus, Pavle
PY  - 2017
UR  - http://journal.frontiersin.org/article/10.3389/fimmu.2017.01619/full
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/2928
AB  - Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder with a very fast progression, no diagnostic tool for the presymptomatic phase, and still no effective treatment of the disease. Although ALS affects motor neurons, the overall pathophysiological condition points out to the non-cell autonomous mechanisms, where astrocytes and microglia play crucial roles in the disease progression. We have already shown that IgG from sera of ALS patients (ALS IgG) induce calcium transients and an increase in the mobility of acidic vesicles in cultured rat astrocytes. Having in mind the role of microglia in neurodegeneration, and a well-documented fact that oxidative stress is one of the many components contributing to the disease, we decided to examine the effect of ALS IgG on activation, oxidative stress and antioxidative system of BV-2 microglia, and to evaluate their acute effect on cytosolic peroxide, pH, and on reactive oxygen species (ROS) generation. All tested ALS IgGs (compared to control IgG) induced oxidative stress (rise in nitric oxide and the index of lipid peroxidation) followed by release of TNF-α and higher antioxidative defense (elevation of Mn- and CuZn-superoxide dismutase, catalase, and glutathione reductase with a decrease of glutathione peroxidase and glutathione) after 24 h treatment. Both ALS IgG and control IgG showed same localization on the membrane of BV-2 cells following 24 h treatment. Cytosolic peroxide and pH alteration were evaluated with fluorescent probes HyPer and SypHer, respectively, having in mind that HyPer also reacts to pH changes. Out of 11 tested IgGs from ALS patients, 4 induced slow exponential rise of HyPer signal, with maximal normalized fluorescence in the range 0.2–0.5, also inducing similar increase of SypHer intensity, but of a lower amplitude. None of the control IgGs induced changes with neither of the indicators. Acute ROS generation was detected in one out of three tested ALS samples with carboxy-H2DCFDA. The observed phenomena demonstrate the potential role of inflammatory humoral factors, IgGs, as potential triggers of the activation in microglia, known to occur in later stages of ALS. Therefore, revealing the ALS IgG signaling cascade in microglial cells could offer a valuable molecular biomarker and/or a potential therapeutic target.
T2  - Frontiers in Immunology
T1  - Immunoglobulins G from Sera of Amyotrophic Lateral Sclerosis Patients Induce Oxidative Stress and Upregulation of Antioxidative System in BV-2 Microglial Cell Line
IS  - NOV
VL  - 8
DO  - 10.3389/fimmu.2017.01619
SP  - 1619
ER  - 
@article{
author = "Milošević, Milena and Milićević, Katarina and Božić, Iva and Lavrnja, Irena and Stevanović, Ivana and Bijelić, Dunja and Dubaić, Marija and Živković, Irena and Stević, Zorica and Giniatullin, Rashid and Andjus, Pavle",
year = "2017",
abstract = "Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder with a very fast progression, no diagnostic tool for the presymptomatic phase, and still no effective treatment of the disease. Although ALS affects motor neurons, the overall pathophysiological condition points out to the non-cell autonomous mechanisms, where astrocytes and microglia play crucial roles in the disease progression. We have already shown that IgG from sera of ALS patients (ALS IgG) induce calcium transients and an increase in the mobility of acidic vesicles in cultured rat astrocytes. Having in mind the role of microglia in neurodegeneration, and a well-documented fact that oxidative stress is one of the many components contributing to the disease, we decided to examine the effect of ALS IgG on activation, oxidative stress and antioxidative system of BV-2 microglia, and to evaluate their acute effect on cytosolic peroxide, pH, and on reactive oxygen species (ROS) generation. All tested ALS IgGs (compared to control IgG) induced oxidative stress (rise in nitric oxide and the index of lipid peroxidation) followed by release of TNF-α and higher antioxidative defense (elevation of Mn- and CuZn-superoxide dismutase, catalase, and glutathione reductase with a decrease of glutathione peroxidase and glutathione) after 24 h treatment. Both ALS IgG and control IgG showed same localization on the membrane of BV-2 cells following 24 h treatment. Cytosolic peroxide and pH alteration were evaluated with fluorescent probes HyPer and SypHer, respectively, having in mind that HyPer also reacts to pH changes. Out of 11 tested IgGs from ALS patients, 4 induced slow exponential rise of HyPer signal, with maximal normalized fluorescence in the range 0.2–0.5, also inducing similar increase of SypHer intensity, but of a lower amplitude. None of the control IgGs induced changes with neither of the indicators. Acute ROS generation was detected in one out of three tested ALS samples with carboxy-H2DCFDA. The observed phenomena demonstrate the potential role of inflammatory humoral factors, IgGs, as potential triggers of the activation in microglia, known to occur in later stages of ALS. Therefore, revealing the ALS IgG signaling cascade in microglial cells could offer a valuable molecular biomarker and/or a potential therapeutic target.",
journal = "Frontiers in Immunology",
title = "Immunoglobulins G from Sera of Amyotrophic Lateral Sclerosis Patients Induce Oxidative Stress and Upregulation of Antioxidative System in BV-2 Microglial Cell Line",
number = "NOV",
volume = "8",
doi = "10.3389/fimmu.2017.01619",
pages = "1619"
}
Milošević, M., Milićević, K., Božić, I., Lavrnja, I., Stevanović, I., Bijelić, D., Dubaić, M., Živković, I., Stević, Z., Giniatullin, R.,& Andjus, P.. (2017). Immunoglobulins G from Sera of Amyotrophic Lateral Sclerosis Patients Induce Oxidative Stress and Upregulation of Antioxidative System in BV-2 Microglial Cell Line. in Frontiers in Immunology, 8(NOV), 1619.
https://doi.org/10.3389/fimmu.2017.01619
Milošević M, Milićević K, Božić I, Lavrnja I, Stevanović I, Bijelić D, Dubaić M, Živković I, Stević Z, Giniatullin R, Andjus P. Immunoglobulins G from Sera of Amyotrophic Lateral Sclerosis Patients Induce Oxidative Stress and Upregulation of Antioxidative System in BV-2 Microglial Cell Line. in Frontiers in Immunology. 2017;8(NOV):1619.
doi:10.3389/fimmu.2017.01619 .
Milošević, Milena, Milićević, Katarina, Božić, Iva, Lavrnja, Irena, Stevanović, Ivana, Bijelić, Dunja, Dubaić, Marija, Živković, Irena, Stević, Zorica, Giniatullin, Rashid, Andjus, Pavle, "Immunoglobulins G from Sera of Amyotrophic Lateral Sclerosis Patients Induce Oxidative Stress and Upregulation of Antioxidative System in BV-2 Microglial Cell Line" in Frontiers in Immunology, 8, no. NOV (2017):1619,
https://doi.org/10.3389/fimmu.2017.01619 . .
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Extracellular ATP induces graded reactive response of astrocytes and strengthens their antioxidative defense in vitro

Adžić, Marija; Stevanović, Ivana; Josipović, Nataša; Laketa, Danijela; Lavrnja, Irena; Bjelobaba, Ivana; Božić, Iva; Jovanović, Marija; Milošević, Milena; Nedeljković, Nadežda

(2017)

TY  - JOUR
AU  - Adžić, Marija
AU  - Stevanović, Ivana
AU  - Josipović, Nataša
AU  - Laketa, Danijela
AU  - Lavrnja, Irena
AU  - Bjelobaba, Ivana
AU  - Božić, Iva
AU  - Jovanović, Marija
AU  - Milošević, Milena
AU  - Nedeljković, Nadežda
PY  - 2017
UR  - http://doi.wiley.com/10.1002/jnr.23950
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/2560
AB  - It is widely accepted that adenosine triphosphate (ATP) acts as a universal danger-associated molecular pattern with several known mechanisms for immune cell activation. In the central nervous system, ATP activates microglia and astrocytes and induces a neuroinflammatory response. The aim of the present study was to describe responses of isolated astrocytes to increasing concentrations of ATP (5 µM to 1 mM), which were intended to mimic graded intensity of the extracellular stimulus. The results show that ATP induces graded activation response of astrocytes in terms of the cell proliferation, stellation, shape remodeling, and underlying actin and GFAP filament rearrangement, although the changes occurred without an apparent increase in GFAP and actin protein expression. On the other hand, ATP in the range of applied concentrations did not evoke IL-1β release from cultured astrocytes, nor did it modify the release from LPS and LPS+IFN-γ–primed astrocytes. ATP did not promote astrocyte migration in the wound-healing assay, nor did it increase production of reactive oxygen and nitrogen species and lipid peroxidation. Instead, ATP strengthened the antioxidative defense of astrocytes by inducing Cu/ZnSOD and MnSOD activities and by increasing their glutathione content. Our current results suggest that although ATP triggers several attributes of activated astrocytic phenotype with a magnitude that increases with the concentration, it is not sufficient to induce full-blown reactive phenotype of astrocytes in vitro. © 2016 Wiley Periodicals, Inc.
T2  - Journal of Neuroscience Research
T1  - Extracellular ATP induces graded reactive response of astrocytes and strengthens their antioxidative defense in vitro
IS  - 4
VL  - 95
DO  - 10.1002/jnr.23950
SP  - 1053
EP  - 1066
ER  - 
@article{
author = "Adžić, Marija and Stevanović, Ivana and Josipović, Nataša and Laketa, Danijela and Lavrnja, Irena and Bjelobaba, Ivana and Božić, Iva and Jovanović, Marija and Milošević, Milena and Nedeljković, Nadežda",
year = "2017",
abstract = "It is widely accepted that adenosine triphosphate (ATP) acts as a universal danger-associated molecular pattern with several known mechanisms for immune cell activation. In the central nervous system, ATP activates microglia and astrocytes and induces a neuroinflammatory response. The aim of the present study was to describe responses of isolated astrocytes to increasing concentrations of ATP (5 µM to 1 mM), which were intended to mimic graded intensity of the extracellular stimulus. The results show that ATP induces graded activation response of astrocytes in terms of the cell proliferation, stellation, shape remodeling, and underlying actin and GFAP filament rearrangement, although the changes occurred without an apparent increase in GFAP and actin protein expression. On the other hand, ATP in the range of applied concentrations did not evoke IL-1β release from cultured astrocytes, nor did it modify the release from LPS and LPS+IFN-γ–primed astrocytes. ATP did not promote astrocyte migration in the wound-healing assay, nor did it increase production of reactive oxygen and nitrogen species and lipid peroxidation. Instead, ATP strengthened the antioxidative defense of astrocytes by inducing Cu/ZnSOD and MnSOD activities and by increasing their glutathione content. Our current results suggest that although ATP triggers several attributes of activated astrocytic phenotype with a magnitude that increases with the concentration, it is not sufficient to induce full-blown reactive phenotype of astrocytes in vitro. © 2016 Wiley Periodicals, Inc.",
journal = "Journal of Neuroscience Research",
title = "Extracellular ATP induces graded reactive response of astrocytes and strengthens their antioxidative defense in vitro",
number = "4",
volume = "95",
doi = "10.1002/jnr.23950",
pages = "1053-1066"
}
Adžić, M., Stevanović, I., Josipović, N., Laketa, D., Lavrnja, I., Bjelobaba, I., Božić, I., Jovanović, M., Milošević, M.,& Nedeljković, N.. (2017). Extracellular ATP induces graded reactive response of astrocytes and strengthens their antioxidative defense in vitro. in Journal of Neuroscience Research, 95(4), 1053-1066.
https://doi.org/10.1002/jnr.23950
Adžić M, Stevanović I, Josipović N, Laketa D, Lavrnja I, Bjelobaba I, Božić I, Jovanović M, Milošević M, Nedeljković N. Extracellular ATP induces graded reactive response of astrocytes and strengthens their antioxidative defense in vitro. in Journal of Neuroscience Research. 2017;95(4):1053-1066.
doi:10.1002/jnr.23950 .
Adžić, Marija, Stevanović, Ivana, Josipović, Nataša, Laketa, Danijela, Lavrnja, Irena, Bjelobaba, Ivana, Božić, Iva, Jovanović, Marija, Milošević, Milena, Nedeljković, Nadežda, "Extracellular ATP induces graded reactive response of astrocytes and strengthens their antioxidative defense in vitro" in Journal of Neuroscience Research, 95, no. 4 (2017):1053-1066,
https://doi.org/10.1002/jnr.23950 . .
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