TY  - JOUR
AU  - Jovanovic Krivokuca, M.
AU  - Stefanoska, I.
AU  - Abu Rabi, T.
AU  - Al-Abed, Y.
AU  - Stošić-Grujičić, Stanislava
AU  - Vicovac, Lj
PY  - 2015
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/2009
AB  - Introduction: Macrophage migration inhibitory factor (MIF) is expressed
   by villous and extravillous cytotrophoblast. This study was aimed to
   investigate functional relevance of MIF for human trophoblast.
   Methods: MIF mRNA and protein were documented in cytotrophoblast (CT)
   and extravillous trophoblast cell line HTR-8/SVneo by RT-PCR, Western
   blot (WB), and immunocytochemistry. Recombinant human MIF (rhMIF), or
   its specific inhibitor (S,R)-3-(4-hydroxypheny1)-4,5-dihydro-5-isoxazole
   acetic acid methyl ester (ISO-1) were used in Wound healing migration
   and Matrigel invasion tests. Potential effectors, integrin subunits and
   matrix metalloproteinases (MMP) were studied using WB and gelatin
   zymography, respectively.
   Results: Blocking endogenous MIF by ISO-1 decreased HTR-8/SVneo cell
   migration dose dependently, most significantly with 200 mu g/ml to 65\%
   of control. Supplementation with rhMIF induced a significant stimulation
   to 129\% of control with 200 ng/ml. In CT cell invasion test, ISO-1 at
   200 mu g/ml reduced invasion to 59\% of control, while rhMIF (200 ng/m1)
   induced stimulation to 159\% of control. In HTR-8/SVneo cells, invasion
   was significantly inhibited by ISO-1 to 40\%, and increased to 150\% of
   control by rhMIF (200 ng/ml). Integrin alpha 1 was reduced by ISO-1 in
   both cell types, while integrins alpha 5 and beta 1 were not changed.
   Addition of rhMIF increased integrin alpha 1. In the presence of ISO-1,
   levels of MMP-2 and MMP-9 were reduced in CT and HTR-8/SVneo, while
   rhMIF stimulated MMP-2 in CT and MMP-9 in HTR-8/SVneo cells.
   Conclusion: Reported findings provide the first insight into the
   cellular effects of MIF in human trophoblast, which acts to promote cell
   migration and invasion. (C) 2014 Elsevier Ltd. All rights reserved.
T2  - Placenta
T1  - Pharmacological inhibition of MIF interferes with trophoblast cell
 migration and invasiveness
IS  - 2
VL  - 36
DO  - 10.1016/j.placenta.2014.12.003
SP  - 150
EP  - 159
ER  - 

@article{
author = "Jovanovic Krivokuca, M. and Stefanoska, I. and Abu Rabi, T. and Al-Abed, Y. and Stošić-Grujičić, Stanislava and Vicovac, Lj",
year = "2015",
abstract = "Introduction: Macrophage migration inhibitory factor (MIF) is expressed
   by villous and extravillous cytotrophoblast. This study was aimed to
   investigate functional relevance of MIF for human trophoblast.
   Methods: MIF mRNA and protein were documented in cytotrophoblast (CT)
   and extravillous trophoblast cell line HTR-8/SVneo by RT-PCR, Western
   blot (WB), and immunocytochemistry. Recombinant human MIF (rhMIF), or
   its specific inhibitor (S,R)-3-(4-hydroxypheny1)-4,5-dihydro-5-isoxazole
   acetic acid methyl ester (ISO-1) were used in Wound healing migration
   and Matrigel invasion tests. Potential effectors, integrin subunits and
   matrix metalloproteinases (MMP) were studied using WB and gelatin
   zymography, respectively.
   Results: Blocking endogenous MIF by ISO-1 decreased HTR-8/SVneo cell
   migration dose dependently, most significantly with 200 mu g/ml to 65\%
   of control. Supplementation with rhMIF induced a significant stimulation
   to 129\% of control with 200 ng/ml. In CT cell invasion test, ISO-1 at
   200 mu g/ml reduced invasion to 59\% of control, while rhMIF (200 ng/m1)
   induced stimulation to 159\% of control. In HTR-8/SVneo cells, invasion
   was significantly inhibited by ISO-1 to 40\%, and increased to 150\% of
   control by rhMIF (200 ng/ml). Integrin alpha 1 was reduced by ISO-1 in
   both cell types, while integrins alpha 5 and beta 1 were not changed.
   Addition of rhMIF increased integrin alpha 1. In the presence of ISO-1,
   levels of MMP-2 and MMP-9 were reduced in CT and HTR-8/SVneo, while
   rhMIF stimulated MMP-2 in CT and MMP-9 in HTR-8/SVneo cells.
   Conclusion: Reported findings provide the first insight into the
   cellular effects of MIF in human trophoblast, which acts to promote cell
   migration and invasion. (C) 2014 Elsevier Ltd. All rights reserved.",
journal = "Placenta",
title = "Pharmacological inhibition of MIF interferes with trophoblast cell
 migration and invasiveness",
number = "2",
volume = "36",
doi = "10.1016/j.placenta.2014.12.003",
pages = "150-159"
}

Jovanovic Krivokuca, M., Stefanoska, I., Abu Rabi, T., Al-Abed, Y., Stošić-Grujičić, S.,& Vicovac, L.. (2015). Pharmacological inhibition of MIF interferes with trophoblast cell
 migration and invasiveness. in Placenta, 36(2), 150-159.
https://doi.org/10.1016/j.placenta.2014.12.003

Jovanovic Krivokuca M, Stefanoska I, Abu Rabi T, Al-Abed Y, Stošić-Grujičić S, Vicovac L. Pharmacological inhibition of MIF interferes with trophoblast cell
 migration and invasiveness. in Placenta. 2015;36(2):150-159.
doi:10.1016/j.placenta.2014.12.003 .

Jovanovic Krivokuca, M., Stefanoska, I., Abu Rabi, T., Al-Abed, Y., Stošić-Grujičić, Stanislava, Vicovac, Lj, "Pharmacological inhibition of MIF interferes with trophoblast cell
 migration and invasiveness" in Placenta, 36, no. 2 (2015):150-159,
https://doi.org/10.1016/j.placenta.2014.12.003 . .