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Reports of Biochemistry and Molecular Biology
rbmb.net
Basic Sciences
http://rbmb.net
1
admin
2322-3480
2322-3480
10.61882/rbmb
en
jalali
1401
5
1
gregorian
2022
8
1
11
2
online
1
fulltext
en
Regulation of Focal Adhesion Dynamics and Cell Migration by PLC/PI3K-Mediated Metabolism of PtdIns (4,5) P2 in a Breast Cancer Cell Line
زیست شناسی سلولی
Cell Biology
مقالات اصلی
Original Article
<div style="text-align: justify;"><strong><em>Background: </em></strong>Focal adhesions (FAs) are highly dynamic complex structures that assembled and disassembled on an ongoing basis. The balance between the two processes mediates various aspects of cell behavior, ranging from cell adhesion to cell migration. Assembly and disassembly processes of FAs are<br>
regulated by a variety of cellular signaling proteins and adaptors. We previously demonstrated that local levels of Phosphatidylinositol 4,5‐bisphosphate (PtdIns(4,5)P2) in MDA-MB-231 cells increases during FA assembly and declines during disassembly. In this study we aimed to investigate whether PtdIns(4,5)P2 regulates FA turnover.<br>
<br>
<strong><em>Methods:</em></strong> MDA-MB-231 cells were co-transfected with a labeling vinculin (or zyxin) and the PLC𝛅1-PH biosensor to visualize FA localization and PtdIns(4,5)P2 in the cell membrane. We also used pharmacological inhibitors to determine the mechanism underlying the changes of PtdIns(4,5)P2 level<br>
during FA turnover and cell migration. Immunostaining, immunoprecipitation, and Western blotting were used to examine the localization and interaction between phospholipase C (PLC)/phosphatidylinositol 3-kinase (PI3K) FA proteins.<br>
<br>
<strong><em>Results: </em></strong>We showed that inhibition of PLC, PI3K significantly reduced the decline of PtdIns(4,5)P2 levels within FA disassembly and the slowdown rate of FA turnover and cell migration. We also showed that the inhibition of enzymes implicated in the downstream pathway of PtdIns(4,5)P2, such as diacylglycerol kinase (DAGK) and protein kinase C (PKC) significantly reduced FA turnover time and the speed of cell migration. Additionally, we demonstrated that PLC but not PI3K interact with FAs. In conclusion,<br>
<br>
<strong><em>Conclusions:</em></strong> This study suggests that dynamical changes of PtdIns(4,5)P2 might regulate FA turnover and facilitate cell migration.</div>
Cell Migration, Focal Adhesion Turnover, MDA-MB-231 Breast Cancer Cell Line,
Ptdins(4,5)P2, PLC, PI3K.
270
281
http://rbmb.net/browse.php?a_code=A-10-749-6&slc_lang=en&sid=1
Dhurgham
Al-Fahad
dhurgham.alfahad@sci.utq.edu.iq
100319475328460012213
100319475328460012213
Yes
Department of Pharmaceutical Sciences, College of Pharmacy University of Thi-Qar, Iraq
Firas
Alyaseen
100319475328460012214
100319475328460012214
No
Department of Pharmaceutical Sciences, College of Pharmacy University of Thi-Qar, Iraq.
Ahmed
Al-Amery
100319475328460012215
100319475328460012215
No
Faculty of Education, Soran University, Erbil, Kurdistan Region, Iraq.
Clementino
Ibeas Bin
100319475328460012216
100319475328460012216
No
Ilumix Biotech Ltd, London, United Kingdom.