CELSR1 is a positive regulator of endothelial cell migration and angiogenesis

التفاصيل البيبلوغرافية
العنوان: CELSR1 is a positive regulator of endothelial cell migration and angiogenesis
المؤلفون: Cong-Xia Lu, Qi-Lin Ma, Yi-Hong Zhan, Ning Wang, Cen Yue, Xiao-Rong Zhang, Qi-Cong Luo, Nai-An Xiao
المصدر: Biochemistry (Moscow). 81:591-599
بيانات النشر: Pleiades Publishing Ltd, 2016.
سنة النشر: 2016
مصطلحات موضوعية: 0301 basic medicine, Angiogenesis, Cell, Neovascularization, Physiologic, Biology, Biochemistry, Cell Line, Small hairpin RNA, 03 medical and health sciences, Cell Movement, Epidermal growth factor, Human Umbilical Vein Endothelial Cells, medicine, Humans, RNA, Small Interfering, Cell Proliferation, Tube formation, Cell growth, Wnt signaling pathway, Endothelial Cells, General Medicine, Cadherins, Cell biology, Endothelial stem cell, 030104 developmental biology, medicine.anatomical_structure, RNA Interference, Plasmids
الوصف: Cadherin is an epidermal growth factor and laminin-G seven-pass G-type receptor 1 (CELSR1) is a key component of the noncanonical Wnt/planar cell polarity (PCP) pathway that critically regulates endothelial cell proliferation and angiogenesis. In this study, we examined the biological significance of CELSR1 in endothelial cell migration and angiogenesis. For this, we applied both gain-of-function and loss-of-function approaches. To increase the endogenous expression of CELSR1, we used the transcription activator-like effector (TALE) technology and constructed an artificial TALE-VP64 activator. To knock down the expression of CELSR1, we generated lentivirus containing short hairpin RNA sequences targeting different regions of CELSR1 mRNA. Following up- or down-regulation of CELSR1 in human aortic endothelial cells (HAEC), we assessed in vitro cell proliferation by MTT assay, migration by scratch and transwell migration assays, and angiogenesis by tube formation analysis. We found that CELSR1 was endogenously expressed in human umbilical vein endothelial cells (HUVEC) and HAEC. When focusing on HAEC, we found that upregulating CELSR1 expression significantly promoted cell growth, while knocking down CELSR1 inhibited the growth (p < 0.05). Using both scratch and transwell migration assays, we observed a positive correlation between CELSR1 expression and cell migratory capability. In addition, CELSR1 upregulation led to higher levels of tube formation in HAEC, while downregulating CELSR1 expression decreased tube formation (p < 0.05). Mechanistically, CELSR1-regulated migration and tube formation was mediated through disheveled segment polarity protein 3 (Dvl3). In conclusion, CELSR1 plays an important role in regulating multiple phenotypes of endothelial cells, including proliferation, migration, and formation of capillary-like structures.
تدمد: 1608-3040
0006-2979
DOI: 10.1134/s0006297916060055
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0d161db9c3475d2f53d4de913bd4068
https://doi.org/10.1134/s0006297916060055
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....b0d161db9c3475d2f53d4de913bd4068
قاعدة البيانات: OpenAIRE
الوصف
تدمد:16083040
00062979
DOI:10.1134/s0006297916060055