Hippo-YAP/TAZ signaling in angiogenesis

被引:69
作者
Park, Jeong Ae [1 ,2 ]
Kwon, Young-Guen [1 ,2 ]
机构
[1] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Biochem, Seoul 03722, South Korea
[2] Yonsei Univ, PLUS BK21, Initiat Biol Funct & Syst, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
VEGF; Vascular development; Endothelial cell junction; AmotL1/2; Hecw2; ENDOTHELIAL-CELL MIGRATION; YES-ASSOCIATED PROTEIN; VE-CADHERIN; REGULATES ANGIOGENESIS; TRANSCRIPTION FACTOR; YAP; STABILITY; JUNCTIONS; PATHWAY; WNT;
D O I
10.5483/BMBRep.2018.51.3.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Angiogenesis is a complex, multistep process involving dynamic changes in endothelial cell (EC) shapes and behaviors, especially in specialized cell types such as tip cells (with active filopodial extensions), stalk cells (with less motility) and phalanx cells (with stable junction connections). The Hippo-Yes-associated protein (YAP)/transcription activator with PDZ binding motif (TAZ) signaling plays a critical role in development, regeneration and organ size by regulating cell-cell contact and actin cytoskeleton dynamics. Recently, with the finding that YAP is expressed in the front edge of the developing retinal vessels, Hippo-YAP/TAZ signaling has emerged as a new pathway for blood vessel development. Intriguingly, the LATS1/2-mediated angiomotin (AMOT) family and YAP/TAZ activities contribute to EC shapes and behaviors by spatiotemporally modulating actin cytoskeleton dynamics and EC junction stability. Herein, we summarize the recent understanding of the role of Hippo-YAP/TAZ signaling in the processes of EC sprouting and junction maturation in angiogenesis.
引用
收藏
页码:157 / 162
页数:6
相关论文
共 49 条
[1]   Angiomotin regulates endothelial cell migration during embryonic angiogenesis [J].
Aase, Karin ;
Ernkvist, Mira ;
Ebarasi, Lwaki ;
Jakobsson, Lars ;
Majumdar, Arindam ;
Yi, Chunling ;
Birot, Olivier ;
Ming, Yue ;
Kvanta, Anders ;
Edholm, Dan ;
Aspenstrom, Pontus ;
Kissil, Joseph ;
Claesson-Welsh, Lena ;
Shimono, Akihiko ;
Holmgren, Lars .
GENES & DEVELOPMENT, 2007, 21 (16) :2055-2068
[2]   Cdc42 is required for cytoskeletal support of endothelial cell adhesion during blood vessel formation in mice [J].
Barry, David M. ;
Xu, Ke ;
Meadows, Stryder M. ;
Zheng, Yi ;
Norden, Pieter R. ;
Davis, George E. ;
Cleaver, Ondine .
DEVELOPMENT, 2015, 142 (17) :3058-+
[3]   Akt phosphorylates the Yes-associated protein, YAP, to induce interaction with 14-3-3 and attenuation of p73-mediated apoptosis [J].
Basu, S ;
Totty, NF ;
Irwin, MS ;
Sudol, M ;
Downward, J .
MOLECULAR CELL, 2003, 11 (01) :11-23
[4]   The role of differential VE-cadherin dynamics in cell rearrangement during angiogenesis [J].
Bentley, Katie ;
Franco, Claudio Areias ;
Philippides, Andrew ;
Blanco, Raquel ;
Dierkes, Martina ;
Gebala, Veronique ;
Stanchi, Fabio ;
Jones, Martin ;
Aspalter, Irene M. ;
Cagna, Guiseppe ;
Westrom, Simone ;
Claesson-Welsh, Lena ;
Vestweber, Dietmar ;
Gerhardt, Holger .
NATURE CELL BIOLOGY, 2014, 16 (04) :309-+
[5]   Crossroads of Wnt and Hippo in epithelial tissues [J].
Bernascone, Ilenia ;
Martin-Belmonte, Fernando .
TRENDS IN CELL BIOLOGY, 2013, 23 (08) :380-389
[6]   Transcription factor Erg regulates angiogenesis and endothelial apoptosis through VE-cadherin [J].
Birdsey, Graeme M. ;
Dryden, Nicola H. ;
Amsellem, Valerie ;
Gebhardt, Frank ;
Sahnan, Kapil ;
Haskard, Dorian O. ;
Dejana, Elisabetta ;
Mason, Justin C. ;
Randi, Anna M. .
BLOOD, 2008, 111 (07) :3498-3506
[7]   Akt1 regulates pathological angiogenesis, vascular maturation and permeability in vivo [J].
Chen, JH ;
Somanath, PR ;
Razorenova, O ;
Chen, WS ;
Hay, N ;
Bornstein, P ;
Byzova, TV .
NATURE MEDICINE, 2005, 11 (11) :1188-1196
[8]   Yes-associated protein regulates endothelial cell contact-mediated expression of angiopoietin-2 [J].
Choi, Hyun-Jung ;
Zhang, Haiying ;
Park, Hongryeol ;
Choi, Kyu-Sung ;
Lee, Heon-Woo ;
Agrawal, Vijayendra ;
Kim, Young-Myeong ;
Kwon, Young-Guen .
NATURE COMMUNICATIONS, 2015, 6
[9]   The endothelial E3 ligase HECW2 promotes endothelial cell junctions by increasing AMOTL1 protein stability via K63-linked ubiquitination [J].
Choi, Kyu-Sung ;
Choi, Hyun-Jung ;
Lee, Jin-Kyu ;
Im, Suhjean ;
Zhang, Haiying ;
Jeong, Yoonjeong ;
Park, Jeong Ae ;
Lee, In-Kyu ;
Kim, Young-Myeong ;
Kwon, Young-Guen .
CELLULAR SIGNALLING, 2016, 28 (11) :1642-1651
[10]   The Amot/Patj/Syx signaling complex spatially controls RhoA GTPase activity in migrating endothelial cells [J].
Ernkvist, Mira ;
Persson, Nathalie Luna ;
Audebert, Stephane ;
Lecine, Patrick ;
Sinha, Indranil ;
Liu, Miaoliang ;
Schlueter, Marc ;
Horowitz, Arie ;
Aase, Karin ;
Weide, Thomas ;
Borg, Jean-Paul ;
Majumdar, Arindam ;
Holmgren, Lars .
BLOOD, 2009, 113 (01) :244-253