
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. [BMB Reports 2018; 51(3): 157-162].
Neovascularization, Pathologic, Tumor Suppressor Proteins, Nuclear Proteins, Cell Cycle Proteins, Protein Serine-Threonine Kinases, Invited Mini Review, Animals, Humans, Hippo Signaling Pathway, Acyltransferases, Signal Transduction, Transcription Factors
Neovascularization, Pathologic, Tumor Suppressor Proteins, Nuclear Proteins, Cell Cycle Proteins, Protein Serine-Threonine Kinases, Invited Mini Review, Animals, Humans, Hippo Signaling Pathway, Acyltransferases, Signal Transduction, Transcription Factors
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