Cdk5 controls lymphatic vessel development and function by phosphorylation of Foxc2.


Autoria(s): Liebl J.; Zhang S.; Moser M.; Agalarov Y.; Demir C.S.; Hager B.; Bibb J.A.; Adams R.H.; Kiefer F.; Miura N.; Petrova T.V.; Vollmar A.M.; Zahler S.
Data(s)

2015

Resumo

The lymphatic system maintains tissue fluid balance, and dysfunction of lymphatic vessels and valves causes human lymphedema syndromes. Yet, our knowledge of the molecular mechanisms underlying lymphatic vessel development is still limited. Here, we show that cyclin-dependent kinase 5 (Cdk5) is an essential regulator of lymphatic vessel development. Endothelial-specific Cdk5 knockdown causes congenital lymphatic dysfunction and lymphedema due to defective lymphatic vessel patterning and valve formation. We identify the transcription factor Foxc2 as a key substrate of Cdk5 in the lymphatic vasculature, mechanistically linking Cdk5 to lymphatic development and valve morphogenesis. Collectively, our findings show that Cdk5-Foxc2 interaction represents a critical regulator of lymphatic vessel development and the transcriptional network underlying lymphatic vascular remodeling.

Identificador

https://serval.unil.ch/?id=serval:BIB_3B60F81231F4

isbn:2041-1723 (Electronic)

pmid:26027726

doi:10.1038/ncomms8274

isiid:000357170800001

Idioma(s)

en

Fonte

Nature Communications, vol. 6, pp. 7274

Palavras-Chave #Animals; Cyclin-Dependent Kinase 5/genetics; Cyclin-Dependent Kinase 5/metabolism; Endothelial Cells/cytology; Endothelial Cells/metabolism; Forkhead Transcription Factors/genetics; Forkhead Transcription Factors/metabolism; Human Umbilical Vein Endothelial Cells; Humans; Lymphangiogenesis/genetics; Lymphatic Vessels/metabolism; Lymphatic Vessels/pathology; Mice; Mice, Knockout; Phosphorylation; Real-Time Polymerase Chain Reaction; Stress, Mechanical
Tipo

info:eu-repo/semantics/article

article