淋巴系统
钙粘蛋白
粘合连接
淋巴管内皮
细胞生物学
淋巴管
下调和上调
生物
淋巴水肿
蛋白激酶B
淋巴管新生
癌症研究
VE钙粘蛋白
信号转导
免疫学
癌症
细胞
基因
乳腺癌
遗传学
转移
作者
Ying Yang,Boksik Cha,Zeinab Y. Motawe,R. Sathish Srinivasan,Joshua P. Scallan
出处
期刊:Cell Reports
[Cell Press]
日期:2019-08-01
卷期号:28 (9): 2397-2412.e4
被引量:93
标识
DOI:10.1016/j.celrep.2019.07.072
摘要
The lymphatic vasculature requires intraluminal valves to maintain forward lymph flow. Lymphatic valves form and are constantly maintained by oscillatory fluid flow throughout life, yet the earliest steps of how lymphatic endothelial cells are able to respond to fluid shear stress remain unknown. Here, we show that the adherens junction protein VE-cadherin is required for the upregulation of valve-specific transcription factors. Conditional deletion of VE-cadherin in vivo prevented valve formation in the embryo and caused postnatal regression of nearly all lymphatic valves in multiple tissues. Since VE-cadherin is known to signal through β-catenin and the VEGFR/AKT pathway, each pathway was probed. Expression of a constitutively active β-catenin mutant or direct pharmacologic activation of AKT in vivo significantly rescued valve regression in the VE-cadherin-deficient lymphatic vessels. In conclusion, VE-cadherin-dependent signaling is required for lymphatic valve formation and maintenance and therapies to augment downstream pathways hold potential to treat lymphedema in patients.
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