Caspase-8 modulates physiological and pathological angiogenesis during retina development
Details
Publication Year 2019-12-02,Volume 129,Issue #12,Page 5092-5107
Journal Title
Journal of Clinical Investigation
Publication Type
Journal Article
Abstract
During developmental angiogenesis, blood vessels grow and remodel to ultimately build a hierarchical vascular network. Whether, how, cell death signaling molecules contribute to blood vessel formation is still not well understood. Caspase-8 (Casp-8), a key protease in the extrinsic cell death-signaling pathway, regulates cell death via both apoptosis and necroptosis. Here, we show that expression of Casp-8 in endothelial cells (ECs) is required for proper postnatal retina angiogenesis. EC-specific Casp-8-KO pups (Casp-8ECKO) showed reduced retina angiogenesis, as the loss of Casp-8 reduced EC proliferation, sprouting, and migration independently of its cell death function. Instead, the loss of Casp-8 caused hyperactivation of p38 MAPK downstream of receptor-interacting serine/threonine protein kinase 3 (RIPK3) and destabilization of vascular endothelial cadherin (VE-cadherin) at EC junctions. In a mouse model of oxygen-induced retinopathy (OIR) resembling retinopathy of prematurity (ROP), loss of Casp-8 in ECs was beneficial, as pathological neovascularization was reduced in Casp-8ECKO pups. Taking these data together, we show that Casp-8 acts in a cell death-independent manner in ECs to regulate the formation of the retina vasculature and that Casp-8 in ECs is mechanistically involved in the pathophysiology of ROP.
Publisher
Am Soc Clin Invest
Research Division(s)
Epigenetics And Development
PubMed ID
31454332
NHMRC Grants
NHMRC/1125536
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2019-12-16 02:49:02
Last Modified: 2019-12-16 03:05:26
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