Wnt信号通路
受体
细胞生物学
硫酸乙酰肝素
信号转导
生物
配体(生物化学)
化学
生物化学
糖胺聚糖
作者
Ramin Dubey,Peter van Kerkhof,Ingrid Jordens,Tomas Malinauskas,Ganesh V. Pusapati,Joseph K McKenna,Dan Li,Jan E. Carette,Mitchell Ho,Christian Siebold,Madelon M. Maurice,Andres M. Lebensohn,Rajat Rohatgi
出处
期刊:eLife
[eLife Sciences Publications, Ltd.]
日期:2020-05-20
卷期号:9
被引量:33
摘要
R-spondins (RSPOs) amplify WNT signaling during development and regenerative responses. We previously demonstrated that RSPOs 2 and 3 potentiate WNT/β-catenin signaling in cells lacking leucine-rich repeat-containing G-protein coupled receptors (LGRs) 4, 5 and 6 (Lebensohn and Rohatgi, 2018). We now show that heparan sulfate proteoglycans (HSPGs) act as alternative co-receptors for RSPO3 using a combination of ligand mutagenesis and ligand engineering. Mutations in RSPO3 residues predicted to contact HSPGs impair its signaling capacity. Conversely, the HSPG-binding domains of RSPO3 can be entirely replaced with an antibody that recognizes heparan sulfate (HS) chains attached to multiple HSPGs without diminishing WNT-potentiating activity in cultured cells and intestinal organoids. A genome-wide screen for mediators of RSPO3 signaling in cells lacking LGRs 4, 5 and 6 failed to reveal other receptors. We conclude that HSPGs are RSPO co-receptors that potentiate WNT signaling in the presence and absence of LGRs.
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