| Literature DB >> 30977233 |
Wei Guo1, Henk Roelink1.
Abstract
As a morphogen, Sonic Hedgehog (Shh) mediates signaling at a distance from its sites of synthesis. After secretion, Shh must traverse a distance through the extracellular matrix (ECM) to reach the target cells and activate the Hh response. ECM proteins, in particular, the heparan sulfate proteoglycans (HSPGs) of the glypican family, have both negative and positive effects on Shh signaling, all attributed to their ability to bind Shh. Using mouse embryonic stem cell-derived mosaic tissues with compartments that lack the glycosyltransferases Exostosin1 and Exostosin2, or the HSPG core protein Glypican5, we show that Shh accumulates around its source cells when they are surrounded by cells that have a mutated ECM. This accumulation of Shh is correlated with an increased noncell autonomous Shh response. Our results support a model in which Shh presented on the cell surface accumulates at or near ECM that lacks HSPGs, possibly due to the absence of these Shh sequestering molecules. Stem Cells 2019;37:899-909. © AlphaMed Press 2019.Entities:
Keywords: Cell signaling; Developmental biology; Embryoid bodies; Embryonic stem cells
Mesh:
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Year: 2019 PMID: 30977233 DOI: 10.1002/stem.3018
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277