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聚糖蛋白 5 缺失促进长距离 Sonic Hedgehog 信号转导。

Loss of the Heparan Sulfate Proteoglycan Glypican5 Facilitates Long-Range Sonic Hedgehog Signaling.

机构信息

Department of Molecular and Cell Biology, University of California at Berkeley, Berkeley, California, USA.

出版信息

Stem Cells. 2019 Jul;37(7):899-909. doi: 10.1002/stem.3018. Epub 2019 May 13.

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.

摘要

作为一种形态发生素,Sonic Hedgehog(Shh)在远离其合成部位的地方进行信号传递。分泌后,Shh 必须穿过细胞外基质(ECM)到达靶细胞并激活 Hh 反应。细胞外基质蛋白,特别是糖胺聚糖蛋白聚糖(HSPGs)家族的 HSPGs,对 Shh 信号具有正反两方面的影响,这都归因于它们结合 Shh 的能力。使用缺乏糖基转移酶 Exostosin1 和 Exostosin2 或 HSPG 核心蛋白 Glypican5 的小鼠胚胎干细胞衍生的镶嵌组织,我们表明 Shh 在其来源细胞被周围具有突变 ECM 的细胞包围时会在其周围积累。这种 Shh 的积累与非细胞自主 Shh 反应的增加相关。我们的结果支持这样一种模型,即细胞表面呈现的 Shh 会在缺乏 HSPG 的 ECM 上或附近积累,这可能是由于这些 Shh 隔离分子的缺失。干细胞 2019;37:899-909。

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