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填补空白:硫酸乙酰肝素和Scube2在产生细胞表面组装音猬因子释放复合物。

Bridging the gap: heparan sulfate and Scube2 assemble Sonic hedgehog release complexes at the surface of producing cells.

作者信息

Jakobs P, Schulz P, Ortmann C, Schürmann S, Exner S, Rebollido-Rios R, Dreier R, Seidler D G, Grobe K

机构信息

Institute for Physiological Chemistry and Pathobiochemistry and Cells-in-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, Waldeyerstr. 15, D-48149 Münster, Germany.

Center for Medical Biotechnology#, University of Duisburg-Essen, 45117 Essen, Germany.

出版信息

Sci Rep. 2016 May 20;6:26435. doi: 10.1038/srep26435.

Abstract

Decision making in cellular ensembles requires the dynamic release of signaling molecules from the producing cells into the extracellular compartment. One important example of molecules that require regulated release in order to signal over several cell diameters is the Hedgehog (Hh) family, because all Hhs are synthesized as dual-lipidated proteins that firmly tether to the outer membrane leaflet of the cell that produces them. Factors for the release of the vertebrate Hh family member Sonic Hedgehog (Shh) include cell-surface sheddases that remove the lipidated terminal peptides, as well as the soluble glycoprotein Scube2 that cell-nonautonomously enhances this process. This raises the question of how soluble Scube2 is recruited to cell-bound Shh substrates to regulate their turnover. We hypothesized that heparan sulfate (HS) proteoglycans (HSPGs) on the producing cell surface may play this role. In this work, we confirm that HSPGs enrich Scube2 at the surface of Shh-producing cells and that Scube2-regulated proteolytic Shh processing and release depends on specific HS. This finding indicates that HSPGs act as cell-surface assembly and storage platforms for Shh substrates and for protein factors required for their release, making HSPGs critical decision makers for Scube2-dependent Shh signaling from the surface of producing cells.

摘要

细胞群体中的决策需要信号分子从产生细胞动态释放到细胞外区域。需要调控释放以便在几个细胞直径范围内进行信号传导的分子的一个重要例子是刺猬蛋白(Hh)家族,因为所有Hh蛋白都是作为双脂化蛋白合成的,它们牢固地锚定在产生它们的细胞的外膜小叶上。脊椎动物Hh家族成员音猬因子(Shh)释放的因素包括去除脂化末端肽的细胞表面脱落酶,以及非细胞自主增强这一过程的可溶性糖蛋白Scube2。这就提出了一个问题,即可溶性Scube2是如何被招募到细胞结合的Shh底物上以调节它们的周转的。我们假设产生细胞表面的硫酸乙酰肝素(HS)蛋白聚糖(HSPG)可能起这个作用。在这项工作中,我们证实HSPG在产生Shh的细胞表面富集Scube2,并且Scube2调节的蛋白水解性Shh加工和释放依赖于特定的HS。这一发现表明,HSPG作为Shh底物及其释放所需蛋白质因子的细胞表面组装和储存平台,使HSPG成为产生细胞表面Scube2依赖性Shh信号传导的关键决策者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edb4/4873810/e69037c897fa/srep26435-f1.jpg

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