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清道夫受体内吞作用控制气道顶膜形态发生。

Scavenger receptor endocytosis controls apical membrane morphogenesis in the airways.

机构信息

Science for Life Laboratory, Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden.

IMBA - Institute of Molecular Biotechnology, Austrian Academy of Sciences, Vienna, Austria.

出版信息

Elife. 2023 Sep 14;12:e84974. doi: 10.7554/eLife.84974.

DOI:10.7554/eLife.84974
PMID:37706489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10564452/
Abstract

The acquisition of distinct branch sizes and shapes is a central aspect in tubular organ morphogenesis and function. In the airway tree, the interplay of apical extracellular matrix (ECM) components with the underlying membrane and cytoskeleton controls tube elongation, but the link between ECM composition with apical membrane morphogenesis and tube size regulation is elusive. Here, we characterized Emp (epithelial membrane protein), a CD36 homolog belonging to the scavenger receptor class B protein family. mutant embryos fail to internalize the luminal chitin deacetylases Serp and Verm at the final stages of airway maturation and die at hatching with liquid filled airways. Emp localizes in apical epithelial membranes and shows cargo selectivity for LDLr-domain containing proteins. mutants also display over elongated tracheal tubes with increased levels of the apical proteins Crb, DE-cad, and phosphorylated Src (p-Src). We show that Emp associates with and organizes the βH-Spectrin cytoskeleton and is itself confined by apical F-actin bundles. Overexpression or loss of its cargo protein Serp lead to abnormal apical accumulations of Emp and perturbations in p-Src levels. We propose that during morphogenesis, Emp senses and responds to luminal cargo levels by initiating apical membrane endocytosis along the longitudinal tube axis and thereby restricts airway elongation.

摘要

获得不同的分支大小和形状是管状器官形态发生和功能的一个核心方面。在气道树中,顶端细胞外基质(ECM)成分与下面的膜和细胞骨架的相互作用控制着管的伸长,但 ECM 组成与顶端膜形态发生和管大小调节之间的联系还不清楚。在这里,我们描述了 Emp(上皮膜蛋白),它是 CD36 同源物,属于清道夫受体 B 蛋白家族。 Emp 突变体胚胎在气道成熟的最后阶段不能内化腔内几丁质去乙酰酶 Serp 和 Verm,并且在孵化时死于充满液体的气道。Emp 定位于顶端上皮膜中,并且对 LDLr 结构域包含的蛋白质具有货物选择性。 Emp 突变体也显示出气管管过度伸长,顶端蛋白 Crb、DE-cad 和磷酸化 Src(p-Src)水平增加。我们表明,Emp 与βH- spectrin 细胞骨架结合并将其自身组织起来,并且自身受到顶端 F-肌动蛋白束的限制。其货物蛋白 Serp 的过表达或缺失导致 Emp 的异常顶端积累和 p-Src 水平的扰动。我们提出,在形态发生过程中,Emp 通过沿纵向管轴起始顶端膜内吞作用来感知和响应腔内货物水平,从而限制气道伸长。

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