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Tsg101 对于建立和维持小鼠视网膜色素上皮细胞极性是必要的。

Tsg101 Is Necessary for the Establishment and Maintenance of Mouse Retinal Pigment Epithelial Cell Polarity.

机构信息

Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Korea.

These authors contributed equally to this work.

出版信息

Mol Cells. 2021 Mar 31;44(3):168-178. doi: 10.14348/molcells.2021.0027.

DOI:10.14348/molcells.2021.0027
PMID:33795534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8019596/
Abstract

The retinal pigment epithelium (RPE) forms a monolayer sheet separating the retina and choroid in vertebrate eyes. The polarized nature of RPE is maintained by distributing membrane proteins differentially along apico-basal axis. We found the distributions of these proteins differ in embryonic, post-natal, and mature mouse RPE, suggesting developmental regulation of protein trafficking. Thus, we deleted tumor 101 (), a key component of endosomal sorting complexes required for transport (ESCRT), in embryonic and mature RPE to determine whether ESCRT-mediated endocytic protein trafficking correlated with the establishment and maintenance of RPE polarity. Loss of severely disturbed the polarity of RPE, which forms irregular aggregates exhibiting non-polarized distribution of cell adhesion proteins and activation of epidermal growth factor receptor signaling. These findings suggest that ESCRT-mediated protein trafficking is essential for the development and maintenance of RPE cell polarity.

摘要

视网膜色素上皮 (RPE) 在脊椎动物的眼睛中形成一层分离视网膜和脉络膜的单层薄片。RPE 的极化性质通过在顶-基底轴上差异分布膜蛋白来维持。我们发现这些蛋白质在胚胎期、出生后和成熟的小鼠 RPE 中的分布不同,这表明蛋白质运输的发育调控。因此,我们在胚胎期和成熟的 RPE 中删除了肿瘤 101(),这是内体分选复合物必需的运输 (ESCRT) 的关键组成部分,以确定 ESCRT 介导的内吞蛋白运输是否与 RPE 极性的建立和维持相关。缺失严重扰乱了 RPE 的极性,RPE 形成不规则聚集,表现出细胞粘附蛋白的非极化分布和表皮生长因子受体信号的激活。这些发现表明 ESCRT 介导的蛋白质运输对于 RPE 细胞极性的发育和维持至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/61cc23356bec/molce-44-3-168-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/aea61770fb32/molce-44-3-168-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/661281619233/molce-44-3-168-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/867c8d5f334c/molce-44-3-168-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/1928c63de708/molce-44-3-168-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/8643c872d291/molce-44-3-168-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/61cc23356bec/molce-44-3-168-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/aea61770fb32/molce-44-3-168-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/661281619233/molce-44-3-168-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/867c8d5f334c/molce-44-3-168-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/1928c63de708/molce-44-3-168-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/8643c872d291/molce-44-3-168-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b4/8019596/61cc23356bec/molce-44-3-168-f6.jpg

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