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本文引用的文献

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SPINT2 inhibits proteases involved in activation of both influenza viruses and metapneumoviruses.SPINT2 抑制了两种病毒(流感病毒和肺炎支原体病毒)激活过程中涉及的蛋白酶。
Virology. 2020 Apr;543:43-53. doi: 10.1016/j.virol.2020.01.004. Epub 2020 Jan 7.
2
Regulating ENaC's gate.调节 ENaC 的门控。
Am J Physiol Cell Physiol. 2020 Jan 1;318(1):C150-C162. doi: 10.1152/ajpcell.00418.2019. Epub 2019 Nov 13.
3
Matriptase drives early-onset intestinal failure in a mouse model of congenital tufting enteropathy.丝氨酸蛋白酶 Matriptase 驱动先天性簇状肠病小鼠模型的早发性肠衰竭。
Development. 2019 Nov 18;146(22):dev183392. doi: 10.1242/dev.183392.
4
Cell surface-anchored serine proteases in cancer progression and metastasis.细胞表面锚定的丝氨酸蛋白酶在癌症进展和转移中的作用。
Cancer Metastasis Rev. 2019 Sep;38(3):357-387. doi: 10.1007/s10555-019-09811-7.
5
Iterative, multiplexed CRISPR-mediated gene editing for functional analysis of complex protease gene clusters.迭代、多重 CRISPR 介导的基因编辑用于复杂蛋白酶基因簇的功能分析。
J Biol Chem. 2019 Nov 1;294(44):15987-15996. doi: 10.1074/jbc.RA119.009773. Epub 2019 Sep 9.
6
Hepsin-mediated Processing of Uromodulin is Crucial for Salt-sensitivity and Thick Ascending Limb Homeostasis.尿调蛋白的 Hepsin 介导加工对于盐敏感性和厚升支的稳态至关重要。
Sci Rep. 2019 Aug 23;9(1):12287. doi: 10.1038/s41598-019-48300-3.
7
Defective Tmprss3-Associated Hair Cell Degeneration in Inner Ear Organoids.内耳类器官中 Tmprss3 相关的毛细胞变性缺陷。
Stem Cell Reports. 2019 Jul 9;13(1):147-162. doi: 10.1016/j.stemcr.2019.05.014. Epub 2019 Jun 13.
8
Tmprss2 knock-out mice are resistant to H10 influenza A virus pathogenesis.Tmprss2 敲除小鼠对 H10 流感 A 病毒发病机制具有抗性。
J Gen Virol. 2019 Jul;100(7):1073-1078. doi: 10.1099/jgv.0.001274. Epub 2019 May 17.
9
Hepatocyte growth factor activator inhibitor-2 stabilizes Epcam and maintains epithelial organization in the mouse intestine.肝细胞生长因子激活物抑制剂-2稳定 EpCAM 并维持小鼠肠道的上皮组织。
Commun Biol. 2019 Jan 4;2:11. doi: 10.1038/s42003-018-0255-8. eCollection 2019.
10
Conserved function of the matriptase-prostasin proteolytic cascade during epithelial morphogenesis.上皮形态发生过程中组织蛋白酶谱蛋白酶原蛋白水解级联的保守功能。
PLoS Genet. 2019 Jan 2;15(1):e1007882. doi: 10.1371/journal.pgen.1007882. eCollection 2019 Jan.

膜锚定丝氨酸蛋白酶作为上皮功能的调节剂。

Membrane-anchored serine proteases as regulators of epithelial function.

机构信息

Proteases and Tissue Remodeling Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, U.S.A.

出版信息

Biochem Soc Trans. 2020 Apr 29;48(2):517-528. doi: 10.1042/BST20190675.

DOI:10.1042/BST20190675
PMID:32196551
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9869603/
Abstract

Cleavage of proteins in the extracellular milieu, including hormones, growth factors and their receptors, ion channels, and various cell adhesion and extracellular matrix molecules, plays a key role in the regulation of cell behavior. Among more than 500 proteolytic enzymes encoded by mammalian genomes, membrane-anchored serine proteases (MASPs), which are expressed on the surface of epithelial cells of all major organs, are excellently suited to mediate signal transduction across the epithelia and are increasingly being recognized as important regulators of epithelial development, function, and disease [ 1-3]. In this minireview, we summarize current knowledge of the in vivo roles of MASPs in acquisition and maintenance of some of the defining functions of epithelial tissues, such as barrier formation, ion transport, and sensory perception.

摘要

细胞外环境中蛋白质的裂解在细胞行为的调节中起着关键作用,包括激素、生长因子及其受体、离子通道和各种细胞黏附和细胞外基质分子。在哺乳动物基因组编码的 500 多种蛋白水解酶中,膜锚定丝氨酸蛋白酶(MASPs)表达于所有主要器官的上皮细胞表面,非常适合介导上皮细胞间的信号转导,并且越来越被认为是上皮细胞发育、功能和疾病的重要调节因子[1-3]。在这篇综述中,我们总结了 MASPs 在体内获得和维持上皮组织某些特有功能(如形成屏障、离子转运和感觉感知)中的作用的最新知识。