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人原代表皮角质形成细胞作为分析半胱天冬酶-1依赖性非常规蛋白质分泌的工具

Human Primary Keratinocytes as a Tool for the Analysis of Caspase-1-Dependent Unconventional Protein Secretion.

作者信息

Strittmatter Gerhard E, Garstkiewicz Martha, Sand Jennifer, Grossi Serena, Beer Hans-Dietmar

机构信息

Department of Dermatology, University Hospital Zurich, University Zurich, Gloriastrasse 31, CH-8091, Zurich, Switzerland.

出版信息

Methods Mol Biol. 2016;1459:135-47. doi: 10.1007/978-1-4939-3804-9_9.

Abstract

Inflammasomes comprise a group of protein complexes, which activate the protease caspase-1 upon sensing a variety of stress factors. Active caspase-1 in turn cleaves and thereby activates the pro-inflammatory cytokines prointerleukin (IL)-1β and -18, and induces unconventional protein secretion (UPS) of mature IL-1β, IL-18, as well as of many other proteins involved in and required for induction of inflammation. Human primary keratinocytes (HPKs) represent epithelial cells able to activate caspase-1 in an inflammasome-dependent manner upon irradiation with a physiological dose of ultraviolet B (UVB) light. Here, we describe the isolation of keratinocytes from human skin, their cultivation, and induction of caspase-1-dependent UPS upon UVB irradiation as well as its siRNA- and chemical-mediated inhibition. In contrast to inflammasome activation of professional immune cells, UVB-irradiated HPKs represent a robust and physiological cell culture system for the analysis of UPS induced by active caspase-1.

摘要

炎性小体由一组蛋白质复合物组成,它们在感知各种应激因素时会激活蛋白酶caspase-1。激活的caspase-1反过来会切割并激活促炎细胞因子前白细胞介素(IL)-1β和-18,并诱导成熟IL-1β、IL-18以及许多其他参与炎症诱导并为炎症诱导所必需的蛋白质的非常规蛋白质分泌(UPS)。人原代表皮细胞,在生理剂量的紫外线B(UVB)照射后,能够以炎性小体依赖的方式激活caspase-1。在此,我们描述了从人皮肤中分离角质形成细胞、其培养方法,以及UVB照射后caspase-1依赖性UPS的诱导及其siRNA和化学介导的抑制。与专业免疫细胞的炎性小体激活不同,UVB照射的人原代表皮细胞是用于分析由活性caspase-1诱导的UPS的强大且生理的细胞培养系统。

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