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转化生长因子-β受体的调控

Regulation of TGF-β Receptors.

作者信息

Budi Erine H, Xu Jian, Derynck Rik

机构信息

Department of Cell and Tissue Biology, Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Programs in Cell Biology, and Developmental and Stem Cell Biology, University of California, San Francisco, CA, USA.

Center for Craniofacial Molecular Biology, Ostrow School of Dentistry of USC, University of Southern California, Los Angeles, CA, USA.

出版信息

Methods Mol Biol. 2016;1344:1-33. doi: 10.1007/978-1-4939-2966-5_1.

Abstract

In cells responding to extracellular polypeptide ligands, regulatory mechanisms at the level of cell surface receptors are increasingly seen to define the nature of the ligand-induced signaling responses. Processes that govern the levels of receptors at the plasma membrane, including posttranslational modifications, are crucial to ensure receptor function and specify the downstream signals. Indeed, extracellular posttranslational modifications of the receptors help define stability and ligand binding, while intracellular modifications mediate interactions with signaling mediators and accessory proteins that help define the nature of the signaling response. The use of various molecular biology and biochemistry techniques, based on chemical crosslinking, e.g., biotin or radioactive labeling, immunofluorescence to label membrane receptors and flow cytometry, allows for quantification of changes of cell surface receptor presentation. Here, we discuss recent progress in our understanding of the regulation of TGF-β receptors, i.e., the type I (TβRI) and type II (TβRII) TGF-β receptors, and describe basic methods to identify and quantify TGF-β cell surface receptors.

摘要

在对细胞外多肽配体作出反应的细胞中,越来越多的证据表明,细胞表面受体水平的调节机制决定了配体诱导的信号反应的性质。控制质膜上受体水平的过程,包括翻译后修饰,对于确保受体功能和确定下游信号至关重要。实际上,受体的细胞外翻译后修饰有助于确定稳定性和配体结合,而细胞内修饰介导与信号介质和辅助蛋白的相互作用,这些相互作用有助于确定信号反应的性质。基于化学交联(如生物素或放射性标记)、免疫荧光标记膜受体和流式细胞术等各种分子生物学和生物化学技术,可用于定量细胞表面受体表达的变化。在此,我们讨论了我们对转化生长因子-β(TGF-β)受体(即I型(TβRI)和II型(TβRII)TGF-β受体)调节的最新认识,并描述了鉴定和定量TGF-β细胞表面受体的基本方法。

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