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胶质细胞源性神经营养因子(GFL)受体组分的质膜定位:受体相互作用的枢纽

Plasma membrane localization of the GFL receptor components: a nexus for receptor crosstalk.

作者信息

Donnelly Christopher R, Pierchala Brian A

机构信息

Department of Anesthesiology Center for Translational Pain Medicine, Duke University Medical Center, Durham, NC, 27710, USA.

Department of Anatomy, Cell Biology & Physiology, Stark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.

出版信息

Cell Tissue Res. 2020 Oct;382(1):57-64. doi: 10.1007/s00441-020-03235-4. Epub 2020 Aug 7.

Abstract

The glial cell line-derived neurotrophic factor (GDNF) family ligands (GFLs) comprise a group of four homologous and potent growth factors that includes GDNF, neurturin (NRTN), artemin (ARTN), and persephin (PSPN). The survival, growth, and mitotic activities of the GFLs are conveyed by a single receptor tyrosine kinase, Ret. The GFLs do not bind directly to Ret in order to activate it, and instead bind with high affinity to glycerophosphatidylinositol (GPI)-anchored coreceptors called the GDNF family receptor-αs (GFRαs). Several mechanisms have recently been identified that influence the trafficking of Ret and GFRαs in and out of the plasma membrane, thereby affecting their availability for ligand binding, as well as their levels by targeting to degradative pathways. This review describes these mechanisms and their powerful effects on GFL signaling and function. We also describe the recent discovery that p75 and Ret form a signaling complex, also regulated by plasma membrane shuttling, that either enhances GFL survival signals or p75 pro-apoptotic signals, dependent on the cellular context.

摘要

胶质细胞系源性神经营养因子(GDNF)家族配体(GFLs)由四种同源且强效的生长因子组成,包括GDNF、神经营养素(NRTN)、艺术蛋白(ARTN)和persephin(PSPN)。GFLs的存活、生长和有丝分裂活性由单一的受体酪氨酸激酶Ret介导。GFLs并不直接与Ret结合以激活它,而是与一种称为GDNF家族受体α(GFRαs)的甘油磷脂酰肌醇(GPI)锚定共受体高亲和力结合。最近已确定了几种机制,这些机制影响Ret和GFRαs进出质膜的运输,从而影响它们与配体结合的可用性,以及通过靶向降解途径来影响它们的水平。本综述描述了这些机制及其对GFL信号传导和功能的强大影响。我们还描述了最近的一项发现,即p75和Ret形成一种信号复合物,该复合物也受质膜穿梭调节,根据细胞环境,它要么增强GFL存活信号,要么增强p75促凋亡信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36db/7529631/521d9ef365a4/441_2020_3235_Fig1_HTML.jpg

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