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代谢型谷氨酸受体 5(mGluR5)的组成性内化和循环。

Constitutive internalization and recycling of metabotropic glutamate receptor 5 (mGluR5).

机构信息

Department of Biological Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Knowledge City, Sector-81, SAS Nagar, 140306 Punjab, India.

出版信息

Biochem Biophys Res Commun. 2012 Oct 12;427(1):185-90. doi: 10.1016/j.bbrc.2012.09.040. Epub 2012 Sep 17.

Abstract

Ligand-dependent and ligand-independent endocytic trafficking of G-protein coupled receptors (GPCRs) is critical for accurate receptor-mediated signaling and its regulation. Metabotropic glutamate receptor 5 (mGluR5) is a GPCR that plays a crucial role in circuit formation in the brain and also in various forms of synaptic plasticity including learning and memory. Outside the central nervous system this receptor also plays very important role in various other non-neuronal cells like heart cells, skin cells, hepatocytes, etc. Although the ligand-mediated endocytosis of mGluR5 has been studied in some detail, ligand-independent/constitutive endocytosis of the receptor has not been properly studied. Here, we have investigated the constitutive endocytosis of mGluR5 and also the sub-cellular fate of the receptor subsequent to internalization. We show here that mGluR5 undergoes constitutive internalization in HEK293 cells. Following endocytosis, the receptor enters the recycling compartment and no localization of the receptor was observed in the lysosome. In addition, we also report here that most of the receptors recycle to the cell surface subsequent to constitutive internalization. Thus, our data demonstrate that mGluR5 receptors internalize without the application of ligand and the internalized receptors recycle back to the cell surface following constitutive endocytosis.

摘要

配体依赖性和配体非依赖性的 G 蛋白偶联受体 (GPCR) 内吞转运对于准确的受体介导的信号转导及其调节至关重要。代谢型谷氨酸受体 5 (mGluR5) 是一种 GPCR,在大脑中的回路形成中发挥着关键作用,也在包括学习和记忆在内的各种形式的突触可塑性中发挥作用。在中枢神经系统之外,该受体在心脏细胞、皮肤细胞、肝细胞等各种其他非神经元细胞中也发挥着非常重要的作用。尽管已经对 mGluR5 的配体介导内吞作用进行了一些详细的研究,但对受体的配体非依赖性/组成型内吞作用还没有进行适当的研究。在这里,我们研究了 mGluR5 的组成型内吞作用以及内吞后受体的亚细胞命运。我们在这里表明,mGluR5 在 HEK293 细胞中发生组成型内吞作用。内吞作用后,受体进入再循环室,在溶酶体中未观察到受体定位。此外,我们还在这里报告说,大多数受体在组成型内吞作用后会重新循环到细胞表面。因此,我们的数据表明,mGluR5 受体在没有配体应用的情况下内化,并且内化的受体在组成型内吞作用后会重新循环到细胞表面。

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