K+-Cl- co-transporter 2 (KCC2) - a membrane trafficking perspective.

Q3 Biochemistry, Genetics and Molecular Biology
Molecular Membrane Biology Pub Date : 2016-09-01 Epub Date: 2017-11-16 DOI:10.1080/09687688.2017.1393566
Bor Luen Tang
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引用次数: 9

Abstract

K+-Cl- co-transporter 2 (KCC2/SLC12A5) is a neuronal specific cation chloride co-transporter which is active under isotonic conditions, and thus a key regulator of intracellular Cl- levels. It also has an ion transporter-independent structural role in modulating the maturation and regulation of excitatory glutamatergic synapses. KCC2 levels are developmentally regulated, and a postnatal upregulation of KCC2 generates a low intracellular chloride concentration that allows the neurotransmitters γ-aminobutyric acid (GABA) and glycine to exert inhibitory neurotransmission through its Cl- permeating channel. Functional expression of KCC2 at the neuronal cell surface is necessary for its activity, and impairment in KCC2 cell surface transport and/or internalization may underlie a range of neuropathological conditions. Although recent advances have shed light on a range of cellular mechanisms regulating KCC2 activity, little is known about its membrane trafficking itinerary and regulatory proteins. In this review, known membrane trafficking signals, pathways and mechanisms pertaining to KCC2's functional surface expression are discussed.

K+- cl -共转运蛋白2 (KCC2) -膜运输的视角。
K+-Cl-共转运蛋白2 (KCC2/SLC12A5)是一种神经元特异性阳离子氯共转运蛋白,在等渗条件下具有活性,因此是细胞内Cl-水平的关键调节因子。它在调节兴奋性谷氨酸突触的成熟和调节中也具有不依赖于离子转运蛋白的结构作用。KCC2水平在发育过程中受到调控,出生后KCC2的上调会产生较低的细胞内氯浓度,从而使神经递质γ-氨基丁酸(GABA)和甘氨酸通过其Cl-渗透通道抑制神经传递。KCC2在神经元细胞表面的功能性表达是其活性的必要条件,KCC2细胞表面运输和/或内化的损伤可能是一系列神经病理状况的基础。尽管最近的进展已经揭示了一系列调节KCC2活性的细胞机制,但对其膜运输路线和调节蛋白知之甚少。本文综述了已知的膜转运信号、与KCC2功能表面表达相关的途径和机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Membrane Biology
Molecular Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation. Molecular Membrane Biology provides a forum for high quality research that serves to advance knowledge in molecular aspects of biological membrane structure and function. The journal welcomes submissions of original research papers and reviews in the following areas: • Membrane receptors and signalling • Membrane transporters, pores and channels • Synthesis and structure of membrane proteins • Membrane translocation and targeting • Lipid organisation and asymmetry • Model membranes • Membrane trafficking • Cytoskeletal and extracellular membrane interactions • Cell adhesion and intercellular interactions • Molecular dynamics and molecular modelling of membranes. • Antimicrobial peptides.
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