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兴奋性氨基酸转运体EAAT1、EAAT2、EAAT3和EAAT4对小窝蛋白-1的敏感性

Caveolin-1 Sensitivity of Excitatory Amino Acid Transporters EAAT1, EAAT2, EAAT3, and EAAT4.

作者信息

Abousaab Abeer, Warsi Jamshed, Elvira Bernat, Lang Florian

机构信息

Department of Physiology I, University of Tübingen, Gmelinstr. 5, 72076, Tübingen, Germany.

出版信息

J Membr Biol. 2016 Jun;249(3):239-49. doi: 10.1007/s00232-015-9863-0. Epub 2015 Dec 21.

Abstract

Excitatory amino acid transporters EAAT1 (SLC1A3), EAAT2 (SLC1A2), EAAT3 (SLC1A1), and EAAT4 (SLC1A6) serve to clear L-glutamate from the synaptic cleft and are thus important for the limitation of neuronal excitation. EAAT3 has previously been shown to form complexes with caveolin-1, a major component of caveolae, which participate in the regulation of transport proteins. The present study explored the impact of caveolin-1 on electrogenic transport by excitatory amino acid transporter isoforms EAAT1-4. To this end cRNA encoding EAAT1, EAAT2, EAAT3, or EAAT4 was injected into Xenopus oocytes without or with additional injection of cRNA encoding caveolin-1. The L-glutamate (2 mM)-induced inward current (I Glu) was taken as a measure of glutamate transport. As a result, I Glu was observed in EAAT1-, EAAT2-, EAAT3-, or EAAT4-expressing oocytes but not in water-injected oocytes, and was significantly decreased by coexpression of caveolin-1. Caveolin-1 decreased significantly the maximal transport rate. Treatment of EAATs-expressing oocytes with brefeldin A (5 µM) was followed by a decrease in conductance, which was similar in oocytes expressing EAAT together with caveolin-1 as in oocytes expressing EAAT1-4 alone. Thus, caveolin-1 apparently does not accelerate transporter protein retrieval from the cell membrane. In conclusion, caveolin-1 is a powerful negative regulator of the excitatory glutamate transporters EAAT1, EAAT2, EAAT3, and EAAT4.

摘要

兴奋性氨基酸转运体EAAT1(SLC1A3)、EAAT2(SLC1A2)、EAAT3(SLC1A1)和EAAT4(SLC1A6)负责清除突触间隙中的L - 谷氨酸,因此对于限制神经元兴奋很重要。此前已表明EAAT3可与小窝蛋白 - 1(小窝的主要成分)形成复合物,小窝蛋白 - 1参与转运蛋白的调节。本研究探讨了小窝蛋白 - 1对兴奋性氨基酸转运体亚型EAAT1 - 4的电转运的影响。为此,将编码EAAT1、EAAT2、EAAT3或EAAT4的cRNA注射到非洲爪蟾卵母细胞中,有无额外注射编码小窝蛋白 - 1的cRNA。以L - 谷氨酸(2 mM)诱导的内向电流(I Glu)作为谷氨酸转运的指标。结果,在表达EAAT1、EAAT2、EAAT3或EAAT4的卵母细胞中观察到I Glu,但在注射水的卵母细胞中未观察到,并且小窝蛋白 - 1的共表达显著降低了I Glu。小窝蛋白 - 1显著降低了最大转运速率。用布雷菲德菌素A(5 μM)处理表达EAATs的卵母细胞后,其电导降低,在与小窝蛋白 - 1一起表达EAAT的卵母细胞中与单独表达EAAT1 - 4的卵母细胞中相似。因此,小窝蛋白 - 1显然不会加速转运蛋白从细胞膜的回收。总之,小窝蛋白 - 1是兴奋性谷氨酸转运体EAAT1、EAAT2、EAAT3和EAAT4的强大负调节因子。

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