Abousaab Abeer, Warsi Jamshed, Elvira Bernat, Lang Florian
Department of Physiology I, University of Tübingen, Gmelinstr. 5, 72076, Tübingen, Germany.
J Membr Biol. 2016 Jun;249(3):239-49. doi: 10.1007/s00232-015-9863-0. Epub 2015 Dec 21.
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.
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。