Leek Ashley N, Quinn Josiah A, Krapf Diego, Tamkun Michael M
Department of Biomedical Sciences, Colorado State University, Fort Collins, CO, United States.
Molecular, Cellular and Integrative Neuroscience Program, Colorado State University, Fort Collins, CO, United States.
Front Cell Dev Biol. 2024 Feb 1;12:1334861. doi: 10.3389/fcell.2024.1334861. eCollection 2024.
Astrocytic GLT-1 glutamate transporters ensure the fidelity of glutamic neurotransmission by spatially and temporally limiting glutamate signals. The ability to limit neuronal hyperactivity relies on the localization and diffusion of GLT-1 on the astrocytic surface, however, little is known about the underlying mechanisms. We show that two isoforms of GLT-1, GLT-1a and GLT-1b, form nanoclusters on the surface of transfected astrocytes and HEK-293 cells. We used both fixed and live cell super-resolution imaging of fluorescent protein and epitope tagged proteins in co-cultures of rat astrocytes and neurons. Immunofluorescence techniques were also used. GLT1 diffusion was assessed via single particle tracking and fluorescence recovery after photobleach (FRAP). We found GLT-1a, but not GLT-1b, nanoclusters concentrated adjacent to actin filaments which was maintained after addition of glutamate. GLT-1a nanocluster concentration near actin filaments was prevented by expression of a cytosolic GLT-1a C-terminus, suggesting the C-terminus is involved in the localization adjacent to cortical actin. Using super-resolution imaging, we show that astrocytic GLT-1a and actin co-localize in net-like structures around neuronal Kv2.1 clusters at points of neuron/astrocyte contact. Overall, these data describe a novel relationship between GLT-1a and cortical actin filaments, which localizes GLT-1a near neuronal structures responsive to ischemic insult.
星形胶质细胞的谷氨酸转运体-1(GLT-1)通过在空间和时间上限制谷氨酸信号来确保谷氨酸神经传递的保真度。限制神经元过度活跃的能力依赖于GLT-1在星形胶质细胞表面的定位和扩散,然而,其潜在机制尚不清楚。我们发现,GLT-1的两种亚型GLT-1a和GLT-1b在转染的星形胶质细胞和人胚肾293(HEK-293)细胞表面形成纳米簇。我们在大鼠星形胶质细胞和神经元的共培养物中,对荧光蛋白和表位标记蛋白进行了固定细胞和活细胞超分辨率成像。还使用了免疫荧光技术。通过单粒子追踪和光漂白后荧光恢复(FRAP)评估GLT-1的扩散。我们发现,GLT-1a而非GLT-1b纳米簇集中在肌动蛋白丝附近,添加谷氨酸后仍保持这种状态。胞质GLT-1a C末端的表达可阻止GLT-1a纳米簇在肌动蛋白丝附近的聚集,这表明C末端参与了与皮质肌动蛋白相邻的定位。通过超分辨率成像,我们发现星形胶质细胞的GLT-1a和肌动蛋白在神经元/星形胶质细胞接触点处围绕神经元Kv2.1簇的网状结构中共定位。总体而言,这些数据描述了GLT-1a与皮质肌动蛋白丝之间的新关系,这种关系将GLT-1a定位在对缺血性损伤有反应的神经元结构附近。