Nishii Naoko, Kawai Tomoko, Yasuoka Hiroki, Abe Tadashi, Tatsumi Nanami, Harada Yuika, Miyaji Takaaki, Li Shunai, Tsukano Moemi, Watanabe Masami, Ogawa Daisuke, Wada Jun, Takei Kohji, Yamada Hiroshi
Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Okayama 700-8558, Japan.
Department of Cell Physiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Okayama 700-8558, Japan.
Int J Mol Sci. 2025 Mar 11;26(6):2485. doi: 10.3390/ijms26062485.
Glomerular podocytes act as a part of the filtration barrier in the kidney. The activity of this filter is regulated by ionotropic and metabotropic glutamate receptors. Adjacent podocytes can potentially release glutamate into the intercellular space; however, little is known about how podocytes release glutamate. Here, we demonstrated vesicular glutamate transporter 3 (VGLUT3)-dependent glutamate release from podocytes. Immunofluorescence analysis revealed that rat glomerular podocytes and an immortal mouse podocyte cell line (MPC) express VGLUT1 and VGLUT3. Consistent with this finding, quantitative RT-PCR revealed the expression of VGLUT1 and VGLUT3 mRNA in undifferentiated and differentiated MPCs. In addition, the exocytotic proteins vesicle-associated membrane protein 2, synapsin 1, and synaptophysin 1 were present in punctate patterns and colocalized with VGLUT3 in MPCs. Interestingly, approximately 30% of VGLUT3 colocalized with VGLUT1. By immunoelectron microscopy, VGLUT3 was often observed around clear vesicle-like structures in differentiated MPCs. Differentiated MPCs released glutamate following depolarization with high potassium levels and after stimulation with the muscarinic agonist pilocarpine. The depletion of VGLUT3 in MPCs by RNA interference reduced depolarization-dependent glutamate release. These results strongly suggest that VGLUT3 is involved in glutamatergic signalling in podocytes and may be a new drug target for various kidney diseases.
肾小球足细胞是肾脏滤过屏障的一部分。该滤过器的活性受离子型和代谢型谷氨酸受体调节。相邻的足细胞可能会将谷氨酸释放到细胞间空间;然而,关于足细胞如何释放谷氨酸知之甚少。在这里,我们证明了足细胞通过囊泡谷氨酸转运体3(VGLUT3)释放谷氨酸。免疫荧光分析显示,大鼠肾小球足细胞和永生小鼠足细胞系(MPC)表达VGLUT1和VGLUT3。与此发现一致,定量逆转录聚合酶链反应显示未分化和分化的MPC中VGLUT1和VGLUT3 mRNA的表达。此外,胞吐蛋白囊泡相关膜蛋白2、突触素1和突触囊泡蛋白1呈点状分布,并与MPC中的VGLUT3共定位。有趣的是,约30%的VGLUT3与VGLUT1共定位。通过免疫电子显微镜观察,在分化的MPC中,VGLUT3常出现在透明囊泡样结构周围。分化的MPC在高钾水平去极化后以及用毒蕈碱激动剂毛果芸香碱刺激后释放谷氨酸。RNA干扰使MPC中的VGLUT3耗竭,减少了去极化依赖性谷氨酸释放。这些结果强烈表明,VGLUT3参与足细胞中的谷氨酸能信号传导,可能是各种肾脏疾病的新药物靶点。