Departments of Biochemistry.
Physiology, Universidad Central del Caribe, Bayamón.
Neuroreport. 2020 Apr 8;31(6):450-455. doi: 10.1097/WNR.0000000000001427.
Protecting neurons from neurotoxicity is a job mainly performed by astrocytes through glutamate uptake and potassium buffering. These functions are aided principally by the Kir4.1 inwardly rectifying potassium channels located in the membrane of astrocytes. Astrocytes grown in hyperglycemic conditions have decreased levels of Kir4.1 potassium channels as well as impaired potassium and glutamate uptake. Previous studies performed in a human corneal epithelial cell injury model demonstrated a mechanism of regulation of Kir4.1 expression via the binding of microRNA-250 (miR-205) to the Kir4.1 3´ untranslated region. Our purpose is to test if astrocytes express miR-205 and elucidate its role in regulating Kir4.1 expression in astrocytes grown in hyperglycemic conditions. We used quantitative-PCR to assess the levels of miR-205 in astrocytes grown in high glucose (25 mM) medium compared to astrocytes grown in normal glucose (5 mM). We found that not only was miR-205 expressed in astrocytes grown in normal glucose, but its expression was increased up to six-fold in astrocytes grown in hyperglycemic conditions. Transfection of miR-205 mimic or inhibitor was performed to alter the levels of miR-205 in astrocytes followed by western blot to assess Kir4.1 channel levels in these cells. Astrocytes treated with miR-205 mimic had a 38.6% reduction of Kir4.1 protein levels compared to control (mock-transfected) cells. In contrast, astrocytes transfected with miR-205 inhibitor were significantly upregulated compared to mock by 47.4%. Taken together, our data indicate that miR-205 negatively regulates the expression of Kir4.1 in astrocytes grown in hyperglycemic conditions.
保护神经元免受神经毒性的侵害主要是由星形胶质细胞通过摄取谷氨酸和缓冲钾来完成的。这些功能主要由位于星形胶质细胞膜上的 Kir4.1 内向整流钾通道辅助。在高血糖条件下生长的星形胶质细胞 Kir4.1 钾通道水平降低,以及钾和谷氨酸摄取受损。以前在人角膜上皮细胞损伤模型中进行的研究表明,通过 microRNA-250 (miR-205) 与 Kir4.1 3'非翻译区的结合,调节 Kir4.1 表达的机制。我们的目的是测试星形胶质细胞是否表达 miR-205,并阐明其在调节高血糖条件下星形胶质细胞中 Kir4.1 表达中的作用。我们使用定量 PCR 来评估在高葡萄糖(25mM)培养基中生长的星形胶质细胞与在正常葡萄糖(5mM)中生长的星形胶质细胞相比,miR-205 的水平。我们发现,不仅在正常葡萄糖中生长的星形胶质细胞中表达了 miR-205,而且在高血糖条件下生长的星形胶质细胞中表达增加了六倍。转染 miR-205 模拟物或抑制剂来改变星形胶质细胞中 miR-205 的水平,然后通过 Western blot 来评估这些细胞中 Kir4.1 通道的水平。与对照(模拟转染)细胞相比,用 miR-205 模拟物处理的星形胶质细胞的 Kir4.1 蛋白水平降低了 38.6%。相比之下,用 miR-205 抑制剂转染的星形胶质细胞与对照相比显著上调了 47.4%。总之,我们的数据表明,miR-205 负调控高血糖条件下星形胶质细胞中 Kir4.1 的表达。