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Characterization of purinergic receptor 2 signaling in podocytes from diabetic kidneys

机译:糖尿病肾的幽米细胞中嘌呤能受体2信号传导的特征

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摘要

Growing evidence suggests that renal purinergic signaling undergoes significant remodeling during pathophysiological conditions such as diabetes. This study examined the renal P2 receptor profile and ATP-mediated calcium response from podocytes in glomeruli from kidneys with type 1 or type 2 diabetic kidney disease (DKD), using type 2 diabetic nephropathy (T2DN) rats and streptozotocin-injected Dahl salt-sensitive (type 1 diabetes) rats. A dramatic increase in the ATP-mediated intracellular calcium flux in podocytes was observed in both models. Pharmacological inhibition established that P2X4 and P2X7 are the major receptors contributing to the augmented ATP-mediated intracellular calcium signaling in diabetic podocytes. The transition in purinergic receptor composition from metabotropic to ionotropic may disrupt intracellular calcium homeostasis in podocytes resulting in their dysfunction and potentially further aggravating DKD progression.
机译:日益增长的证据表明,肾嘌呤能信号传导在糖尿病等病理生理病症期间经历显着的重塑。本研究检测了肾P2受体型材和来自肾小球中的肾小球的肾细胞的ATP介导的钙反应来自肾脏的1型或2型糖尿病肾病(DKD),使用2型糖尿病肾病(T2DN)大鼠和链脲佐菌素注射的DAHL敏感性(1型糖尿病)大鼠。在两种模型中观察到幽平织物中ATP介导的细胞内钙通量的显着增加。药理抑制确定P2X4和P2X7是促进糖尿病哆粒细胞中增强ATP介导的细胞内钙信号传导的主要受体。从代谢到离子素的嘌呤能受体组合物中的过渡可能破坏细胞内钙稳态,导致它们的功能障碍,并且可能进一步加剧DKD进展。

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