胰岛素信号转导在2型糖尿病视网膜受损

Youde Jiang, Li Liu, Hainan Li, Jiemei Wang, J. Steinle
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引用次数: 5

摘要

2型糖尿病的发病率正在达到流行水平。然而,胰岛素抵抗引起的组织特异性改变直到最近才被研究。本研究的目的是评估2型糖尿病常见小鼠模型db/db小鼠的视网膜胰岛素信号转导。收集来自5个月大雄性db/db和db/+(对照)小鼠的视网膜裂解物,并对其进行蛋白质印迹或ELISA分析,以测定胰岛素受体、胰岛素受体底物-1(IRS-1)、Akt、肿瘤坏死因子α(TNFα)和胱天蛋白酶3水平。数据显示TNFα和IRS-1在丝氨酸307上的磷酸化增加。这导致丝氨酸473上的Akt磷酸化减少,并增加胱天蛋白酶3的切割。总之,这些数据表明db/db小鼠视网膜中的胰岛素信号功能失调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Insulin Signal Transduction is Impaired in the Type 2 Diabetic Retina
Rates of type 2 diabetes are reaching epidemic levels. Yet, the tissue specific alterations due to insulin resistance are only recently being investigated. The goal of the present study was to evaluate retinal insulin signal transduction in a common mouse model of type 2 diabetes, the db/db mouse. Retinal lysates from five month old male db/db and db/+ (control) mice were collected and processed for Western blotting or ELISA analyses for insulin receptor, insulin receptor substrate-1 (IRS-1), Akt, tumor necrosis factor alpha (TNFα) and caspase 3 levels. Data demonstrate increased TNFα and IRS-1 phosphorylation on serine 307. This led to decreased Akt phosphorylation on serine 473 and increased cleavage of caspase 3. Taken together, the data suggest dysfunctional insulin signaling in the retina of the db/db mouse.
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