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Epidermal Growth Factor Receptor Activation: An Upstream Signal for Transition of Quiescent Astrocytes into Reactive Astrocytes after Neural Injury

机译:表皮生长因子受体激活:神经损伤后静态星形胶质细胞转变为反应性星形胶质细胞的上游信号。

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摘要

Modulating the behaviors of reactive astrocytes is a potential therapeutic strategy for neurodegenerative diseases. We found that upregulation and activation of the epidermal growth factor receptor (EGFR) occur in astrocytes after different injuries in optic nerves in vivo. Activation of EGFR regulates genes and cellular processes representing most major markers of reactive astrocytes and genes related with glaucomatous optic neuropathy and other neural disorders. These results suggest that activation of EGFR is a common, regulatory pathway that triggers quiescent astrocytes into reactive astrocytes in response to neural injuries in the optic nerve, and perhaps other parts of the CNS. Targeting EGFR activation using an EGFR tyrosine kinase inhibitor prevents the loss of retinal ganglion cells in a model of glaucomatous optic neuropathy. Because these inhibitors are currently used clinically, our results present an approach to reactive astrocytes as a potential new target for the treatment of neurodegenerations.
机译:调节反应性星形胶质细胞的行为是神经退行性疾病的潜在治疗策略。我们发现表皮生长因子受体(EGFR)的上调和激活发生在体内视神经不同损伤后的星形胶质细胞中。 EGFR的激活调节代表星形胶质细胞反应性星形胶质细胞和与青光眼性视神经病变及其他神经疾病有关的基因的大多数主要标志物的基因和细胞过程。这些结果表明,EGFR的激活是一种常见的调节性途径,可对视神经以及中枢神经系统其他部位的神经损伤做出反应,从而将静止的星形胶质细胞转化为活性星形胶质细胞。使用EGFR酪氨酸激酶抑制剂靶向EGFR激活可防止青光眼视神经病变模型中视网膜神经节细胞的丢失。因为这些抑制剂目前在临床上使用,所以我们的结果提出了一种反应性星形胶质细胞的方法,作为治疗神经变性的潜在新靶标。

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