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Localization of heat shock proteins in cerebral cortical cultures following induction by celastrol

机译:Celastrol诱导后大脑皮层培养物中热激蛋白的定位

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Hsp70, Hsp32, and Hsp27 were induced by celastrol in rat cerebral cortical cultures at dosages that did not affect cell viability. Pronounced differences were observed in the cellular localization of these heat shock proteins in cell types of cerebral cortical cultures. Celastrol-induced Hsp70 localized to the cell body and cellular processes of neurons that were identified by neuron-specific βIII-tubulin. Hsp70 was not detected in adjacent GFAP-positive glial cells that demonstrated a strong signal for Hsp27 and Hsp32 in both glial cell bodies and cellular processes. Cells in the cerebral cortex region of the brain are selectively impacted during the progression of Alzheimer’s disease which is a “protein misfolding disorder.” Heat shock proteins provide a line of defense against misfolded, aggregation-prone proteins. Celastrol is a potential agent to counter this neurodegenerative disorder as recent evidence indicates that in vivo administration of celastrol in a transgenic model of Alzheimer’s reduces an important neuropathological hallmark of this disease, namely, amyloid beta pathology that involves protein aggregation.
机译:Hsp70,Hsp32和Hsp27是由Celastrol在不影响细胞生存力的剂量下在大鼠大脑皮层培养物中诱导的。在大脑皮层培养物的细胞类型中,这些热激蛋白的细胞定位中观察到明显差异。 Celastrol诱导的Hsp70定位于通过神经元特异性βIII-微管蛋白鉴定的神经元的细胞体和细胞过程。在相邻的GFAP阳性神经胶质细胞中未检测到Hsp70,该神经胶质细胞在神经胶质细胞体和细胞过程中均表现出Hsp27和Hsp32的强信号。在阿尔茨海默氏病(一种称为“蛋白质错误折叠障碍”)的进展过程中,选择性地影响了大脑大脑皮质区域的细胞。热激蛋白提供了针对错误折叠,易于聚集的蛋白的防御线。 Celastrol是对抗这种神经退行性疾病的潜在药物,因为最近的证据表明,在阿尔茨海默氏病转基因模型中体内施用Celastrol可以降低该疾病的重要神经病理学特征,即涉及蛋白质聚集的β淀粉样蛋白病理。

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