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神经营养因子-3通过Akt信号通路减少6-羟基多巴胺诱导的PC12细胞凋亡。

Neurotrophin-3 reduces apoptosis induced by 6-OHDA in PC12 cells through Akt signaling pathway.

作者信息

Li Zhiquan, Hu Yunyu, Zhu Qingsheng, Zhu Jinyu

机构信息

PLA Institute of Othropadics & Traumatology, Xijing Hospital, The Fourth Military Medical University, Xi'an 710032, China.

出版信息

Int J Dev Neurosci. 2008 Oct;26(6):635-40. doi: 10.1016/j.ijdevneu.2008.03.009. Epub 2008 Apr 4.

Abstract

Previous work has demonstrated that 6-hydroxydopamine (6-OHDA) induces apoptosis in PC12 cells. The goal of the present study was to investigate the mechanisms underlying the protection by neurotrophin-3 (NT-3) against 6-OHDA-induced apoptosis in PC12 cells. Treatment of PC12 cells with 6-OHDA resulted in activation of caspase-3 and subsequent apoptosis, as detected by TUNEL staining. In addition, Akt phosphorylation was decreased following 6-OHDA treatment. Pretreatment with NT-3 reduced the percentage of apoptotic cells and caspase-3 activity induced by 6-OHDA and suppressed the cleavage of caspase-3 and Poly(ADP-ribose) polymerase (PARP) with a significant decrease in cell viability. Moreover, Akt phosphorylation was enhanced and 6-OHDA-induced chromatin condensation was suppressed by NT-3. Such NT-3-evoked suppression in chromatin condensation was reversed by anti-TrkA antibody receptor blockade. Further study revealed that LY294002, an inhibitor of PI3-kinase (a molecule upstream of Akt), enhanced 6-OHDA-induced apoptosis. These data indicate that NT-3 prevents 6-OHDA-induced apoptosis in PC12 cells via activation of PI3-kinase/Akt pathway.

摘要

先前的研究表明,6-羟基多巴胺(6-OHDA)可诱导PC12细胞凋亡。本研究的目的是探讨神经营养因子-3(NT-3)对6-OHDA诱导的PC12细胞凋亡的保护机制。用6-OHDA处理PC12细胞导致半胱天冬酶-3激活及随后的凋亡,这通过TUNEL染色检测到。此外,6-OHDA处理后Akt磷酸化水平降低。用NT-3预处理可降低6-OHDA诱导的凋亡细胞百分比和半胱天冬酶-3活性,并抑制半胱天冬酶-3和聚(ADP-核糖)聚合酶(PARP)的裂解,细胞活力显著下降。此外,NT-3增强了Akt磷酸化,并抑制了6-OHDA诱导的染色质凝聚。抗TrkA抗体受体阻断可逆转NT-3引起的染色质凝聚抑制。进一步研究表明,PI3激酶(Akt上游分子)抑制剂LY294002增强了6-OHDA诱导的细胞凋亡。这些数据表明,NT-3通过激活PI3激酶/Akt途径预防6-OHDA诱导的PC12细胞凋亡。

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