Mishra Kanchan Kumar, Gupta Sakshi, Banerjee Kakoli
Eukaryotic Gene Expression Lab National Institute of Immunology, New Delhi, India.
IUBMB Life. 2016 Jun;68(6):468-76. doi: 10.1002/iub.1505. Epub 2016 Apr 26.
Cytokines and growth factors play an important role in neuronal survival as well as cell death. The family of suppressors of cytokine signalling (SOCS) proteins, which includes SOCS1-7 and cytokine-induced suppressor (CIS), has been shown to act as negative regulators of cytokine-induced signalling. In this report, we highlight the role of SOCS3 in regulating neuronal differentiation and survival. We observed increased SOCS3 expression upon differentiation of PC12 cells as well as neural stem cells. SOCS3 overexpression upregulated differentiation of both neural stem cells and PC12 cells even in the absence of NGF, as evidenced by enhanced neurite outgrowth and upregulation of GAP43, marker associated with neurite outgrowth. siRNA-mediated silencing of SOCS3 confirmed the potential role of SOCS3 in neuritogenesis. We observed that, SOCS3-induced neurite differentiation was mediated via the PI3 kinase pathway. Another interesting observation was that SOCS3 overexpression promoted neuronal cell survival under H2 O2 -mediated stress indicating its fundamental role in cell survival. In conclusion, our results indicate that SOCS3 promotes differentiation and survival of neural cells and could be potentially useful in future therapy for treatment of neurodegenerative disorders. © 2016 IUBMB Life, 68(6):468-476, 2016.
细胞因子和生长因子在神经元存活以及细胞死亡过程中发挥着重要作用。细胞因子信号转导抑制因子(SOCS)蛋白家族,包括SOCS1 - 7和细胞因子诱导的抑制因子(CIS),已被证明可作为细胞因子诱导信号的负调节因子。在本报告中,我们着重阐述了SOCS3在调节神经元分化和存活中的作用。我们观察到,PC12细胞以及神经干细胞分化时SOCS3表达增加。即使在没有神经生长因子(NGF)的情况下,SOCS3的过表达也会上调神经干细胞和PC12细胞的分化,这通过神经突生长增强以及与神经突生长相关的标志物GAP43的上调得以证明。siRNA介导的SOCS3沉默证实了SOCS3在神经突发生中的潜在作用。我们观察到,SOCS3诱导的神经突分化是通过PI3激酶途径介导的。另一个有趣的发现是,SOCS3过表达在H2O2介导的应激下促进神经元细胞存活,表明其在细胞存活中的重要作用。总之,我们的结果表明,SOCS3促进神经细胞的分化和存活,可能在未来神经退行性疾病的治疗中具有潜在用途。© 2016国际生物化学与分子生物学联盟生命科学,68(6):468 - 476,2016。