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促氧化剂衔接蛋白p66SHC对选择性B细胞自噬的调控

Regulation of Selective B Cell Autophagy by the Pro-oxidant Adaptor p66SHC.

作者信息

Onnis Anna, Cassioli Chiara, Finetti Francesca, Baldari Cosima T

机构信息

Department of Life Sciences, University of Siena, Siena, Italy.

出版信息

Front Cell Dev Biol. 2020 Mar 26;8:193. doi: 10.3389/fcell.2020.00193. eCollection 2020.

Abstract

p66SHC is a pro-oxidant member of the SHC family of protein adaptors that acts as a negative regulator of cell survival. In lymphocytes p66SHC exploits both its adaptor and its reactive oxygen species (ROS)-elevating function to antagonize mitogenic and survival signaling and promote apoptosis. As a result, p66SHC deficiency leads to the abnormal expansion of peripheral T and B cells and lupus-like autoimmunity. Additionally, a defect in p66SHC expression is a hallmark of B cell chronic lymphocytic leukemia, where it contributes to the accumulation of long-lived neoplastic cells. We have recently provided evidence that p66SHC exerts a further layer of control on B cell homeostasis by acting as a new mitochondrial LC3-II receptor to promote the autophagic demise of dysfunctional mitochondria. Here we discuss this finding in the context of the autophagic control of B cell homeostasis, development, and differentiation in health and disease.

摘要

p66SHC是蛋白质衔接子SHC家族的一种促氧化剂成员,作为细胞存活的负调节因子发挥作用。在淋巴细胞中,p66SHC利用其衔接子功能和提高活性氧(ROS)的功能来拮抗有丝分裂和存活信号并促进细胞凋亡。因此,p66SHC缺陷会导致外周T细胞和B细胞异常扩增以及狼疮样自身免疫。此外,p66SHC表达缺陷是B细胞慢性淋巴细胞白血病的一个标志,它促使长寿肿瘤细胞积累。我们最近提供的证据表明,p66SHC作为一种新的线粒体LC3-II受体,通过促进功能失调线粒体的自噬性死亡,对B细胞内稳态施加了另一层控制。在此,我们在健康和疾病状态下B细胞内稳态、发育和分化的自噬控制背景下讨论这一发现。

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