Smyd1C Mediates CD8 T Cell Death via Regulation of Bcl2-Mediated Restriction of outer Mitochondrial Membrane Integrity.

Journal of Cell Signaling Pub Date : 2017-09-01 Epub Date: 2017-09-12 DOI:10.4172/2576-1471.1000163
Hui Nie, Gary Rathbun, Haley Tucker
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引用次数: 6

Abstract

The SET and Mynd domain 1 (Smyd1) locus encodes three tissue-restricted isoforms. Two previously characterized isoforms, Smyd1A and Smyd1B, are heart and skeletal muscle-restricted histone methyl transferases. Here we report that a third, non-catalytic isoform, Smyd1C, is expressed predominantly in activated CD8 T cells. While Smyd1C- deficient CD8 T cells undergo activation-induced apoptosis, neither of two classical mechanisms activation-induced cell death nor activated cell autonomous death are utilized. Instead, Smyd1C accumulates within both mitochondria and the immunological synapse where it associates with Bcl-2, FK506-Binding Protein 8/38 (FKBP38) and Calcineurin. This complex maintains Bcl-2 phosphorylation, enhanced mitochondrial localization, and restricted apoptosis of activated CD8 T cells. We suggest that CD8 T cell death is governed, in part, by Smyd1C regulation of Bcl2-mediated restriction of outer mitochondrial membrane integrity.

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Smyd1C通过调控bcl2介导的线粒体外膜完整性限制介导CD8 T细胞死亡。
SET和Mynd结构域1 (Smyd1)位点编码三种组织限制性亚型。两个先前表征的亚型,Smyd1A和Smyd1B,是心脏和骨骼肌限制性组蛋白甲基转移酶。在这里,我们报告了第三种非催化异构体Smyd1C主要在活化的CD8 T细胞中表达。当Smyd1C缺陷的CD8 T细胞经历激活诱导的凋亡时,激活诱导的细胞死亡和激活的细胞自主死亡两种经典机制都没有被利用。相反,Smyd1C在线粒体和免疫突触中积累,在那里它与Bcl-2、fk506结合蛋白8/38 (FKBP38)和钙调磷酸酶相关。该复合物维持Bcl-2磷酸化,增强线粒体定位,并限制活化CD8 T细胞的凋亡。我们认为CD8 T细胞死亡在一定程度上受Smyd1C调节bcl2介导的线粒体外膜完整性限制所控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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