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Requirement for AHNAK1-mediated calcium signaling during T lymphocyte cytolysis

机译:T淋巴细胞细胞溶解过程中对AHNAK1介导的钙信号的要求

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摘要

Cytolytic CD8+ T cells (CTLs) kill virally infected cells, tumor cells, or other potentially autoreactive T cells in a calcium-dependent manner. To date, the molecular mechanism that leads to calcium intake during CTL differentiation and function has remained unresolved. We demonstrate that desmoyokin (AHNAK1) is expressed in mature CTLs, but not in naive CD8+ T cells, and is critical for calcium entry required for their proper function during immune response. We show that mature AHNAK1-deficient CTLs exhibit reduced Cav1.1 α1 subunit expression (also referred to as L-type calcium channels or α1S pore-forming subunits), which recently were suggested to play a role in calcium entry into CD4+ T cells. AHNAK1-deficient CTLs show marked reduction in granzyme-B production, cytolytic activity, and IFN-γ secretion after T cell receptor stimulation. Our results demonstrate an AHNAK1-dependent mechanism controlling calcium entry during CTL effector function.
机译:细胞溶解性CD8 + T细胞(CTL)以钙依赖的方式杀死病毒感染的细胞,肿瘤细胞或其他潜在的自身反应性T细胞。迄今为止,在CTL分化和功能过程中导致钙摄入的分子机制尚未解决。我们证明,desmoyokin(AHNAK1)在成熟的CTL中表达,但在幼稚的CD8 + T细胞中不表达,并且对于钙在其免疫应答过程中的正常功能所需的钙进入至关重要。我们表明,成熟的AHNAK1缺陷型CTL表现出降低的Cav1.1α1亚基表达(也称为L型钙通道或α1S孔形成亚基),最近被认为在钙进入CD4 + T细胞中发挥作用。 AHNAK1缺陷型CTL在T细胞受体刺激后,颗粒酶B的产生,细胞溶解活性和IFN-γ分泌显着降低。我们的研究结果证明了AHNAK1依赖性机制可控制CTL效应子功能期间的钙进入。

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