The Ca Signalling Group, Department of Biochemistry and Molecular Cell Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Institute for Neuroimmunology and Multiple Sclerosis Research, University Medical Centre Göttingen, 37075 Göttingen, Germany.
Sci Signal. 2021 Mar 23;14(675):eabd5647. doi: 10.1126/scisignal.abd5647.
NAADP-evoked Ca release through type 1 ryanodine receptors (RYR1) is a major mechanism underlying the earliest signals in T cell activation, which are the formation of Ca microdomains. In our characterization of the molecular machinery underlying NAADP action, we identified an NAADP-binding protein, called hematological and neurological expressed 1-like protein (HN1L) [also known as Jupiter microtubule-associated homolog 2 (JPT2)]. Gene deletion of in human Jurkat and primary rat T cells resulted in decreased numbers of initial Ca microdomains and delayed the onset and decreased the amplitude of global Ca signaling. Photoaffinity labeling demonstrated direct binding of NAADP to recombinant HN1L/JPT2. T cell receptor/CD3-dependent coprecipitation of HN1L/JPT2 with RYRs and colocalization of these proteins suggest that HN1L/JPT2 connects NAADP formation with the activation of RYR channels within the first seconds of T cell activation. Thus, HN1L/JPT2 enables NAADP to activate Ca release from the endoplasmic reticulum through RYR.
NAADP 引发的通过类型 1 ryanodine 受体 (RYR1) 的 Ca2+释放是 T 细胞激活的最早信号的主要机制,其是 Ca2+微区的形成。在我们对 NAADP 作用的分子机制的表征中,我们鉴定了一种 NAADP 结合蛋白,称为血液和神经表达 1 样蛋白 (HN1L) [也称为木星微管相关同源物 2 (JPT2)]。在人 Jurkat 和原代大鼠 T 细胞中敲除 基因导致初始 Ca2+微区数量减少,并且延迟了全局 Ca2+信号的起始和幅度降低。光亲和标记证明了 NAADP 与重组 HN1L/JPT2 的直接结合。T 细胞受体/CD3 依赖性共沉淀表明 HN1L/JPT2 与 RYRs 共沉淀,并且这些蛋白质的共定位表明 HN1L/JPT2 将 NAADP 的形成与 T 细胞激活最初几秒钟内 RYR 通道的激活联系起来。因此,HN1L/JPT2 使 NAADP 能够通过 RYR 从内质网中激活 Ca2+释放。