Department of Physiology, Saarland University, Building 59, 66421 Homburg, Germany.
Nat Commun. 2013;4:1439. doi: 10.1038/ncomms2467.
Cytotoxic T lymphocytes kill virus-infected and tumorigenic target cells through the release of perforin and granzymes via fusion of lytic granules at the contact site, the immunological synapse. It has been postulated that this fusion process is mediated by non-neuronal members of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor complex protein family. Here, using a synaptobrevin2-monomeric red fluorescence protein knock-in mouse we demonstrate that, surprisingly, the major neuronal v-SNARE synaptobrevin2 is expressed in cytotoxic T lymphocytes and exclusively localized on granzyme B-containing lytic granules. Cleavage of synaptobrevin2 by tetanus toxin or ablation of the synaptobrevin2 gene leads to a complete block of lytic granule exocytosis while leaving upstream events unaffected, identifying synaptobrevin2 as the v-SNARE responsible for the fusion of lytic granules at the immunological synapse.
细胞毒性 T 淋巴细胞通过在接触部位(免疫突触)融合裂解颗粒,释放穿孔素和颗粒酶来杀死病毒感染和致瘤靶细胞。据推测,这个融合过程是由可溶性 N-乙基马来酰亚胺敏感因子附着蛋白受体复合物蛋白家族的非神经元成员介导的。在这里,我们使用突触融合蛋白 2-单体红色荧光蛋白敲入小鼠证明,令人惊讶的是,主要的神经元 v-SNARE 突触融合蛋白 2在细胞毒性 T 淋巴细胞中表达,并且仅定位在含有颗粒酶 B 的裂解颗粒上。破伤风毒素切割突触融合蛋白 2或敲除突触融合蛋白 2 基因会导致裂解颗粒胞吐作用完全阻断,而不影响上游事件,从而确定突触融合蛋白 2是负责裂解颗粒在免疫突触融合的 v-SNARE。