Stinchcombe Jane C, Majorovits Endre, Bossi Giovanna, Fuller Stephen, Griffiths Gillian M
Sir William Dunn School of Pathology, South Parks Road, Oxford OX1 3RE, UK.
Nature. 2006 Sep 28;443(7110):462-5. doi: 10.1038/nature05071.
Cytotoxic T lymphocytes (CTLs) destroy virally infected and tumorigenic cells by releasing the contents of specialized secretory lysosomes--termed 'lytic granules'--at the immunological synapse formed between the CTL and the target. On contact with the target cell, the microtubule organizing centre of the CTL polarizes towards the target and granules move along microtubules in a minus-end direction towards the polarized microtubule organizing centre. However, the final steps of secretion have remained unclear. Here we show that CTLs do not require actin or plus-end microtubule motors for secretion, but instead the centrosome moves to and contacts the plasma membrane at the central supramolecular activation cluster of the immunological synapse. Actin and IQGAP1 are cleared away from the synapse, and granules are delivered directly to the plasma membrane. These data show that CTLs use a previously unreported mechanism for delivering secretory granules to the immunological synapse, with granule secretion controlled by centrosome delivery to the plasma membrane.
细胞毒性T淋巴细胞(CTL)通过在CTL与靶细胞之间形成的免疫突触处释放特殊分泌性溶酶体(称为“裂解颗粒”)的内容物,来破坏病毒感染细胞和致瘤细胞。与靶细胞接触时,CTL的微管组织中心向靶细胞极化,颗粒沿着微管向负极方向移动,朝向极化的微管组织中心。然而,分泌的最终步骤仍不清楚。在这里,我们表明CTL分泌不需要肌动蛋白或微管正极马达,而是中心体移动到免疫突触的中央超分子激活簇并与质膜接触。肌动蛋白和IQGAP1从突触处清除,颗粒直接递送至质膜。这些数据表明,CTL使用一种以前未报道的机制将分泌颗粒递送至免疫突触,颗粒分泌由中心体向质膜的递送控制。