iNOVA4Health, CEDOC, NOVA Medical School, NMS, Universidade NOVA de Lisboa, 1169-056 Lisboa, Portugal.
J Cell Sci. 2021 Jun 1;134(11). doi: 10.1242/jcs.246694. Epub 2021 Jun 8.
Lysosomes are dynamic organelles, capable of undergoing exocytosis. This process is crucial for several cellular functions, namely plasma membrane repair. Nevertheless, the molecular machinery involved in this process is poorly understood. Here, we identify Rab11a and Rab11b as regulators of Ca2+-induced lysosome exocytosis. Interestingly, Rab11-positive vesicles transiently interact with lysosomes at the cell periphery, indicating that this interaction is required for the last steps of lysosome exocytosis. Additionally, we found that the silencing of the exocyst subunit Sec15, a Rab11 effector, impairs lysosome exocytosis, suggesting that Sec15 acts together with Rab11 in the regulation of lysosome exocytosis. Furthermore, we show that Rab11 binds the guanine nucleotide exchange factor for Rab3a (GRAB) as well as Rab3a, which we have previously described to be a regulator of the positioning and exocytosis of lysosomes. Thus, our study identifies new players required for lysosome exocytosis and suggest the existence of a Rab11-Rab3a cascade involved in this process.
溶酶体是具有动态性的细胞器,能够发生胞吐作用。这一过程对于几种细胞功能至关重要,即质膜修复。然而,这一过程所涉及的分子机制尚不清楚。在这里,我们鉴定出 Rab11a 和 Rab11b 是 Ca2+诱导的溶酶体胞吐作用的调节因子。有趣的是,Rab11 阳性囊泡在细胞边缘与溶酶体短暂相互作用,表明这种相互作用是溶酶体胞吐作用的最后步骤所必需的。此外,我们发现外被体亚基 Sec15(Rab11 的效应因子)的沉默会损害溶酶体胞吐作用,表明 Sec15 与 Rab11 一起在溶酶体胞吐作用的调节中发挥作用。此外,我们还表明 Rab11 与我们之前描述的调节溶酶体定位和胞吐作用的 Rab3a 的鸟嘌呤核苷酸交换因子(GRAB)以及 Rab3a 结合。因此,我们的研究确定了溶酶体胞吐作用所需的新参与者,并提出了一个参与该过程的 Rab11-Rab3a 级联反应。