Department of Molecular Neurogenetics, European Neuroscience Institute, 37077 Göttingen, Germany.
Proc Natl Acad Sci U S A. 2012 Nov 13;109(46):18944-9. doi: 10.1073/pnas.1203306109. Epub 2012 Oct 25.
Neurons secrete neuropeptides from dense core vesicles (DCVs) to modulate neuronal activity. Little is known about how neurons manage to differentially regulate the release of synaptic vesicles (SVs) and DCVs. To analyze this, we screened all Caenorhabditis elegans Rab GTPases and Tre2/Bub2/Cdc16 (TBC) domain containing GTPase-activating proteins (GAPs) for defects in DCV release from C. elegans motoneurons. rab-5 and rab-10 mutants show severe defects in DCV secretion, whereas SV exocytosis is unaffected. We identified TBC-2 and TBC-4 as putative GAPs for RAB-5 and RAB-10, respectively. Multiple Rabs and RabGAPs are typically organized in cascades that confer directionality to membrane-trafficking processes. We show here that the formation of release-competent DCVs requires a reciprocal exclusion cascade coupling RAB-5 and RAB-10, in which each of the two Rabs recruits the other's GAP molecule. This contributes to a separation of RAB-5 and RAB-10 domains at the Golgi-endosomal interface, which is lost when either of the two GAPs is inactivated. Taken together, our data suggest that RAB-5 and RAB-10 cooperate to locally exclude each other at an essential stage during DCV sorting.
神经元从致密核心囊泡 (DCV) 中分泌神经肽,以调节神经元活动。目前对于神经元如何能够有区别地调节突触囊泡 (SV) 和 DCV 的释放知之甚少。为了分析这一点,我们筛选了所有秀丽隐杆线虫 Rab GTPases 和 Tre2/Bub2/Cdc16 (TBC) 结构域包含 GTPase 激活蛋白 (GAP),以研究它们在秀丽隐杆线虫运动神经元中 DCV 释放的缺陷。rab-5 和 rab-10 突变体显示出 DCV 分泌的严重缺陷,而 SV 胞吐作用不受影响。我们确定 TBC-2 和 TBC-4 分别为 RAB-5 和 RAB-10 的假定 GAP。多个 Rab 和 RabGAP 通常组织在级联中,为膜运输过程提供方向性。我们在这里表明,具有释放能力的 DCV 的形成需要一种相互排斥的级联反应,将 RAB-5 和 RAB-10 耦联在一起,其中两个 Rab 中的每一个都募集另一个的 GAP 分子。这有助于在高尔基内体界面处分离 RAB-5 和 RAB-10 结构域,当两个 GAP 中的任何一个失活时,该结构域就会丢失。总之,我们的数据表明,RAB-5 和 RAB-10 合作,在 DCV 分拣的一个重要阶段相互排斥。