Institute of General Physiology, Ulm University, Albert-Einstein Allee 11, 89081, Ulm, Germany.
School of Environment and Life Sciences, University of Salford, The Crescent, M54WT, Salford, United Kingdom.
Sci Rep. 2019 Aug 19;9(1):11973. doi: 10.1038/s41598-019-47741-0.
Exocytosis is the intracellular trafficking step where a secretory vesicle fuses with the plasma membrane to release vesicle content. Actin and microtubules both play a role in exocytosis; however, their interplay is not understood. Here we study the interaction of actin and microtubules during exocytosis in lung alveolar type II (ATII) cells that secrete surfactant from large secretory vesicles. Surfactant extrusion is facilitated by an actin coat that forms on the vesicle shortly after fusion pore opening. Actin coat compression allows hydrophobic surfactant to be released from the vesicle. We show that microtubules are localized close to actin coats and stay close to the coats during their compression. Inhibition of microtubule polymerization by colchicine and nocodazole affected the kinetics of actin coat formation and the extent of actin polymerisation on fused vesicles. In addition, microtubule and actin cross-linking protein IQGAP1 localized to fused secretory vesicles and IQGAP1 silencing influenced actin polymerisation after vesicle fusion. This study demonstrates that microtubules can influence actin coat formation and actin polymerization on secretory vesicles during exocytosis.
胞吐作用是细胞内运输的一个步骤,在此过程中,分泌囊泡与质膜融合以释放囊泡内容物。肌动蛋白和微管都在胞吐作用中发挥作用;然而,它们的相互作用尚不清楚。在这里,我们研究了肺肺泡 II 型 (ATII) 细胞在胞吐作用期间肌动蛋白和微管的相互作用,这些细胞从大型分泌囊泡中分泌表面活性剂。表面活性剂的挤出是通过融合孔打开后不久在囊泡上形成的肌动蛋白涂层来促进的。肌动蛋白涂层的压缩允许疏水性表面活性剂从囊泡中释放。我们表明,微管定位于肌动蛋白涂层附近,并在其压缩过程中保持靠近涂层。长春花碱和诺考达唑抑制微管聚合会影响肌动蛋白涂层形成的动力学和融合囊泡上肌动蛋白聚合的程度。此外,微管和肌动蛋白交联蛋白 IQGAP1 定位于融合的分泌囊泡上,IQGAP1 沉默会影响囊泡融合后的肌动蛋白聚合。这项研究表明,微管可以影响胞吐作用过程中分泌囊泡上的肌动蛋白涂层形成和肌动蛋白聚合。