Hemalatha Anupama, Prabhakara Chaitra, Mayor Satyajit
Cellular Organization and Signalling, National Centre for Biological Science, Tata Institute for Fundamental Research, Bangalore 560 065, India.
Cellular Organization and Signalling, National Centre for Biological Science, Tata Institute for Fundamental Research, Bangalore 560 065, India;
Proc Natl Acad Sci U S A. 2016 Nov 8;113(45):E6993-E7002. doi: 10.1073/pnas.1610565113. Epub 2016 Oct 25.
Endocytosis of ligand-receptor complexes regulates signal transduction during development. In particular, clathrin and dynamin-dependent endocytosis has been well studied in the context of patterning of the wing disc, wherein apically secreted Wingless (Wg) encounters its receptor, DFrizzled2 (DFz2), resulting in a distinctive dorso-ventral pattern of signaling outputs. Here, we directly track the endocytosis of Wg and DFz2 in the wing disc and demonstrate that Wg is endocytosed from the apical surface devoid of DFz2 via a dynamin-independent CLIC/GEEC pathway, regulated by Arf1, Garz, and class I PI3K. Subsequently, Wg containing CLIC/GEEC endosomes fuse with DFz2-containing vesicles derived from the clathrin and dynamin-dependent endocytic pathway, which results in a low pH-dependent transfer of Wg to DFz2 within the merged and acidified endosome to initiate Wg signaling. The employment of two distinct endocytic pathways exemplifies a mechanism wherein cells in tissues leverage multiple endocytic pathways to spatially regulate signaling.
配体 - 受体复合物的内吞作用在发育过程中调节信号转导。特别是,网格蛋白和发动蛋白依赖性内吞作用在翅盘模式形成的背景下已得到充分研究,其中顶端分泌的无翅蛋白(Wg)与其受体DFrizzled2(DFz2)相遇,导致信号输出呈现独特的背腹模式。在这里,我们直接追踪翅盘中Wg和DFz2的内吞作用,并证明Wg通过由Arf1、Garz和I类磷脂酰肌醇3 - 激酶调节的不依赖发动蛋白的CLIC/GEEC途径从缺乏DFz2的顶端表面内吞。随后,含有Wg的CLIC/GEEC内体与源自网格蛋白和发动蛋白依赖性内吞途径的含有DFz2的囊泡融合,这导致Wg在融合并酸化的内体中以低pH依赖性方式转移至DFz2,从而启动Wg信号传导。两种不同内吞途径的运用例证了一种机制,即组织中的细胞利用多种内吞途径在空间上调节信号传导。