Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
Cell. 2014 Nov 20;159(5):1027-1041. doi: 10.1016/j.cell.2014.10.023.
Endocytic cargo and Rab GTPases are segregated to distinct domains of an endosome. These domains maintain their identity until they undergo fission to traffic cargo. It is not fully understood how segregation of cargo or Rab proteins is maintained along the continuous endosomal membrane or what machinery is required for fission. Endosomes form contact sites with the endoplasmic reticulum (ER) that are maintained during trafficking. Here, we show that stable contacts form between the ER and endosome at constricted sorting domains, and free diffusion of cargo is limited at these positions. We demonstrate that the site of constriction and fission for early and late endosomes is spatially and temporally linked to contact sites with the ER. Lastly, we show that altering ER structure and dynamics reduces the efficiency of endosome fission. Together, these data reveal a surprising role for ER contact in defining the timing and position of endosome fission.
内吞货物和 Rab GTPases 被分隔到内体的不同区域。这些区域在发生分裂以运输货物之前保持其身份。目前还不完全清楚如何在内体的连续膜上维持货物或 Rab 蛋白的分离,也不知道分裂所需的机制是什么。内体与内质网(ER)形成接触位点,在运输过程中保持这些接触位点。在这里,我们显示在收缩的分选域之间,ER 和内体之间形成稳定的接触,并且货物的自由扩散在这些位置受到限制。我们证明了早期和晚期内体的收缩和分裂部位在空间和时间上与 ER 接触位点相关。最后,我们表明改变 ER 结构和动力学会降低内体分裂的效率。总之,这些数据揭示了 ER 接触在确定内体分裂的时间和位置方面的惊人作用。