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Rab3D Is Critical for Secretory Granule Maturation in PC12 Cells
Authors:Tanja K?gel  Rüdiger Rudolf  Erlend Hodneland  John Copier  Romano Regazzi  Sharon A. Tooze  Hans-Hermann Gerdes
Affiliation:1. Department of Biomedicine, University of Bergen, Bergen, Norway.; 2. Interdisciplinary Center of Neurobiology, University of Heidelberg, Heidelberg, Germany.; 3. London Research Institute Cancer Research United Kingdom, Lincoln''s Inn Fields Laboratories, London, United Kingdom.; 4. Department of Fundamental Neurosciences, University of Lausanne, Lausanne, Switzerland.; University of Iowa, United States of America,
Abstract:Neuropeptide- and hormone-containing secretory granules (SGs) are synthesized at the trans-Golgi network (TGN) as immature secretory granules (ISGs) and complete their maturation in the F-actin-rich cell cortex. This maturation process is characterized by acidification-dependent processing of cargo proteins, condensation of the SG matrix and removal of membrane and proteins not destined to mature secretory granules (MSGs). Here we addressed a potential role of Rab3 isoforms in these maturation steps by expressing their nucleotide-binding deficient mutants in PC12 cells. Our data show that the presence of Rab3D(N135I) decreases the restriction of maturing SGs to the F-actin-rich cell cortex, blocks the removal of the endoprotease furin from SGs and impedes the processing of the luminal SG protein secretogranin II. This strongly suggests that Rab3D is implicated in the subcellular localization and maturation of ISGs.
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