Literature DB >> 8615761

Formation of secretory vesicles in permeabilized cells: a salt extract from yeast membranes promotes budding of nascent secretory vesicles from the trans-Golgi network of endocrine cells.

W L Ling1, D Shields.   

Abstract

The mechanism of secretory-vesicle formation from the trans-Golgi network (TGN) of endocrine cells is poorly understood. To identify cytosolic activities that facilitate the formation and fission of nascent secretory vesicles, we treated permeabilized pituitary GH3 cells with high salt to remove endogenous budding factors. Using this cell preparation, secretory-vesicle budding from the TGN required addition of exogenous cytosol and energy. Mammalian cytosols (GH3 cells and bovine brain) promoted post-TGN vesicle formation. Most significantly, a salt extract of membranes from the yeast Saccharomyces cerevisiae, a cell lacking a regulated secretory pathway, stimulated secretory vesicle budding in the absence of mammalian cytosolic factors. These results demonstrate that the factors which promote secretory-vesicle release from the TGN are conserved between yeast and mammalian cells.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8615761      PMCID: PMC1217116          DOI: 10.1042/bj3140723

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  18 in total

1.  Semi-intact cells permeable to macromolecules: use in reconstitution of protein transport from the endoplasmic reticulum to the Golgi complex.

Authors:  C J Beckers; D S Keller; W E Balch
Journal:  Cell       Date:  1987-08-14       Impact factor: 41.582

2.  Secretory granule content proteins and the luminal domains of granule membrane proteins aggregate in vitro at mildly acidic pH.

Authors:  V Colomer; G A Kicska; M J Rindler
Journal:  J Biol Chem       Date:  1996-01-05       Impact factor: 5.157

Review 3.  Mechanisms of intracellular protein transport.

Authors:  J E Rothman
Journal:  Nature       Date:  1994-11-03       Impact factor: 49.962

4.  ATP-dependent inositide phosphorylation required for Ca(2+)-activated secretion.

Authors:  J C Hay; P L Fisette; G H Jenkins; K Fukami; T Takenawa; R A Anderson; T F Martin
Journal:  Nature       Date:  1995-03-09       Impact factor: 49.962

5.  Direct identification of prohormone conversion site in insulin-secreting cells.

Authors:  L Orci; M Ravazzola; M Amherdt; O Madsen; J D Vassalli; A Perrelet
Journal:  Cell       Date:  1985-09       Impact factor: 41.582

Review 6.  Vesicle fusion from yeast to man.

Authors:  S Ferro-Novick; R Jahn
Journal:  Nature       Date:  1994-07-21       Impact factor: 49.962

7.  Prosomatostatin processing in permeabilized cells. Calcium is required for prohormone cleavage but not formation of nascent secretory vesicles.

Authors:  C D Austin; D Shields
Journal:  J Biol Chem       Date:  1996-01-12       Impact factor: 5.157

8.  Prosomatostatin processing in pituitary GH3 cells. Identification and secretion of the intact propeptide.

Authors:  A Elgort; D Shields
Journal:  J Biol Chem       Date:  1994-12-02       Impact factor: 5.157

9.  A role for phosphatidylinositol transfer protein in secretory vesicle formation.

Authors:  M Ohashi; K Jan de Vries; R Frank; G Snoek; V Bankaitis; K Wirtz; W B Huttner
Journal:  Nature       Date:  1995-10-12       Impact factor: 49.962

10.  Prohormone processing in the trans-Golgi network: endoproteolytic cleavage of prosomatostatin and formation of nascent secretory vesicles in permeabilized cells.

Authors:  H Xu; D Shields
Journal:  J Cell Biol       Date:  1993-09       Impact factor: 10.539

View more
  2 in total

1.  Regulation of the formation and trafficking of vesicles from Golgi by PCH family proteins during chemotaxis.

Authors:  S Lee; J W Han; L Leeper; J S Gruver; C Y Chung
Journal:  Biochim Biophys Acta       Date:  2009-05-03

2.  Formation of nascent secretory vesicles from the trans-Golgi network of endocrine cells is inhibited by tyrosine kinase and phosphatase inhibitors.

Authors:  C D Austin; D Shields
Journal:  J Cell Biol       Date:  1996-12       Impact factor: 10.539

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.