Literature DB >> 3296913

Similarities and differences among neuroendocrine, exocrine, and endocytic vesicles.

J D Castle, R S Cameron, P Arvan, M von Zastrow, G Rudnick.   

Abstract

Secretory and endocytic vesicles have analogous functions as cyclic carriers between specific cellular compartments. The centrifugally functioning secretory system operates from the Golgi complex, whereas the centripetally functioning endocytic system operates from the cell surface. Further, within polarized epithelial cells the export traffic can be directed to a distinct plasmalemmal domain which distinguishes exocrine from endocrine secretion and import traffic can be directed transcellularly. These shuttle operations involve a special class of lipid-rich, protein-poor membranes that appear to use an inwardly directed H+-translocase activity to varying extents for pH-dependent sorting and for accumulation and concentration of transported molecules. Comparative analyses of purified membrane preparations from exocrine and endocrine sources identify compositional overlap between different types of shuttle membrane. However, the structural elements that specify a particular origin or destination for a given carrier or determine function in storage and stimulus-dependent shuttling remain unknown.

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Year:  1987        PMID: 3296913     DOI: 10.1111/j.1749-6632.1987.tb27230.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  9 in total

1.  Morphometric studies of secretory granule formation in mouse pancreatic acinar cells. Dissecting the early structural changes following pilocarpine injection.

Authors:  I Hammel; O Shor-Hazan; T Eldar; D Amihai; S Lew
Journal:  J Anat       Date:  1999-01       Impact factor: 2.610

Review 2.  Sorting and storage during secretory granule biogenesis: looking backward and looking forward.

Authors:  P Arvan; D Castle
Journal:  Biochem J       Date:  1998-06-15       Impact factor: 3.857

3.  Free concentrations of sodium, potassium and calcium in chromaffin granules.

Authors:  J R Haigh; R Parris; J H Phillips
Journal:  Biochem J       Date:  1989-04-15       Impact factor: 3.857

4.  Cytoplasmic granule formation in mouse pancreatic acinar cells. Evidence for formation of immature granules (condensing vacuoles) by aggregation and fusion of progranules of unit size, and for reductions in membrane surface area and immature granule volume during granule maturation.

Authors:  S Lew; I Hammel; S J Galli
Journal:  Cell Tissue Res       Date:  1994-11       Impact factor: 5.249

5.  Secretion and cell volume regulation by salivary acinar cells from mice lacking expression of the Clcn3 Cl- channel gene.

Authors:  Jorge Arreola; Ted Begenisich; Keith Nehrke; Ha-Van Nguyen; Keerang Park; Linda Richardson; Baoli Yang; Brian C Schutte; Fred S Lamb; James E Melvin
Journal:  J Physiol       Date:  2002-11-15       Impact factor: 5.182

6.  Routing of membrane proteins to large dense core vesicles in PC12 cells.

Authors:  Ruth Marx; Richard E Mains
Journal:  J Mol Neurosci       Date:  2002 Feb-Apr       Impact factor: 3.444

7.  Characterization of phospholipids in insulin secretory granules and mitochondria in pancreatic beta cells and their changes with glucose stimulation.

Authors:  Michael J MacDonald; Lacmbouh Ade; James M Ntambi; Israr-Ul H Ansari; Scott W Stoker
Journal:  J Biol Chem       Date:  2015-03-11       Impact factor: 5.157

8.  Elucidation of a Copper Binding Site in Proinsulin C-peptide and Its Implications for Metal-Modulated Activity.

Authors:  Michael J Stevenson; Samuel E Janisse; Lizhi Tao; Ryan L Neil; Quang D Pham; R David Britt; Marie C Heffern
Journal:  Inorg Chem       Date:  2020-06-08       Impact factor: 5.165

9.  Protein sorting among two distinct export pathways occurs from the content of maturing exocrine storage granules.

Authors:  M von Zastrow; J D Castle
Journal:  J Cell Biol       Date:  1987-12       Impact factor: 10.539

  9 in total

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