Literature DB >> 10047971

Protein hormone storage in secretory granules: mechanisms for concentration and sorting.

P S Dannies1.   

Abstract

Recent findings in cell biology have demonstrated there are several kinds of active sorting from the trans-Golgi network in all cells. The presence of several sorting pathways, using more than one sorting signal, in neuroendocrine cells means that mutations that direct a hormone to a constitutive pathway instead of a regulated one may not simply be interpreted as a signal for sorting to a regulated pathway. The use of three-dimensional electron microscopy of lactotrophs and the possibility that the trans-Golgi network is consumed during sorting has suggested a major role for hormone aggregation, not only as a sorting mechanism, but also as a mechanism for granule formation, in that other transport vesicles may bud from the trans-Golgi network, leaving the aggregated protein as the dense core granule. If aggregation plays such a role, it is unclear how it works in cases where the prohormone must be processed one or more times; does a porous aggregate or colloid form? Obtaining information about the kinds of aggregates that occur in cells is difficult, because at this time there is not a definitive way of knowing whether an aggregate that occurs in solution also occurs in cells. Although secretory granule proteins tend to aggregate relatively easily in solution, the separate treatment of different secretory granule proteins in the same cell make it unlikely that aggregation is a purely passive process, but suggests that the process of aggregation of each hormone is actively controlled in cells. Even if the ability to aggregate accounts for most of the sorting of cargo-secretory granule proteins into granules, other sorting must still occur to get correct membrane proteins necessary for transport and exocytosis into secretory granule membranes. Possible recognition sites for these secretory granule membrane proteins include the cargo itself in an aggregated form, membrane lipids in some unrecognized way, or the proteins and factors that specifically control aggregation of the cargo.

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Year:  1999        PMID: 10047971     DOI: 10.1210/edrv.20.1.0354

Source DB:  PubMed          Journal:  Endocr Rev        ISSN: 0163-769X            Impact factor:   19.871


  46 in total

1.  New class of cargo protein in Tetrahymena thermophila dense core secretory granules.

Authors:  Alex Haddad; Grant R Bowman; Aaron P Turkewitz
Journal:  Eukaryot Cell       Date:  2002-08

Review 2.  Is there structural specificity in the reversible protein aggregates that are stored in secretory granules?

Authors:  Camille Keeler; Michael E Hodsdon; Priscilla S Dannies
Journal:  J Mol Neurosci       Date:  2004       Impact factor: 3.444

3.  In vitro aggregation of the regulated secretory protein chromogranin A.

Authors:  Renu K Jain; Wen Tzu Chang; Chitta Geetha; Paul B M Joyce; Sven-Ulrik Gorr
Journal:  Biochem J       Date:  2002-12-01       Impact factor: 3.857

Review 4.  Exocytosis in astrocytes: transmitter release and membrane signal regulation.

Authors:  Alenka Guček; Nina Vardjan; Robert Zorec
Journal:  Neurochem Res       Date:  2012-04-21       Impact factor: 3.996

5.  Function suggests nano-structure: electrophysiology supports that granule membranes play dice.

Authors:  Ilan Hammel; Isaac Meilijson
Journal:  J R Soc Interface       Date:  2012-05-23       Impact factor: 4.118

Review 6.  Pathobiology of dynorphins in trauma and disease.

Authors:  Kurt F Hauser; Jane V Aldrich; Kevin J Anderson; Georgy Bakalkin; MacDonald J Christie; Edward D Hall; Pamela E Knapp; Stephen W Scheff; Indrapal N Singh; Bryce Vissel; Amina S Woods; Tatiana Yakovleva; Toni S Shippenberg
Journal:  Front Biosci       Date:  2005-01-01

7.  Lumenal protein sorting to the constitutive secretory pathway of a regulated secretory cell.

Authors:  Roberto Lara-Lemus; Ming Liu; Mark D Turner; Philipp Scherer; Gudrun Stenbeck; Puneeth Iyengar; Peter Arvan
Journal:  J Cell Sci       Date:  2006-04-11       Impact factor: 5.285

8.  Not all secretory granules are created equal: Partitioning of soluble content proteins.

Authors:  Jacqueline A Sobota; Francesco Ferraro; Nils Bäck; Betty A Eipper; Richard E Mains
Journal:  Mol Biol Cell       Date:  2006-09-27       Impact factor: 4.138

9.  Chromogranin A promotes peptide hormone sorting to mobile granules in constitutively and regulated secreting cells: role of conserved N- and C-terminal peptides.

Authors:  Maité Montero-Hadjadje; Salah Elias; Laurence Chevalier; Magalie Benard; Yannick Tanguy; Valérie Turquier; Ludovic Galas; Laurent Yon; Maria M Malagon; Azeddine Driouich; Stéphane Gasman; Youssef Anouar
Journal:  J Biol Chem       Date:  2009-01-29       Impact factor: 5.157

10.  EGFP-tagged vasopressin precursor protein sorting into large dense core vesicles and secretion from PC12 cells.

Authors:  Bing-Jun Zhang; Mitsuo Yamashita; Ray Fields; Kiyoshi Kusano; Harold Gainer
Journal:  Cell Mol Neurobiol       Date:  2005-06       Impact factor: 5.046

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