Literature DB >> 6229546

Redistribution of alpha-granules and their contents in thrombin-stimulated platelets.

P E Stenberg, M A Shuman, S P Levine, D F Bainton.   

Abstract

The redistribution of beta-thromboglobulin (beta TG), platelet Factor 4 (PF4), and fibrinogen from the alpha granules of the platelet after stimulation with thrombin was studied by morphologic and immunocytochemical techniques. The use of tannic acid stain and quick-freeze techniques revealed several thrombin-induced morphologic changes. First, the normally discoid platelet became rounder in form, with filopodia, and the granules clustered in its center. The granules then fused with one another and with elements of the surface-connected canalicular system (SCCS) to form large vacuoles in the center of the cell and near the periphery. Neither these vacuoles nor the alpha granules appeared to fuse with the plasma membrane, but the vacuoles were connected to the extracellular space by wide necks, presumably formed by enlargement of the narrow necks connecting the SCCS to the surface of the unstimulated cell. The presence of fibrinogen, beta TG, and PF4 in corresponding large intracellular vacuoles and along the platelet plasma membrane after thrombin stimulation was demonstrated by immunocytochemical techniques in saponin-permeabilized and nonpermeabilized platelets. Immunocytochemical labeling of the three proteins on frozen thin sections of thrombin-stimulated platelets confirmed these findings and showed that all three proteins reached the plasma membrane by the same pathway. We conclude that thrombin stimulation of platelets causes at least some of the fibrinogen, beta TG, and PF4 stored in their alpha granules to be redistributed to their plasma membranes by way of surface-connected vacuoles formed by fusion of the alpha granules with elements of the SCCS.

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Year:  1984        PMID: 6229546      PMCID: PMC2113120          DOI: 10.1083/jcb.98.2.748

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  34 in total

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Journal:  Prog Hemost Thromb       Date:  1974

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Journal:  Lab Invest       Date:  1973-12       Impact factor: 5.662

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Journal:  Am J Pathol       Date:  1968-10       Impact factor: 4.307

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Journal:  J Biol Chem       Date:  1981-09-25       Impact factor: 5.157

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Authors:  D R Phillips; L K Jennings; H R Prasanna
Journal:  J Biol Chem       Date:  1980-12-25       Impact factor: 5.157

7.  Studies of the release from human platelets of the growth factor for cultured human arterial smooth muscle cells.

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Journal:  Circ Res       Date:  1978-03       Impact factor: 17.367

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Authors:  M H Ginsberg; L Taylor; R G Painter
Journal:  Blood       Date:  1980-04       Impact factor: 22.113

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Authors:  G Griffiths; R Brands; B Burke; D Louvard; G Warren
Journal:  J Cell Biol       Date:  1982-12       Impact factor: 10.539

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  53 in total

Review 1.  Platelet surface physiology and its importance in pharmacotherapy design and development: the adenosine diphosphate receptor antagonists.

Authors:  R C Becker
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2.  Immunoelectron-microscopic studies of human platelet thrombospondin, von Willebrand factor, and fibrinogen redistribution during clot formation.

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Journal:  Histochem J       Date:  1990-09

3.  Acquisition of peroxidase activity by rat alveolar macrophages during pulmonary inflammation.

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4.  In vivo defibrination results in markedly decreased amounts of fibrinogen in rat megakaryocytes and platelets.

Authors:  P J Handagama; M A Shuman; D F Bainton
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5.  Osmosensory signaling in Mycobacterium tuberculosis mediated by a eukaryotic-like Ser/Thr protein kinase.

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Journal:  Proc Natl Acad Sci U S A       Date:  2013-12-05       Impact factor: 11.205

6.  Stimulated mobilization of monocyte Mac-1 and p150,95 adhesion proteins from an intracellular vesicular compartment to the cell surface.

Authors:  L J Miller; D F Bainton; N Borregaard; T A Springer
Journal:  J Clin Invest       Date:  1987-08       Impact factor: 14.808

7.  Calpain I remains intact and intracellular during platelet activation. Immunochemical measurements with monoclonal and polyclonal antibodies.

Authors:  J A Samis; G Zboril; J S Elce
Journal:  Biochem J       Date:  1987-09-01       Impact factor: 3.857

8.  Respective contributions of single and compound granule fusion to secretion by activated platelets.

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9.  BIN1 localizes the L-type calcium channel to cardiac T-tubules.

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10.  Endogenous peroxidase activity as a marker of macrophage renewal during BCG-induced inflammation in the rat lung.

Authors:  M L Warnock; M Sniezek; J Shellito
Journal:  Am J Pathol       Date:  1987-07       Impact factor: 4.307

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