Literature DB >> 8910573

The thrombin receptor is present in myoblasts and its expression is repressed upon fusion.

H S Suidan1, S P Niclou, J Dreessen, N Beltraminelli, D Monard.   

Abstract

Cultured myoblasts derived from limb muscle of newborn rats express thrombin receptor immunoreactivity on their surface. Receptor expression is repressed upon myoblast fusion. This is due at least in part to a decrease in the amount of the thrombin receptor mRNA. Addition of thrombin triggers calcium transients only in mono- but not multinucleated muscle cells. Furthermore, thrombin increases the rate of myoblast proliferation that coincides with an activation of mitogen-activated protein kinase. Northern analysis of thrombin receptor mRNA expression in skeletal muscle showed that the transcript is present at a relatively high level at birth, but is almost undetectable in the adult. By in situ hybridization, the mRNA at birth appeared to be present mostly in mononucleated cells grouped in clusters, but not in muscle fibers. Very few nuclei surrounded by a mRNA signal were present on muscle sections of rats 24 days postnatally. These results suggest that the thrombin receptor plays a role in muscle development.

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Year:  1996        PMID: 8910573     DOI: 10.1074/jbc.271.46.29162

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  3 in total

1.  Distinct PAR/IQGAP expression patterns during murine development: implications for thrombin-associated cytoskeletal reorganization.

Authors:  Lisa D Cupit; Valentina A Schmidt; Frederick Miller; Wadie F Bahou
Journal:  Mamm Genome       Date:  2004-08       Impact factor: 2.957

2.  Mast cell tryptase stimulates myoblast proliferation; a mechanism relying on protease-activated receptor-2 and cyclooxygenase-2.

Authors:  Elise Duchesne; Marie-Hélène Tremblay; Claude H Côté
Journal:  BMC Musculoskelet Disord       Date:  2011-10-14       Impact factor: 2.362

3.  Thrombin causes the enrichment of rat brain primary cultures with ependymal cells via protease-activated receptor 1.

Authors:  Felix Tritschler; Radovan Murín; Barbara Birk; Jürgen Berger; Mirna Rapp; Bernd Hamprecht; Stephan Verleysdonk
Journal:  Neurochem Res       Date:  2007-03-31       Impact factor: 4.414

  3 in total

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