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      Epicardial mesothelial cells synthesize and release endothelin.

      Journal of Cardiovascular Pharmacology
      Angiotensin II, toxicity, Animals, Antibodies, Monoclonal, Blotting, Northern, Cell Division, drug effects, Cells, Cultured, Chromatography, High Pressure Liquid, Cross Reactions, Dose-Response Relationship, Drug, Endothelins, biosynthesis, genetics, Epithelial Cells, Epithelium, metabolism, ultrastructure, Gene Expression Regulation, Heart Ventricles, cytology, Male, Microscopy, Electron, Nucleic Acid Hybridization, Pericardium, RNA, Messenger, Radioimmunoassay, Rats, Rats, Sprague-Dawley

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          Abstract

          Adult rat ventricular cardiocytes, when cocultured with epicardial mesothelial cells (EMC), demonstrate remarkable plasticity of phenotype accompanied by a significant increase in cardiocyte contractile protein content, suggesting that a factor with growth-promoting properties may take part in EMC-adult rat ventricular cardiocyte interactions. Endothelin (ET) has been shown to induce cell hypertrophy, including enhancement of expression of muscle-specific genes. We investigated the ability of EMC to synthesize and release ET. By light microscopy, specific immunostaining, with either ET-1 or Big ET-1 antibodies, was visualized in EMC as a fine punctate distributed throughout the cytoplasm. Reverse phase-high performance liquid chromatography (HPLC) of epicardial mesothelial cells conditioned medium showed several peaks of immunoreactive ET. The major peak eluted with the same retention time as that of ET-1. By Northern blot analysis, a specific 2.3-kilobase (kb) mRNA species was detected by hybridization to a cDNA insert encoding for rat prepro-ET-1. ET accumulated in the culture medium in a time-dependent manner, whereas cell content remained comparatively low. Angiotensin II (AII) dose-dependently stimulated release of immunoreactive ET into the culture medium.

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