Mast Cell Chymase Induces Apoptosis of Vascular Smooth Muscle Cells
Author(s) -
Markus Leskinen,
Yenfeng Wang,
Dariusz Leszczyński,
Ken A. Lindstedt,
Petri T. Kovanen
Publication year - 2001
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/01.atv.21.4.516
Subject(s) - chymase , apoptosis , tunel assay , terminal deoxynucleotidyl transferase , dna laddering , microbiology and biotechnology , mast cell , vascular smooth muscle , biology , flow cytometry , chemistry , programmed cell death , immunology , endocrinology , biochemistry , smooth muscle , dna fragmentation
—In human coronary atheromas, the numbers of degranulated mast cells and of apoptotic smooth muscle cells (SMCs) are increased. Accordingly, the possibility exists that mast cells participate in the regulation of SMC apoptosis in the lesions. Mast cells isolated from the serosal cavities of rats were stimulated to release their secretory granules. The neutral protease chymase, present in the exocytosed granules, was found to induce apoptosis when added to rat aortic SMCs in culture. The chymase-induced apoptosis of SMCs was detected by flow cytometry, microscopic analysis of cellular morphology, terminal deoxynucleotidyl transferase–mediated dUTP nick end-labeling (TUNEL), and electrophoretic demonstration of DNA laddering. Chymase induced SMC apoptosis in a dose- and time- dependent manner, and its proteolytic activity was essential for the proapoptotic effect. In addition to rat chymase, recombinant human chymase was also found to induce apoptosis of human coronary artery SMCs in culture. These results suggest that mast cells may participate in the apoptotic regulation of SMCs in atherosclerotic lesions.
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