Development and characterization of a cloned rat pulmonary arterial smooth muscle cell line that maintains differentiated properties through multiple subcultures.
Author(s) -
Abraham Rothman,
Thomas J. Kulik,
Mark B. Taubman,
Bradford C. Berk,
Christopher W. Smith,
Bernardo NadalGinard
Publication year - 1992
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/01.cir.86.6.1977
Subject(s) - myosin , pulmonary artery , contractility , myosin light chain kinase , microbiology and biotechnology , myocyte , population , vascular smooth muscle , calponin , cell type , pulmonary hypertension , medicine , transfection , cell culture , biology , cell , actin , smooth muscle , genetics , environmental health
Pulmonary hypertension is associated with abnormal pulmonary arterial contractility and growth. The mechanisms for these abnormalities are largely unknown. To study these processes, we sought to develop an in vitro system. Even though cultured aortic and pulmonary artery smooth muscle cells (SMCs) have been of considerable value in studying smooth muscle biology, one drawback of this system has been that these cells often lose differentiated properties in an unpredictable manner when they are passaged in culture. In addition, there appear to be significant differences in physiological and pathological responses between the systemic and pulmonary circulations, many of which could be directly related to the smooth muscle. We therefore established a cloned population of rat pulmonary arterial SMCs (PASMCs) that maintain differentiated properties through multiple subcultures.
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