Modulation of apoptosis, proliferation, and p27 expression in a porcine coronary angioplasty model Journal Article


Authors: Roque, M.; Cordon-Cardo, C.; Fuster, V.; Reis, E. D.; Drobnjak, M.; Badimon, J. J.
Article Title: Modulation of apoptosis, proliferation, and p27 expression in a porcine coronary angioplasty model
Abstract: Smooth muscle cell (SMC) proliferation is a prominent feature of intimal hyperplasia after percutaneous coronary interventions. p27 is a critical regulator of cell proliferation. Our aims were to analyze the time course of p27 expression, Ki67 proliferative index, and apoptosis after angioplasty in the porcine coronary artery. We also investigated the effects of rapamycin - an antiproliferative drug - on these events. The expression of p27 and Ki67, and apoptosis were determined in porcine coronary arteries harvested at timed intervals from 1 h to 28 days after angioplasty. A gradual increase in p27 expression was observed from 7 to 28 days. Ki67 expression peaked by 7-14 days after angioplasty. By 21-28 days, Ki67 expression decreased, while p27 reached maximal levels. An early apoptotic response was found by 6 h, followed by a gradual return to baseline. Rapamycin induced a reduction in Ki67 proliferative index (2 ± 0.5%) and an increase in apoptosis (7 ± 1%) versus untreated animals at the 28-day time point (5 ± 1 and 1 ± 0.5%, respectively; P < 0.05). In summary, coronary angioplasty induced a rapid apoptotic response, followed by a progressive increase in proliferation. Later on, as p27 expression increased in the vessel wall, cell proliferation decreased. Modulation of cell cycle progression may be a useful therapeutic approach in the treatment of intimal hyperplasia after angioplasty. © 2000 Elsevier Science Ireland Ltd.
Keywords: immunohistochemistry; controlled study; protein expression; histopathology; pathogenesis; nonhuman; ki 67 antigen; cell proliferation; animal cell; animals; cell cycle proteins; animal tissue; cell cycle; cell division; apoptosis; animal experiment; animal model; time; protein p27; cyclin-dependent kinase inhibitor p27; tumor suppressor proteins; nick end labeling; coronary vessels; rapamycin; swine; p27; microtubule-associated proteins; coronary artery dilatation; restenosis; angioplasty, transluminal, percutaneous coronary; percutaneous transluminal angioplasty; angioplasty; artery intima proliferation; priority journal; article
Journal Title: Atherosclerosis
Volume: 153
Issue: 2
ISSN: 0021-9150
Publisher: Elsevier Inc.  
Date Published: 2000-12-01
Start Page: 315
End Page: 322
Language: English
DOI: 10.1016/s0021-9150(00)00421-4
PUBMED: 11164420
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 18 November 2015 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors