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(Circulation. 1997;96:2722-2728.)
© 1997 American Heart Association, Inc.
Articles |
From the Cardiovascular Biology Laboratory, Harvard School of Public Health (C.S., W.-S.L., M.E.R., D.Z., D.L.F., E.H.), the Department of Medicine, Harvard Medical School (W.-S.L., M.E.R., E.H.), the Cardiovascular Division, Brigham and Women's Hospital (M.E.R.), and the Cardiac Computer Center, Massachusetts General Hospital (J.B.N.), Boston.
Correspondence to Edgar Haber, MD, Harvard School of Public Health, 677 Huntington Ave, Boston, MA 02115-6028. E-mail haber{at}cvlab.harvard.edu.
Background Hypercholesterolemia is thought to be a significant risk factor for coronary vasculopathy in cardiac transplant recipients.
Methods and Results We examined the development of
arteriosclerosis in mouse carotid artery loops
allografted from B.10A(2R) (H-2h2) donors to
normocholesterolemic C57BL/6J (H-2b)
recipients and hypercholesterolemic C57BL/6J recipients
in which the apolipoprotein (apo) E gene had been knocked out. Luminal
occlusion and cross-sectional neointimal area were greater
in arteries allografted into hypercholesterolemic
recipients at 15 and 30 days after transplantation. We also measured
cellular and extracellular matrix components of the
neointima by computerized planimetry of the fractional
areas subtended by smooth muscle cells (anti
-actin stain),
collagen (Masson's trichrome), lipid (oil red O), and leukocytes
(anti-CD45). The neointimal area stained for smooth muscle
cells was significantly greater in hypercholesterolemic
recipients than in normocholesterolemic recipients at
15 and 30 days after allografting. Lipid contributed to
neointimal area to a lesser degree, and there was no
significant increase in the contribution of collagen or leukocytes.
Conclusions Smooth muscle cell accumulation appears to be the principal contributor to the increase in neointimal area observed in arteries allografted into hypercholesterolemic mice.
Key Words: vasculature transplantation muscle, smooth hypercholesterolemia
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