TY - JOUR
T1 - Chondromodulin-I maintains normal cardiac valves by preventing angiogensis
AU - Hakuno, Daihiko
AU - Kimura, Naritaka
AU - Yoshioka, Masatoyo
AU - Fukuda, Keiichi
PY - 2007/12
Y1 - 2007/12
N2 - We recently identified chondromodulin-I as a crucial antiangiogenic factor for maintaining cardiac valvular function. Normally, avascular cardiac valves from ApoE-/- mice and humans with valvular heart disease showed angiogenesis and increased expression of vascular endothelial cell growth factor and matrix metalloproteinases, with downregulation of chondromodulin-I. Conditioned medium from cultured valvular interstitial cells inhibited tube formation and migration of endothelial cells, and this effect was rescued by chondromodulin-I siRNA. Cardiac valves of chondromodulin-I-knockout mice showed neovascularization, lipid deposition and calcification, indicating early aortic stenosis. These findings implicated chondromodulin-I as a critical factor for maintaining normal cardiac valves by preventing angiogenesis.
AB - We recently identified chondromodulin-I as a crucial antiangiogenic factor for maintaining cardiac valvular function. Normally, avascular cardiac valves from ApoE-/- mice and humans with valvular heart disease showed angiogenesis and increased expression of vascular endothelial cell growth factor and matrix metalloproteinases, with downregulation of chondromodulin-I. Conditioned medium from cultured valvular interstitial cells inhibited tube formation and migration of endothelial cells, and this effect was rescued by chondromodulin-I siRNA. Cardiac valves of chondromodulin-I-knockout mice showed neovascularization, lipid deposition and calcification, indicating early aortic stenosis. These findings implicated chondromodulin-I as a critical factor for maintaining normal cardiac valves by preventing angiogenesis.
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U2 - 10.1016/j.ddmod.2007.09.007
DO - 10.1016/j.ddmod.2007.09.007
M3 - Review article
AN - SCOPUS:46749119054
SN - 1740-6757
VL - 4
SP - 177
EP - 184
JO - Drug Discovery Today: Disease Models
JF - Drug Discovery Today: Disease Models
IS - 4
ER -