TY - JOUR
T1 - In Vivo gene transfer of dominant-negative Rho-kinase induces regression of coronary arteriosclerosis in pigs
AU - Morishige, Kunio
AU - Shimokawa, Hiroaki
AU - Eto, Yasuhiro
AU - Hoshijima, Masahiko
AU - Kaibuchi, Kozo
AU - Takeshita, Akira
PY - 2001
Y1 - 2001
N2 - Small GTPase Rho and its target Rho-kinase play an important role in various cellular functions that may be involved in the pathogenesis of arteriosclerosis. Here we show that adenovirus-mediated transfer of dominant-negative Rho-kinase (AdDNRhoK) induces a regression of coronary constrictive remodeling and abolishes coronary vasospastic activity in vivo. Porcine coronary segments were chronically treated with interleukin-1β, which resulted in the development of constrictive remodeling and vasospastic responses to serotonin in vivo. AdDNRhoK, but not that of β-galactosidase, into the interleukin-1β-treated coronary segment caused regression of constrictive remodeling and abolished vasospastic activity in 3 weeks. The unregulated phosphorylation of the target proteins of Rho-kinase at the coronary lesion was significantly suppressed by AdDNRhoK. These results indicate that Rho-kinase is substantially involved in the mechanism of coronary arteriosclerosis, which can be reversed by selective inhibition of the molecule in our porcine model in vivo.
AB - Small GTPase Rho and its target Rho-kinase play an important role in various cellular functions that may be involved in the pathogenesis of arteriosclerosis. Here we show that adenovirus-mediated transfer of dominant-negative Rho-kinase (AdDNRhoK) induces a regression of coronary constrictive remodeling and abolishes coronary vasospastic activity in vivo. Porcine coronary segments were chronically treated with interleukin-1β, which resulted in the development of constrictive remodeling and vasospastic responses to serotonin in vivo. AdDNRhoK, but not that of β-galactosidase, into the interleukin-1β-treated coronary segment caused regression of constrictive remodeling and abolished vasospastic activity in 3 weeks. The unregulated phosphorylation of the target proteins of Rho-kinase at the coronary lesion was significantly suppressed by AdDNRhoK. These results indicate that Rho-kinase is substantially involved in the mechanism of coronary arteriosclerosis, which can be reversed by selective inhibition of the molecule in our porcine model in vivo.
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U2 - 10.1111/j.1749-6632.2001.tb03974.x
DO - 10.1111/j.1749-6632.2001.tb03974.x
M3 - Article
C2 - 11795302
AN - SCOPUS:0035680464
SN - 0077-8923
VL - 947
SP - 407
EP - 411
JO - Annals of the New York Academy of Sciences
JF - Annals of the New York Academy of Sciences
ER -