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Kruppel-like Factor 15 Regulates Smooth Muscle Response to Vascular Injury—Brief Report
Author(s) -
Yuan Lu,
Saptarsi M. Haldar,
Kevin Croce,
Yunmei Wang,
Mashashi Sakuma,
Toshifumi Morooka,
Baiqiu Wang,
Darwin Jeyaraj,
Susan Gray,
Daniel I. Simon,
Mukesh K. Jain
Publication year - 2010
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.110.207050
Subject(s) - neointima , vascular smooth muscle , regulator , biology , microbiology and biotechnology , medicine , endocrinology , gene , smooth muscle , biochemistry , restenosis , stent
To determine the role of Kruppel-like factor (KLF) 15, a zinc finger transcriptional factor that is expressed in vascular smooth muscle cells (VSMCs) in vascular biology. VSMCs respond to mechanical injury via a tightly orchestrated series of gene regulatory events. KLF15 is broadly expressed in both arterial and venous vascular beds in a VSMC restricted fashion. KLF15 expression is markedly reduced by both pharmacological and mechanical stimuli. To examine the specific role of KLF15 in the vascular response to injury, we performed femoral artery wire injury inKLF15−/− and wild-type mice.KLF15−/− mice develop exaggerated neointimal growth, with evidence of increased SMC proliferation and migration within the neointima. In concordance, gain and loss of function studies in isolated VSMCs demonstrate that KLF15 can directly inhibit SMC proliferation and migration. To our knowledge, these data are the first to identify KLF15 as a novel inhibitor of VSMC proliferation and migration and to implicate this factor as a critical regulator of the vascular response to injury.

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