转录因子
血管紧张素II
锌指
克鲁佩尔
血管生成
维甲酸
转化生长因子
锌指转录因子
化学
体内
肌肉肥大
癌症研究
细胞生物学
调节器
生物
内分泌学
受体
生物化学
生物技术
基因
作者
Takayuki Shindo,Ichiro Manabe,Yasushi Fukushima,Kazuyuki Tobe,Kenichi Aizawa,Saku Miyamoto,Keiko Kawai‐Kowase,Nobuo Moriyama,Yasushi Imai,Hayato Kawakami,Hiroaki Nishimatsu,Takashi Ishikawa,Toru Suzuki,Hiroyuki Morita,Koji Maemura,Masataka Sata,Yasunobu Hirata,Masayuki Komukai,Hiroyuki Kagechika,Takashi Kadowaki
出处
期刊:Nature Medicine
[Nature Portfolio]
日期:2002-07-08
卷期号:8 (8): 856-863
被引量:392
摘要
We recently isolated a Kruppel-like zinc-finger transcription factor 5 (KLF5; also known as BTEB2 and IKLF), which is markedly induced in activated vascular smooth-muscle cells and fibroblasts. Here we describe our analysis of the in vivo function of KLF5 using heterozygous KLF5-knockout mice (Klf5(+/-)). In response to external stress, Klf5(+/-) mice showed diminished levels of arterial-wall thickening, angiogenesis, cardiac hypertrophy and interstitial fibrosis. Also, angiotensin II induced expression of KLF5, which in turn activated platelet-derived growth factor-A (PDGF-A) and transforming growth factor-beta (TGF-beta) expression. In addition, we determined that KLF5 interacted with the retinoic-acid receptor (RAR), that synthetic RAR ligands modulated KLF5 transcriptional activity, and that in vivo administration of RAR ligands affected stress responses in the cardiovascular system in a KLF5-dependent manner. KLF5 thus seems to be a key element linking external stress and cardiovascular remodeling.
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