| Literature DB >> 24704266 |
Jian Zou1, Hong Li2, Xi Chen3, Siyu Zeng4, Jiantao Ye2, Changhua Zhou2, Min Liu2, Luankun Zhang2, Na Yu2, Xiaohong Gan5, Houfeng Zhou5, Zhiwei Xian5, Shaorui Chen6, Peiqing Liu7.
Abstract
C/EBPβ, a member of the bHLH gene family of DNA-binding transcription factors, has been indicated as a central signal in physiologic hypertrophy. However, the role of C/EBPβ in pathological cardiac hypertrophy remains to be elucidated. In this study, we revealed that C/EBPβ is involved in cardiac hypertrophy, the expression of C/EBPβ were significantly increased in response to hypertrophic stimulation in vitro and in vivo. C/EBPβ knockdown inhibited PE-induced cardiac hypertrophy, and diminished the nuclear translocation and DNA binding activity of p65-NFκB. These results suggested that C/EBPβ knockdown protected cardiomyocytes from hypertrophy, which may be attributed to inhibition of NFκB-dependent transcriptional activity. These findings shed new light on the understanding of C/EBPβ-related cardiomyopathy, and suggest the potential application of C/EBPβ inhibitors in cardiac hypertrophy.Entities:
Keywords: C/EBPβ; Cardiac hypertrophy; p65-NFκB
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Year: 2014 PMID: 24704266 DOI: 10.1016/j.mce.2014.03.007
Source DB: PubMed Journal: Mol Cell Endocrinol ISSN: 0303-7207 Impact factor: 4.102