科研成果详情

题名Fog2 is critical for cardiac function and maintenance of coronary vasculature in the adult mouse heart
作者
发表日期2009-06
发表期刊JOURNAL OF CLINICAL INVESTIGATION   影响因子和分区
语种英语
原始文献类型Article
其他关键词SMOOTH-MUSCLE-CELLS ; FIBROBLAST GROWTH FACTOR-2 ; EPICARDIUM-DERIVED CELLS ; VENTRAL MORPHOGENESIS ; TRANSCRIPTION FACTORS ; TUBE FORMATION ; GATA4 ; EXPRESSION ; FAILURE ; ANGIOGENESIS
摘要Aberrant transcriptional regulation contributes to the pathogenesis of both congenital and adult forms of heart disease. While the transcriptional regulator friend of Gata 2 (FOG2) is known to be essential for heart morphogenesis and coronary development, its tissue-specific function has not been previously investigated. Additionally, little is known about the role of FOG2 in the adult heart. Here we used spatiotemporally regulated inactivation of Fog2 to delineate its function in both the embryonic and adult mouse heart. Early cardiomyocyte-restricted loss of Fog2 recapitulated the cardiac and coronary defects of the Fog2 germline murine knockouts. Later cardiomyocyte-restricted loss of Fog2 (Fog2(MC)) did not result in defects in cardiac structure or coronary vessel formation. However, Fog2(MC) adult mice had severely depressed ventricular function and died at 8-14 weeks. Fog2(MC) adult hearts displayed a paucity of coronary vessels, associated with myocardial hypoxia, increased cardiomyocyte apoptosis, and cardiac fibrosis. Induced inactivation of Fog2 in the adult mouse heart resulted in similar phenotypes, as did ablation of the FOG2 interaction with the transcription factor GATA4. Loss of the FOG2 or FOG2-GATA4 interaction altered the expression of a panel of angiogenesis-related genes. Collectively, our data indicate that FOG2 regulates adult heart function and coronary angiogenesis.
资助项目Harvard Stem Cell Institute; American Heart AssociationAmerican Heart Association; NIHUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USA [P50HL074734]; NATIONAL HEART, LUNG, AND BLOOD INSTITUTEUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Heart Lung & Blood Institute (NHLBI) [K08HL076286, P50HL074734, R01HL095712] Funding Source: NIH RePORTER
出版者AMER SOC CLINICAL INVESTIGATION INC
出版地ANN ARBOR
ISSN0021-9738
EISSN1558-8238
卷号119期号:6页码:1462-1476
DOI10.1172/JCI38723
页数15
WOS类目Medicine, Research & Experimental
WOS研究方向Research & Experimental Medicine
WOS记录号WOS:000266601000013
收录类别SCIE ; SCOPUS
URL查看原文
PubMed ID19411759
SCOPUSEID2-s2.0-67651005839
自科自定义期刊分类T2(B)类
通讯作者地址[Pu W. T.]Enders 1254,Children's Hospital Boston,300 Longwood Avenue,United States
Scopus学科分类Medicine (all)
TOP期刊TOP期刊
引用统计
被引频次:59[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符https://kms.wmu.edu.cn/handle/3ETUA0LF/20091
专题基础医学院(机能实验教学中心)_生物科学系
作者单位
1.Enders 1254,Children's Hospital Boston,300 Longwood Avenue,United States;
2.Department of Genetics,Harvard Medical School,United States;
3.Harvard Stem Cell Institute,Harvard University,United States;
4.Department of Biology,Life Science School,Wenzhou Medical College,China;
5.Department of Anesthesiology, Perioperative and Pain Medicine,Children's Hospital Boston,United States;
6.Department of Pediatrics,Department of Biomedical Genetics,University of Rochester Medical Center,United States;
7.Department of Genetics,Albert Einstein College of Medicine,United States;
8.Department of Genetics,Norris Cotton Cancer Center,Dartmouth Medical School,United States
推荐引用方式
GB/T 7714
Zhou, Bin,Ma, Qing,Sek, Won Kong,et al. Fog2 is critical for cardiac function and maintenance of coronary vasculature in the adult mouse heart[J]. JOURNAL OF CLINICAL INVESTIGATION,2009,119(6):1462-1476.
APA Zhou, Bin., Ma, Qing., Sek, Won Kong., Hu, Yongwu., Campbell, Patrick H.., ... & Pu, William T.. (2009). Fog2 is critical for cardiac function and maintenance of coronary vasculature in the adult mouse heart. JOURNAL OF CLINICAL INVESTIGATION, 119(6), 1462-1476.
MLA Zhou, Bin,et al."Fog2 is critical for cardiac function and maintenance of coronary vasculature in the adult mouse heart".JOURNAL OF CLINICAL INVESTIGATION 119.6(2009):1462-1476.

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