Connective tissue growth factor expression and Smad signaling during mouse heart development and myocardial infarction

被引:87
作者
Lopes, SMCDS
Feijen, A
Korving, J
Korchynskyi, O
Larsson, J
Karlsson, S
Ten Dijke, P
Lyons, KM
Goldschmeding, R
Doevendans, P
Mummery, CL
机构
[1] Netherlands Inst Dev Biol, Hubrecht Lab, NL-3584 CT Utrecht, Netherlands
[2] Netherlands Canc Inst, Amsterdam, Netherlands
[3] Univ Lund Hosp, Dept Med, S-22185 Lund, Sweden
[4] Univ Lund Hosp, Inst Lab Med, S-22185 Lund, Sweden
[5] Univ Calif Los Angeles, Dept Biol Chem, David Geffen Sch Med, Los Angeles, CA 90024 USA
[6] Univ Calif Los Angeles, Dept Orthopaed Surg, Los Angeles, CA USA
[7] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA USA
[8] Univ Utrecht, Ctr Med, Dept Pathol, Utrecht, Netherlands
[9] Univ Utrecht, Ctr Med, Dept Cardiol, Heart Lung Ctr, Utrecht, Netherlands
[10] Interuniv Cardiol Inst Netherlands, Utrecht, Netherlands
[11] Univ N Carolina, Dept Rheumatol, Thurston Arthrit Res Ctr, Chapel Hill, NC USA
关键词
heart development; mouse; myocardial infarction; CTGF; TGF beta;
D O I
10.1002/dvdy.20162
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Connective tissue growth factor (CTGF) is reported to be a target gene of transforming growth factor beta (TGFbeta) and bone morphogenetic protein (BMP) in vitro. Its physiological role in angiogenesis and skeletogenesis during mouse development has been described recently. Here, we have mapped expression of CTGF mRNA during mouse heart development, postnatal adult life, and after experimental myocardial infarction. Furthermore, we investigated the relationship between CTGF and the BMP/TGFbeta signaling pathway in particular during heart development in mutant mice. Postnatally, CTGF expression in the heart became restricted to the atrium. Strikingly, 1 week after myocardial infarction, when myocytes have disappeared from the infarct zone, CTGF and TGFbeta expression as well as activated forms of TGFbeta but not BMP, Smad effector proteins are colocalized exclusively in the fibroblasts of the scar tissue, suggesting possible cooperation between CTGF and TGFbeta, during the pathological fibrotic response. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:542 / 550
页数:9
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