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

doi: 10.1002/dvdy.20162
pmid: 15376321
Connective tissue growth factor expression and Smad signaling during mouse heart development and myocardial infarction
AbstractConnective tissue growth factor (CTGF) is reported to be a target gene of transforming growth factor β (TGFβ) 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/TGFβ 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 TGFβ expression as well as activated forms of TGFβ but not BMP, Smad effector proteins are colocalized exclusively in the fibroblasts of the scar tissue, suggesting possible cooperation between CTGF and TGFβ during the pathological fibrotic response. Developmental Dynamics 231:542–550, 2004. © 2004 Wiley‐Liss, Inc.
- Utrecht University Netherlands
- University of North Carolina at Chapel Hill United States
- University of California, Los Angeles United States
- Lund University Sweden
- Netherlands Heart Institute Netherlands
Male, Aging, Myocardium, Connective Tissue Growth Factor, Myocardial Infarction, Heart, Fibroblasts, Fibrosis, Immunohistochemistry, Mice, Mutant Strains, Cell Line, Immediate-Early Proteins, DNA-Binding Proteins, Mice, Bone Morphogenetic Proteins, Animals, Intercellular Signaling Peptides and Proteins, Heart Atria, RNA, Messenger, Signal Transduction
Male, Aging, Myocardium, Connective Tissue Growth Factor, Myocardial Infarction, Heart, Fibroblasts, Fibrosis, Immunohistochemistry, Mice, Mutant Strains, Cell Line, Immediate-Early Proteins, DNA-Binding Proteins, Mice, Bone Morphogenetic Proteins, Animals, Intercellular Signaling Peptides and Proteins, Heart Atria, RNA, Messenger, Signal Transduction
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