BMP and FGF regulate the differentiation of multipotential pericardial mesoderm into the myocardial or epicardial lineage

被引:133
作者
Kruithof, Boudewijn P. T.
van Wijk, Bram
Somi, Semir
Kruithof-de Julio, Marianna
Perez Pomares, Jos Maria
Weesie, Frank
Wessels, Andy
Moorman, Antoon F. M.
van den Hoff, Maurice J. B.
机构
[1] Acad Med Ctr, Expt & Mol Cardiol Grp, NL-1105 AZ Amsterdam, Netherlands
[2] Acad Med Ctr, Dept Anat & Embryol, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Malaga, Dept Anim Biol, Fac Sci, E-29071 Malaga, Spain
[4] Med Univ S Carolina, Charleston, SC 29425 USA
关键词
cardiovascular development; proepicardium; cardiomyogenesis; cell lineage; bone morphogenetic protein; fibroblast growth factor; chicken;
D O I
10.1016/j.ydbio.2006.03.033
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proepicardial cells give rise to epicardium, coronary vasculature and cardiac fibroblasts. The proepicardium is derived from the mesodermal lining of the prospective pericardial cavity that simultaneously contributes myocardium to the venous pole of the elongating primitive heart tube. Using proepicardial explant cultures, we show that proepicardial cells have the potential to differentiate into cardiac muscle cells, reflecting the multipotency of this pericardial mesoderm. The differentiation into the myocardial or epicardial lineage is mediated by the cooperative action of BMP and FGF signaling. BMP2 is expressed in the distal IFT myocardium and stimulates cardiomyocyte formation. FGF2 is expressed in the proepicardium and stimulates differentiation into the epicardial lineage. In the base of the proepicardium, coexpression of BMP2 and FGF2 inhibits both myocardial and epicardial differentiation. We conclude that the epicardial/myocardial lineage decisions are mediated by an extrinsic, inductive mechanism, which is determined by the position of the cells in the pericardial mesoderm. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:507 / 522
页数:16
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