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Physiol. Genomics (May 11, 2004). doi:10.1152/physiolgenomics.00060.2004 Free Article
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Submitted on March 5, 2004
Accepted on May 7, 2004

A Role for Tbx5 in Proepicardial Cell Migration during Cardiogenesis

Cathy J Hatcher1, Nata Y. S.-G. Diman1, Min-Su Kim1, David Pennisi2, Yan Song1, Marsha M Goldstein3, Takashi Mikawa2, and Craig T Basson1*

1 Greenberg Cardiology Division, Department of Medicine, Weill Medical College of Cornell University, New York, NY, USA; Department of Cell and Developmental Biology, Weill Medical College of Cornell University, New York, NY, USA
2 Department of Cell and Developmental Biology, Weill Medical College of Cornell University, New York, NY, USA
3 Department of Pathology, BioReference Laboratories, Elmwood Park, NJ, USA

* To whom correspondence should be addressed. E-mail: ctbasson{at}med.cornell.edu.

Transcriptional regulatory cascades during epicardial and coronary vascular development from proepicardial progenitor cells remain to be defined. We have used immunohistochemistry of human embryonic tissues to demonstrate that the TBX5 transcription factor is expressed not only in the myocardium but also throughout the embryonic epicardium and coronary vasculature. TBX5 is not expressed in other human fetal vascular beds. Furthermore, immunohistochemical analyses of human embryonic tissues reveals that unlike their epicardial counterparts, delaminating epicardial-derived cells do not express TBX5 as they migrate through the subepicardium before undergoing epithelial-mesenchymal transformation required for coronary vasculogenesis. In the chick, Tbx5 is expressed in the embryonic proepicardial organ which is comprised of the epicardial and coronary vascular progenitor cells. Retrovirus-mediated overexpression of human TBX5 inhibits cell incorporation of infected proepicardial cells into the nascent chick epicardium and coronary vasculature. TBX5 overexpression as well as antisensemediated knockdown of chick Tbx5 produce a cell autonomous defect in the proepicardial organ (PEO) that prevents proepicardial cell migration. Thus, both increasing and decreasing Tbx5 dosage impairs development of the proepicardium. Culture of explanted PEOs demonstrates that untreated chick proepicardial cells downregulate Tbx5 expression during cell migration. Therefore, we propose that Tbx5 participates in regulation of proepicardial cell migration, a critical event in the establishment of the epicardium and coronary vasculature.




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