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(Circulation Research. 2009;105:842.)
© 2009 American Heart Association, Inc.

Molecular Medicine

Tbx1 Regulates Proliferation and Differentiation of Multipotent Heart Progenitors

Li Chen, Filomena Gabriella Fulcoli, Susan Tang, Antonio Baldini

From the Institute of Biosciences and Technology (L.C., S.T., A.B.), Texas A&M University Health Science Center, Houston; Program in Cardiovascular Sciences (L.C.), Baylor College of Medicine, Houston, Tex; University Federico II (A.B.), Naples, Italy; Telethon Institute of Genetics and Medicine (A.B.), Naples, Italy; and Institute of Genetics and Biophysics (F.G.F., A.B.), Consiglio Nazionale delle Ricerche, Naples, Italy.

Correspondence to Antonio Baldini, Institute of Genetics and Biophysics, National Research Council, Via Pietro Castellino, 111, 80131 Napoli, Italy. E-mail baldini{at}igb.cnr.it

Rationale: TBX1 encodes a T-box transcription factor implicated in DiGeorge syndrome, which affects the development of many organs, including the heart. Loss of Tbx1 results into hypoplasia of heart regions derived from the second heart field, a population of cardiac progenitors cells (CPCs). Thus, we hypothesized that Tbx1 is an important player in the biology of CPCs.

Objective: We asked whether Tbx1 is expressed in multipotent CPCs and, if so, what role it may play in them.

Methods and Results: We used clonal analysis of Tbx1-expressing cells and loss and gain of function models, in vivo and in vitro, to define the role of Tbx1 in CPCs. We found that Tbx1 is expressed in multipotent heart progenitors that, in clonal assays, can give rise to 3 heart lineages expressing endothelial, smooth muscle and cardiomyocyte markers. In multipotent cells, Tbx1 stimulates proliferation, explaining why Tbx1^–/– embryos have reduced proliferation in the second heart field. In this population, Tbx1 is expressed while cells are undifferentiated and it disappears with the onset of muscle markers. Loss of Tbx1 results in premature differentiation, whereas gain results in reduced differentiation in vivo. We found that Tbx1 binds serum response factor, a master regulator of muscle differentiation, and negatively regulates its level.

Conclusions: The Tbx1 protein marks CPCs, supports their proliferation, and inhibits their differentiation. We propose that Tbx1 is a key regulator of CPC homeostasis as it modulates positively their proliferation and negatively their differentiation.

Key Words: cardiac progenitor cells • cardiac differentiation • T-box transcription factors • serum response factor