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Publication : Sall1 transiently marks undifferentiated heart precursors and regulates their fate.

First Author  Morita Y Year  2016
Journal  J Mol Cell Cardiol Volume  92
Pages  158-62 PubMed ID  26876450
Mgi Jnum  J:251385 Mgi Id  MGI:6101872
Doi  10.1016/j.yjmcc.2016.02.008 Citation  Morita Y, et al. (2016) Sall1 transiently marks undifferentiated heart precursors and regulates their fate. J Mol Cell Cardiol 92:158-62
abstractText  Cardiac progenitor cells (CPCs) are a crucial source of cells in cardiac development and regeneration. However, reported CPCs are heterogeneous, and no gene has been identified to transiently mark undifferentiated CPCs throughout heart development. Here we show that Spalt-like gene 1 (Sall1), a zing-finger transcription factor, is expressed in undifferentiated CPCs giving rise to both left and right ventricles. Sall1 was transiently expressed in precardiac mesoderm contributing to the first heart field (left ventricle precursors) but not in the field itself. Similarly, Sall1 expression was maintained in the second heart field (outflow tract/right ventricle precursors) but not in cardiac cells. In vitro, high levels of Sall1 at mesodermal stages enhanced cardiomyogenesis, whereas its continued expression suppressed cardiac differentiation. Our study demonstrates that Sall1 marks CPCs in an undifferentiated state and regulates cardiac differentiation. These findings provide fundamental insights into CPC maintenance, which can be instrumental for CPC-based regenerative medicine.
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