Sfrp5 identifies murine cardiac progenitors for all myocardial structures except for the right ventricle

Upon acquirement of pulmonary circulation, the ancestral heart may have been remodelled coincidently with, or accompanied by, the production and rearrangement of progenitor cells. However, the progenitor populations that give rise to the left ventricle (LV) and sinus venosus (SV) are still ambiguous...

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Veröffentlicht in:Nature communications 2017-03, Vol.8 (1), p.14664-14664, Article 14664
Hauptverfasser: Fujii, Masayuki, Sakaguchi, Akane, Kamata, Ryo, Nagao, Masataka, Kikuchi, Yutaka, Evans, Silvia M., Yoshizumi, Masao, Shimono, Akihiko, Saga, Yumiko, Kokubo, Hiroki
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Sprache:eng
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Zusammenfassung:Upon acquirement of pulmonary circulation, the ancestral heart may have been remodelled coincidently with, or accompanied by, the production and rearrangement of progenitor cells. However, the progenitor populations that give rise to the left ventricle (LV) and sinus venosus (SV) are still ambiguous. Here we show that the expression of Secreted frizzled-related protein Sfrp5 in the mouse identifies common progenitors for the outflow tract (OFT), LV, atrium and SV but not the right ventricle (RV). Sfrp5 expression begins at the lateral sides of the cardiac crescent, excluding early differentiating regions, and continues in the venous pole, which gives rise to the SV. Lineage-tracing analysis revealed that descendants of Sfrp5 -expressing cells at E7.5 contribute not only to the SV but also to the LV, atria and OFT and are found also in the dorsal splanchnic mesoderm accompanied by the expression of the secondary heart field marker, Islet1 . These findings provide insight into the arrangement of cardiac progenitors for systemic circulation. It is unclear which progenitors define different regions of the heart. Here, the authors find Secreted frizzled-related protein 5 is expressed in murine progenitor cells for the outflow tract, first heart field, and sinus venosus, but not the right ventricle, and Wnt inhibition prevents progenitor proliferation.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms14664