AI Article Synopsis

  • Researchers used temporal microarray profiles to identify genes linked to PE and Epi differentiation, revealing that Wnt signaling is crucial in determining distinct heart cell lineages.
  • The study found that Wnt inhibitory factor-1 (Wif1) promotes cardiomyocyte differentiation and expands the population of cardiac progenitor cells in chicken embryos, indicating its potential role in enhancing heart development.

Article Abstract

During chicken cardiac development the proepicardium (PE) forms the epicardium (Epi), which contributes to several non-myocardial lineages within the heart. In contrast to Epi-explant cultures, PE explants can differentiate into a cardiomyocyte phenotype. By temporal microarray expression profiles of PE-explant cultures and maturing Epi cells, we identified genes specifically associated with differentiation towards either of these lineages and genes that are associated with the Epi-lineage restriction. We found a central role for Wnt signaling in the determination of the different cell lineages. Immunofluorescent staining after recombinant-protein incubation in PE-explant cultures indicated that the early upregulated Wnt inhibitory factor-1 (Wif1), stimulates cardiomyocyte differentiation in a similar manner as Wnt stimulation. Concordingly, in the mouse pluripotent embryogenic carcinoma cell line p19cl6, early and late Wif1 exposure enhances and attenuates differentiation, respectively. In ovo exposure of the HH12 chicken embryonic heart to Wif1 increases the Tbx18-positive cardiac progenitor pool. These data indicate that Wif1 enhances cardiomyogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001492PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0015504PLOS

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