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Santucci, N.

Publications and source records attributed to Santucci, N..

2 recordsLinked to original sources

Characterization of the mesendoderm progenitors in the gastrulating mouse embryo

A population of putative mesendoderm progenitor cells that can contribute cellular descendants to both mesoderm and endoderm lineages is identified. These progenitor cells are localized to the anterior primitive streak and the adjacent epiblast of E7.0-E7.5 mid-to late-gastrula stage embryos. Lineage tracing in vivo revealed that putative mesendoderm progenitors that are marked by Mixl1 and Mesp1 activity contribute descendants to the endoderm layer. Analysis of the role of Mixl1 transcription factor in endoderm differentiation of the mouse epiblast stem cells revealed the choice for endoderm or mesoderm cell fate depends on the timing of activation of Mixl1 upon exit from pluripotency, suggesting Mixl1 function may underpin the divergence of the mesendoderm progenitor to mesoderm and endoderm lineages. The knowledge gained on the spatial, temporal, and lineage attribute of mesendoderm progenitors enriches our mechanistic understanding of germ layer allocation and endoderm differentiation of mesendoderm progenitor in embryonic development and lineage allocation of primed state pluripotent stem cells in vitro.

developmental biology↗

Unraveling the Role of MIXL1 Activation in Endoderm Differentiation of Isogenic Human Induced Pluripotent Stem Cells

Human induced pluripotent stem cells (hiPSC) possess the ability to differentiate into a multitude of cell and tissue types but display heterogeneous propensity of differentiation into specific lineage. Characterization of the transcriptome of eleven hiPSC lines showed that activation of MIXL1 at the early stage of stem cell differentiation correlated with higher efficacy in generating definitive endoderm and advancing differentiation and maturation of endoderm derivatives. Enforced expression of MIXL1 in the endoderm-inefficient hiPSCs enhanced the propensity of endoderm differentiation, suggesting that modulation of key drivers of lineage differentiation can re-wire hiPSC to the desired lineage propensity to generate the requisite stem cell products.

developmental biology↗