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Maintenance of pluripotency-like signature in the entire ectoderm leads to neural crest stem cell potential.


ABSTRACT: The ability of the pluripotent epiblast to contribute progeny to all three germ layers is thought to be lost after gastrulation. The later-forming neural crest (NC) rises from ectoderm and it remains poorly understood how its exceptionally high stem-cell potential to generate mesodermal- and endodermal-like derivatives is obtained. Here, we monitor transcriptional changes from gastrulation to neurulation using single-cell-Multiplex-Spatial-Transcriptomics (scMST) complemented with RNA-sequencing. We show maintenance of pluripotency-like signature (Nanog, Oct4/PouV, Klf4-positive) in undecided pan-ectodermal stem-cells spanning the entire ectoderm late during neurulation with ectodermal patterning completed only at the end of neurulation when the pluripotency-like signature becomes restricted to NC, challenging our understanding of gastrulation. Furthermore, broad ectodermal pluripotency-like signature is found at multiple axial levels unrelated to the NC lineage the cells later commit to, suggesting a general role in stemness enhancement and proposing a mechanism by which the NC acquires its ability to form derivatives beyond "ectodermal-capacity" in chick and mouse embryos.

SUBMITTER: Pajanoja C 

PROVIDER: S-EPMC10518019 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature

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Maintenance of pluripotency-like signature in the entire ectoderm leads to neural crest stem cell potential.

Pajanoja Ceren C   Hsin Jenny J   Olinger Bradley B   Schiffmacher Andrew A   Yazejian Rita R   Abrams Shaun S   Dapkunas Arvydas A   Zainul Zarin Z   Doyle Andrew D AD   Martin Daniel D   Kerosuo Laura L  

Nature communications 20230923 1


The ability of the pluripotent epiblast to contribute progeny to all three germ layers is thought to be lost after gastrulation. The later-forming neural crest (NC) rises from ectoderm and it remains poorly understood how its exceptionally high stem-cell potential to generate mesodermal- and endodermal-like derivatives is obtained. Here, we monitor transcriptional changes from gastrulation to neurulation using single-cell-Multiplex-Spatial-Transcriptomics (scMST) complemented with RNA-sequencing  ...[more]

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