<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(1)</volume><submitter>Krause MP</submitter><pubmed_abstract>Recent reports of directed reprogramming have raised questions about the stability of cell lineages. Here, we have addressed this issue, focusing upon skin-derived precursors (SKPs), a dermally derived precursor cell. We show by lineage tracing that murine SKPs from dorsal skin originate from mesenchymal and not neural crest-derived cells. These mesenchymally derived SKPs can, without genetic manipulation, generate functional Schwann cells, a neural crest cell type, and are highly similar at the transcriptional level to Schwann cells isolated from the peripheral nerve. This is not a mouse-specific phenomenon, since human SKPs that are highly similar at the transcriptome level can be made from neural crest-derived facial and mesodermally derived foreskin dermis and the foreskin SKPs can make myelinating Schwann cells. Thus, nonneural crest-derived mesenchymal precursors can differentiate into bona fide peripheral glia in the absence of genetic manipulation, suggesting that developmentally defined lineage boundaries are more flexible than widely thought.</pubmed_abstract><journal>Stem cell reports</journal><pagination>85-100</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4110792</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Direct genesis of functional rodent and human schwann cells from skin mesenchymal precursors.</pubmed_title><pmcid>PMC4110792</pmcid><pubmed_authors>Dworski S</pubmed_authors><pubmed_authors>Forrest CR</pubmed_authors><pubmed_authors>Kaplan DR</pubmed_authors><pubmed_authors>Miller FD</pubmed_authors><pubmed_authors>Jones K</pubmed_authors><pubmed_authors>Bagli D</pubmed_authors><pubmed_authors>Peles E</pubmed_authors><pubmed_authors>Paris M</pubmed_authors><pubmed_authors>Feinberg K</pubmed_authors><pubmed_authors>Paul S</pubmed_authors><pubmed_authors>Johnston AP</pubmed_authors><pubmed_authors>Krause MP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Direct genesis of functional rodent and human schwann cells from skin mesenchymal precursors.</name><description>Recent reports of directed reprogramming have raised questions about the stability of cell lineages. Here, we have addressed this issue, focusing upon skin-derived precursors (SKPs), a dermally derived precursor cell. We show by lineage tracing that murine SKPs from dorsal skin originate from mesenchymal and not neural crest-derived cells. These mesenchymally derived SKPs can, without genetic manipulation, generate functional Schwann cells, a neural crest cell type, and are highly similar at the transcriptional level to Schwann cells isolated from the peripheral nerve. This is not a mouse-specific phenomenon, since human SKPs that are highly similar at the transcriptome level can be made from neural crest-derived facial and mesodermally derived foreskin dermis and the foreskin SKPs can make myelinating Schwann cells. Thus, nonneural crest-derived mesenchymal precursors can differentiate into bona fide peripheral glia in the absence of genetic manipulation, suggesting that developmentally defined lineage boundaries are more flexible than widely thought.</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jul</publication><modification>2024-12-04T03:21:50.757Z</modification><creation>2019-03-27T01:32:48Z</creation></dates><accession>S-EPMC4110792</accession><cross_references><pubmed>25068124</pubmed><doi>10.1016/j.stemcr.2014.05.011</doi></cross_references></HashMap>