<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mierzejewska K</submitter><funding>NIDDK NIH HHS</funding><funding>NCRR NIH HHS</funding><pagination>281-90</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3776718</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>32(2)</volume><pubmed_abstract>It has been postulated that the most primitive population of stem cells, Oct4(+)Sca-1(+)Lin(-)CD45(-) very small embryonic-like stem cells (VSELs), differentiate into tissue-committed stem cells in adult mice. However, Oct4(+) VSELs remain quiescent in adult tissues and do not form teratomas. In thi study, we report the characteristics of the VSEL transcriptome by gene set enrichment analysis employing a microarray database established from 20 murine bone marrow-derived, FACS-sorted VSELs in comparison with hematopoietic stem cells and embryonic stem cells. In the Oct4(+) VSELs, we observed the upregulation of tissue-specific gene sets and a gene set encoding the complement-coagulation cascade. By contrast, in the VSELs, we observed the downregulation of genes involved in the UV radiation </pubmed_abstract><journal>International journal of molecular medicine</journal><pubmed_title>Genome-wide analysis of murine bone marrow‑derived very small embryonic-like stem cells reveals that mitogenic growth factor signaling pathways play a crucial role in the quiescence and ageing of these cells.</pubmed_title><pmcid>PMC3776718</pmcid><funding_grant_id>P20 RR018733</funding_grant_id><funding_grant_id>P20RR018733</funding_grant_id><funding_grant_id>R01 DK074720</funding_grant_id><pubmed_authors>Kucia M</pubmed_authors><pubmed_authors>Kang H</pubmed_authors><pubmed_authors>Mierzejewska K</pubmed_authors><pubmed_authors>Kang JW</pubmed_authors><pubmed_authors>Shin DM</pubmed_authors><pubmed_authors>Heo J</pubmed_authors><pubmed_authors>Ratajczak J</pubmed_authors><pubmed_authors>Ratajczak MZ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-wide analysis of murine bone marrow‑derived very small embryonic-like stem cells reveals that mitogenic growth factor signaling pathways play a crucial role in the quiescence and ageing of these cells.</name><description>It has been postulated that the most primitive population of stem cells, Oct4(+)Sca-1(+)Lin(-)CD45(-) very small embryonic-like stem cells (VSELs), differentiate into tissue-committed stem cells in adult mice. However, Oct4(+) VSELs remain quiescent in adult tissues and do not form teratomas. In thi study, we report the characteristics of the VSEL transcriptome by gene set enrichment analysis employing a microarray database established from 20 murine bone marrow-derived, FACS-sorted VSELs in comparison with hematopoietic stem cells and embryonic stem cells. In the Oct4(+) VSELs, we observed the upregulation of tissue-specific gene sets and a gene set encoding the complement-coagulation cascade. By contrast, in the VSELs, we observed the downregulation of genes involved in the UV radiation </description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Aug</publication><modification>2025-04-18T19:50:46.701Z</modification><creation>2019-06-05T19:18:05Z</creation></dates><accession>S-EPMC3776718</accession><cross_references><pubmed>23708325</pubmed><doi>10.3892/ijmm.2013.1389</doi></cross_references></HashMap>