<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Marchand T</submitter><funding>New York Stem Cell Foundation</funding><funding>Fondation ARC pour la Recherche sur le Cancer</funding><funding>Centre Hospitalier Universitaire de Rennes</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>Norn Group</funding><funding>NHLBI NIH HHS</funding><funding>National Heart, Lung, and Blood Institute</funding><funding>American Society of Hematology</funding><funding>Uehara Memorial Foundation</funding><funding>Philip Foundation</funding><funding>National Institute of General Medical Sciences</funding><funding>Association pour le Développement de l&amp;apos;Hématologie Oncologie</funding><funding>EMBO European Commission FP7</funding><funding>NCI</funding><funding>NIDDK NIH HHS</funding><funding>NCI NIH HHS</funding><funding>Société Française d&amp;apos;Hématologie</funding><funding>NIGMS NIH HHS</funding><funding>New York State Stem Cell Science</funding><funding>Japan Society for the Promotion of Science</funding><pagination>RP101714</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12097789</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13</volume><pubmed_abstract>Skeletal stem cells (SSCs) have been isolated from various tissues, including periosteum and bone marrow, where they exhibit key functions in bone biology and hematopoiesis, respectively. The role of periosteal SSCs (P-SSCs) in bone regeneration and healing has been extensively studied, but their ability to contribute to the bone marrow stroma is still under debate. In the present study, we characterized a mouse whole bone transplantation model that mimics the initial bone marrow necrosis and fatty infiltration seen after injury. Using this model and a lineage tracing approach, we observed the migration of P-SSCs into the bone marrow after transplantation. Once in the bone marrow, P-SSCs are phenotypically and functionally reprogrammed into bone marrow mesenchymal stem cells (BM-MSCs) that</pubmed_abstract><journal>eLife</journal><pubmed_title>Periosteal skeletal stem cells can migrate into the bone marrow and support hematopoiesis after injury.</pubmed_title><pmcid>PMC12097789</pmcid><funding_grant_id>R01HL162584</funding_grant_id><funding_grant_id>R01DK056638-23S1</funding_grant_id><funding_grant_id>R01DK130895</funding_grant_id><funding_grant_id>IIRP C029570A</funding_grant_id><funding_grant_id>T32GM007288-50</funding_grant_id><funding_grant_id>Marie Curie Actions</funding_grant_id><funding_grant_id>R01 DK056638</funding_grant_id><funding_grant_id>R56DK130895</funding_grant_id><funding_grant_id>R56 DK130895</funding_grant_id><funding_grant_id>P30CA013330</funding_grant_id><funding_grant_id>R01 DK130895</funding_grant_id><funding_grant_id>P30 CA013330</funding_grant_id><funding_grant_id>R01 HL162584</funding_grant_id><funding_grant_id>R01 DK112976</funding_grant_id><funding_grant_id>T32 GM007288</funding_grant_id><funding_grant_id>5R01DK056638</funding_grant_id><funding_grant_id>EMBOCOFUND2012</funding_grant_id><pubmed_authors>Pinho S</pubmed_authors><pubmed_authors>Frenette P</pubmed_authors><pubmed_authors>Saint-Vanne J</pubmed_authors><pubmed_authors>Maryanovich M</pubmed_authors><pubmed_authors>Akinnola KE</pubmed_authors><pubmed_authors>Takeishi S</pubmed_authors><pubmed_authors>Gritsman K</pubmed_authors><pubmed_authors>Birbrair A</pubmed_authors><pubmed_authors>Marchand T</pubmed_authors><pubmed_authors>Lamy T</pubmed_authors><pubmed_authors>Tarte K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Periosteal skeletal stem cells can migrate into the bone marrow and support hematopoiesis after injury.</name><description>Skeletal stem cells (SSCs) have been isolated from various tissues, including periosteum and bone marrow, where they exhibit key functions in bone biology and hematopoiesis, respectively. The role of periosteal SSCs (P-SSCs) in bone regeneration and healing has been extensively studied, but their ability to contribute to the bone marrow stroma is still under debate. In the present study, we characterized a mouse whole bone transplantation model that mimics the initial bone marrow necrosis and fatty infiltration seen after injury. Using this model and a lineage tracing approach, we observed the migration of P-SSCs into the bone marrow after transplantation. Once in the bone marrow, P-SSCs are phenotypically and functionally reprogrammed into bone marrow mesenchymal stem cells (BM-MSCs) that</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-05-29T12:47:35.379Z</modification><creation>2026-04-08T04:45:47.119Z</creation></dates><accession>S-EPMC12097789</accession><cross_references><pubmed>40401637</pubmed><doi>10.7554/eLife.101714</doi></cross_references></HashMap>