<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>209(8)</volume><submitter>Peaudecerf L</submitter><pubmed_abstract>Thymus transplants can correct deficiencies of the thymus epithelium caused by the complete DiGeorge syndrome or FOXN1 mutations. However, thymus transplants were never used to correct T cell-intrinsic deficiencies because it is generally believed that thymocytes have short intrinsic lifespans. This notion is based on thymus transplantation experiments where it was shown that thymus-resident cells were rapidly replaced by progenitors originating in the bone marrow. In contrast, here we show that neonatal thymi transplanted into interleukin 7 receptor-deficient hosts harbor populations with extensive capacity to self-renew, and maintain continuous thymocyte generation and export. These thymus transplants reconstitute the full diversity of peripheral T cell repertoires one month after surger</pubmed_abstract><journal>The Journal of experimental medicine</journal><pagination>1401-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3420331</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Thymocytes may persist and differentiate without any input from bone marrow progenitors.</pubmed_title><pmcid>PMC3420331</pmcid><pubmed_authors>Vasseur F</pubmed_authors><pubmed_authors>Di Santo JP</pubmed_authors><pubmed_authors>Peaudecerf L</pubmed_authors><pubmed_authors>Galgano A</pubmed_authors><pubmed_authors>Ezine S</pubmed_authors><pubmed_authors>Krenn G</pubmed_authors><pubmed_authors>Lemos S</pubmed_authors><pubmed_authors>Rocha B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Thymocytes may persist and differentiate without any input from bone marrow progenitors.</name><description>Thymus transplants can correct deficiencies of the thymus epithelium caused by the complete DiGeorge syndrome or FOXN1 mutations. However, thymus transplants were never used to correct T cell-intrinsic deficiencies because it is generally believed that thymocytes have short intrinsic lifespans. This notion is based on thymus transplantation experiments where it was shown that thymus-resident cells were rapidly replaced by progenitors originating in the bone marrow. In contrast, here we show that neonatal thymi transplanted into interleukin 7 receptor-deficient hosts harbor populations with extensive capacity to self-renew, and maintain continuous thymocyte generation and export. These thymus transplants reconstitute the full diversity of peripheral T cell repertoires one month after surger</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Jul</publication><modification>2025-04-05T13:04:34.439Z</modification><creation>2019-03-27T00:56:49Z</creation></dates><accession>S-EPMC3420331</accession><cross_references><pubmed>22778388</pubmed><doi>10.1084/jem.20120845</doi></cross_references></HashMap>