| Literature DB >> 27695000 |
Tiago C Luis1, Sidinh Luc1,2,3, Takuo Mizukami1, Hanane Boukarabila1, Supat Thongjuea1,3, Petter S Woll1, Emanuele Azzoni3, Alice Giustacchini1, Michael Lutteropp1,3, Tiphaine Bouriez-Jones1, Harsh Vaidya4, Adam J Mead1, Deborah Atkinson1, Charlotta Böiers5, Joana Carrelha1, Iain C Macaulay1, Roger Patient3, Frederic Geissmann6,7, Claus Nerlov3, Rickard Sandberg8, Marella F T R de Bruijn3, C Clare Blackburn4, Isabelle Godin9, Sten Eirik W Jacobsen1,3,10.
Abstract
The final stages of restriction to the T cell lineage occur in the thymus after the entry of thymus-seeding progenitors (TSPs). The identity and lineage potential of TSPs remains unclear. Because the first embryonic TSPs enter a non-vascularized thymic rudiment, we were able to directly image and establish the functional and molecular properties of embryonic thymopoiesis-initiating progenitors (T-IPs) before their entry into the thymus and activation of Notch signaling. T-IPs did not include multipotent stem cells or molecular evidence of T cell-restricted progenitors. Instead, single-cell molecular and functional analysis demonstrated that most fetal T-IPs expressed genes of and had the potential to develop into lymphoid as well as myeloid components of the immune system. Moreover, studies of embryos deficient in the transcriptional regulator RBPJ demonstrated that canonical Notch signaling was not involved in pre-thymic restriction to the T cell lineage or the migration of T-IPs.Entities:
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Year: 2016 PMID: 27695000 PMCID: PMC5172420 DOI: 10.1038/ni.3576
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606