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The earliest thymic T cell progenitors sustain B cell and myeloid lineage potential.

TitleThe earliest thymic T cell progenitors sustain B cell and myeloid lineage potential.
Publication TypeJournal Article
Year of Publication2012
AuthorsLuc S, Luis TC, Boukarabila H, Macaulay IC, Buza-Vidas N, Bouriez-Jones T, Lutteropp M, Woll PS, Loughran SJ, Mead AJ, Hultquist A, Brown J, Mizukami T, Matsuoka S, Ferry H, Anderson K, Duarte S, Atkinson D, Soneji S, Domanski A, Farley A, Sanjuan-Pla A, Carella C, Patient R, de Bruijn MFTR, Enver T, Nerlov C, C Blackburn C, Godin I, Jacobsen SEirik W
JournalNat Immunol
Volume13
Issue4
Pagination412-9
Date Published2012 Apr
ISSN1529-2916
KeywordsAnimals, B-Lymphocytes, Cell Lineage, Cell Separation, Flow Cytometry, Hematopoietic Stem Cells, Lymphoid Progenitor Cells, Mice, Mice, Inbred C57BL, Mice, Transgenic, Myeloid Cells, Oligonucleotide Array Sequence Analysis, Precursor Cells, B-Lymphoid, Real-Time Polymerase Chain Reaction, T-Lymphocytes, Thymus Gland
Abstract

The stepwise commitment from hematopoietic stem cells in the bone marrow to T lymphocyte-restricted progenitors in the thymus represents a paradigm for understanding the requirement for distinct extrinsic cues during different stages of lineage restriction from multipotent to lineage-restricted progenitors. However, the commitment stage at which progenitors migrate from the bone marrow to the thymus remains unclear. Here we provide functional and molecular evidence at the single-cell level that the earliest progenitors in the neonatal thymus had combined granulocyte-monocyte, T lymphocyte and B lymphocyte lineage potential but not megakaryocyte-erythroid lineage potential. These potentials were identical to those of candidate thymus-seeding progenitors in the bone marrow, which were closely related at the molecular level. Our findings establish the distinct lineage-restriction stage at which the T cell lineage-commitment process transits from the bone marrow to the remote thymus.

DOI10.1038/ni.2255
Alternate JournalNat. Immunol.
PubMed ID22344248
PubMed Central IDPMC3378629
Grant ListG0501838 / / Medical Research Council / United Kingdom
G0801073 / / Medical Research Council / United Kingdom
G0801073(87511) / / Medical Research Council / United Kingdom
H4RPLK0 / / Medical Research Council / United Kingdom
MC_U137970202 / / Medical Research Council / United Kingdom