Literature DB >> 20969589

The intrathymic crossroads of T and NK cell differentiation.

Roel G J Klein Wolterink1, Marcos E García-Ojeda, Christian A J Vosshenrich, Rudi W Hendriks, James P Di Santo.   

Abstract

T lymphocytes depend on the thymic microenvironment for initiation of the T-cell developmental program. As the progenitors in the thymus have lost the capacity to self-renew, this process depends on the constant influx of hematopoietic progenitors that originate in the bone marrow. Nevertheless, thymic emigrants are heterogeneous and retain developmental plasticity for both the myeloid and lymphoid lineages. It is the role of the thymic microenvironment to steer these uncommitted progenitors toward a T-cell fate. Still, the thymus also generates a unique population of thymic NK cells, thus raising the question of how the T versus NK lymphoid cell fate is determined intrathymically. Many factors have been implicated in the developmental pathways in the thymus, and the processes are characterized by both subtle and not so subtle modifications in gene expression. In this review, we consider the crucial factors governing lineage determination of T cells versus NK cells from bi-potent thymic NK/T precursors. Recent reports have shed new light on the complex interactions of cytokines and transcription factors at different cell fate decision branch points in thymopoiesis. We discuss the implications of these findings and propose a model that may be applicable at this critical thymic NK/T juncture.
© 2010 John Wiley & Sons A/S.

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Year:  2010        PMID: 20969589     DOI: 10.1111/j.1600-065X.2010.00960.x

Source DB:  PubMed          Journal:  Immunol Rev        ISSN: 0105-2896            Impact factor:   12.988


  18 in total

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Journal:  Immunol Rev       Date:  2010-11       Impact factor: 12.988

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Review 8.  Multilayered specification of the T-cell lineage fate.

Authors:  Ellen V Rothenberg; Jingli Zhang; Long Li
Journal:  Immunol Rev       Date:  2010-11       Impact factor: 12.988

9.  Age-associated changes in the differentiation potentials of human circulating hematopoietic progenitors to T- or NK-lineage cells.

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10.  Essential, dose-dependent role for the transcription factor Gata3 in the development of IL-5+ and IL-13+ type 2 innate lymphoid cells.

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Journal:  Proc Natl Acad Sci U S A       Date:  2013-06-03       Impact factor: 11.205

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