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Regulation of murine natural killer cell commitment

Natural killer (NK) cells can derive from the same precursors as B and T cells, however, to achieve lineage specificity, several transcription factors need to be activated or annulled. While a few important transcription factors have been identified for NK genesis the mechanisms of how this is achie...

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Autores principales: Huntington, Nicholas D., Nutt, Stephen L., Carotta, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558707/
https://www.ncbi.nlm.nih.gov/pubmed/23386852
http://dx.doi.org/10.3389/fimmu.2013.00014
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author Huntington, Nicholas D.
Nutt, Stephen L.
Carotta, Sebastian
author_facet Huntington, Nicholas D.
Nutt, Stephen L.
Carotta, Sebastian
author_sort Huntington, Nicholas D.
collection PubMed
description Natural killer (NK) cells can derive from the same precursors as B and T cells, however, to achieve lineage specificity, several transcription factors need to be activated or annulled. While a few important transcription factors have been identified for NK genesis the mechanisms of how this is achieved is far from resolved. Adding to the complexity of this, NK cells are found and potentially develop in diverse locations in vivo and it remains to be addressed if a common NK cell precursor seeds diverse niches and how transcription factors may differentially regulate NK cell commitment in distinct microenvironments. Here we will summarize some recent findings in NK cell commitment and discuss how a NK cell transcriptional network might be organized, while addressing some misconceptions and anomalies along the way.
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spelling pubmed-35587072013-02-05 Regulation of murine natural killer cell commitment Huntington, Nicholas D. Nutt, Stephen L. Carotta, Sebastian Front Immunol Immunology Natural killer (NK) cells can derive from the same precursors as B and T cells, however, to achieve lineage specificity, several transcription factors need to be activated or annulled. While a few important transcription factors have been identified for NK genesis the mechanisms of how this is achieved is far from resolved. Adding to the complexity of this, NK cells are found and potentially develop in diverse locations in vivo and it remains to be addressed if a common NK cell precursor seeds diverse niches and how transcription factors may differentially regulate NK cell commitment in distinct microenvironments. Here we will summarize some recent findings in NK cell commitment and discuss how a NK cell transcriptional network might be organized, while addressing some misconceptions and anomalies along the way. Frontiers Media S.A. 2013-01-30 /pmc/articles/PMC3558707/ /pubmed/23386852 http://dx.doi.org/10.3389/fimmu.2013.00014 Text en Copyright © Huntington, Nutt and Carotta. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Immunology
Huntington, Nicholas D.
Nutt, Stephen L.
Carotta, Sebastian
Regulation of murine natural killer cell commitment
title Regulation of murine natural killer cell commitment
title_full Regulation of murine natural killer cell commitment
title_fullStr Regulation of murine natural killer cell commitment
title_full_unstemmed Regulation of murine natural killer cell commitment
title_short Regulation of murine natural killer cell commitment
title_sort regulation of murine natural killer cell commitment
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558707/
https://www.ncbi.nlm.nih.gov/pubmed/23386852
http://dx.doi.org/10.3389/fimmu.2013.00014
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