UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

The Transcription Factor E4BP4 Is Not Required for Extramedullary Pathways of NK Cell Development

Crotta, S; Gkioka, A; Male, V; Duarte, JH; Davidson, S; Nisoli, I; Brady, HJM; (2014) The Transcription Factor E4BP4 Is Not Required for Extramedullary Pathways of NK Cell Development. Journal of Immunology , 192 (6) pp. 2677-2688. 10.4049/jimmunol.1302765. Green open access

[thumbnail of Male_The transcription factor E4BP4 is not required for extramedullary pathways of NK cell development.pdf]
Preview
Text
Male_The transcription factor E4BP4 is not required for extramedullary pathways of NK cell development.pdf

Download (1MB) | Preview

Abstract

NK cells contribute to antitumor and antiviral immunosurveillance. Their development in the bone marrow (BM) requires the transcription factor E4BP4/NFIL3, but requirements in other organs are less well defined. In this study, we show that CD3−NK1.1+NKp46+CD122+ NK cells of immature phenotype and expressing low eomesodermin levels are found in thymus, spleen, and liver of E4BP4-deficient mice, whereas numbers of mature, eomesoderminhigh conventional NK cells are drastically reduced. E4BP4-deficient CD44+CD25− double-negative 1 thymocytes efficiently develop in vitro into NK cells with kinetics, phenotype, and functionality similar to wild-type controls, whereas no NK cells develop from E4BP4-deficient BM precursors. In E4BP4/Rag-1 double-deficient (DKO) mice, NK cells resembling those in Rag-1–deficient controls are found in similar numbers in the thymus and liver. However, NK precursors are reduced in DKO BM, and no NK cells develop from DKO BM progenitors in vitro. DKO thymocyte precursors readily develop into NK cells, but DKO BM transfers into nude recipients and NK cells in E4BP4/Rag-1/IL-7 triple-KO mice indicated thymus-independent NK cell development. In the presence of T cells or E4BP4-sufficient NK cells, DKO NK cells have a selective disadvantage, and thymic and hepatic DKO NK cells show reduced survival when adoptively transferred into lymphopenic hosts. This correlates with higher apoptosis rates and lower responsiveness to IL-15 in vitro. In conclusion, we demonstrate E4BP4-independent development of NK cells of immature phenotype, reduced fitness, short t1/2, and potential extramedullary origin. Our data identify E4BP4-independent NK cell developmental pathways and a role for E4BP4 in NK cell homeostasis.

Type: Article
Title: The Transcription Factor E4BP4 Is Not Required for Extramedullary Pathways of NK Cell Development
Open access status: An open access version is available from UCL Discovery
DOI: 10.4049/jimmunol.1302765
Publisher version: https://doi.org/10.4049/jimmunol.1302765
Language: English
Additional information: This is an open-access article distributed under the terms of the CC-BY 3.0 Unported license which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Infection and Immunity
URI: https://discovery.ucl.ac.uk/id/eprint/1463128
Downloads since deposit
72Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item