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Cited by 226

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

An NF-κB Transcription-Factor-Dependent Lineage-Specific Transcriptional Program Promotes Regulatory T Cell Identity and Function

Open access
Oh, Hyunju, Grinberg-Bleyer, Yenkel, Liao, Will, Maloney, Dillon, Wang, Pingzhang, Wu, Zikai, Wang, Jiguang, Bhatt, Dev M., Heise, Nicole, Schmid, Roland M., Hayden, Matthew S., Klein, Ulf, Rabadan, Raul, Ghosh, Sankar·2017·Immunity

Abstract

Summary Both conventional T (Tconv) cells and regulatory T (Treg) cells are activated through ligation of the T cell receptor (TCR) complex, leading to the induction of the transcription factor NF-κB. In Tconv cells, NF-κB regulates expression of genes essential for T cell activation, proliferation and function. However the role of NF-κB in Treg function remains unclear. We conditionally deleted canonical NF-κB members p65 and c-Rel in developing and mature Treg cells and found they have unique but partially redundant roles. c-Rel was critical for thymic Treg development while p65 was essential for mature Treg identity and maintenance of immune tolerance. Transcriptome and NF-κB p65 binding analyses demonstrated a lineage specific, NF-κB-dependent transcriptional program, enabled by enhanced chromatin accessibility. These dual roles of canonical NF-κB in Tconv and Treg cells highlight the functional plasticity of the NF-κB signaling pathway and underscores the need for more selective strategies to therapeutically target NF-κB.

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Metadata

Authors
Oh, H., Grinberg-Bleyer, Y., Liao, W., Maloney, D., Wang, P., Wu, Z., Wang, J., Bhatt, D. M., Heise, N., Schmid, R. M., Hayden, M. S., Klein, U., Rabadan, R., & Ghosh, S.
Venue
Immunity
Publisher
Elsevier BV
Published
2017-09
Volume
47
Issue
3
Pages
450-465.e5
ISSN
1074-7613 (ISSN-L)
OpenAlex
W2752933178
Cited by
226
References
7
FWCI
8.90
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: An NF-κB Transcription-Factor-Dependent Lineage-Specific Transcriptional Program Promotes Regulatory T Cell Identity and Function. https://app.cochat.ai/papers/10.1016/j.immuni.2017.08.010
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Oh, H., Grinberg-Bleyer, Y., Liao, W., Maloney, D., Wang, P., Wu, Z., Wang, J., Bhatt, D. M., Heise, N., Schmid, R. M., Hayden, M. S., Klein, U., Rabadan, R., & Ghosh, S. (2017). An NF-κB Transcription-Factor-Dependent Lineage-Specific Transcriptional Program Promotes Regulatory T Cell Identity and Function. Immunity. https://doi.org/10.1016/j.immuni.2017.08.010

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.