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CARMA3: Scaffold Protein Involved in NF-κB Signaling

Scaffold proteins are defined as pivotal molecules that connect upstream receptors to specific effector molecules. Caspase recruitment domain protein 10 (CARD10) gene encodes a scaffold protein CARMA3, belongs to the family of CARD and membrane-associated guanylate kinase-like protein (CARMA). Durin...

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Autores principales: Zhang, Shilei, Lin, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381293/
https://www.ncbi.nlm.nih.gov/pubmed/30814996
http://dx.doi.org/10.3389/fimmu.2019.00176
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author Zhang, Shilei
Lin, Xin
author_facet Zhang, Shilei
Lin, Xin
author_sort Zhang, Shilei
collection PubMed
description Scaffold proteins are defined as pivotal molecules that connect upstream receptors to specific effector molecules. Caspase recruitment domain protein 10 (CARD10) gene encodes a scaffold protein CARMA3, belongs to the family of CARD and membrane-associated guanylate kinase-like protein (CARMA). During the past decade, investigating the function of CARMA3 has revealed that it forms a complex with BCL10 and MALT1 to mediate different receptors-dependent signaling, including GPCR and EGFR, leading to activation of the transcription factor NF-κB. More recently, CARMA3 and its partners are also reported to be involved in antiviral innate immune response and DNA damage response. In this review, we summarize the biology of CARMA3 in multiple receptor-induced NF-κB signaling. Especially, we focus on discussing the function of CARMA3 in regulating NF-κB activation and antiviral IFN signaling in the context of recent progress in the field.
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spelling pubmed-63812932019-02-27 CARMA3: Scaffold Protein Involved in NF-κB Signaling Zhang, Shilei Lin, Xin Front Immunol Immunology Scaffold proteins are defined as pivotal molecules that connect upstream receptors to specific effector molecules. Caspase recruitment domain protein 10 (CARD10) gene encodes a scaffold protein CARMA3, belongs to the family of CARD and membrane-associated guanylate kinase-like protein (CARMA). During the past decade, investigating the function of CARMA3 has revealed that it forms a complex with BCL10 and MALT1 to mediate different receptors-dependent signaling, including GPCR and EGFR, leading to activation of the transcription factor NF-κB. More recently, CARMA3 and its partners are also reported to be involved in antiviral innate immune response and DNA damage response. In this review, we summarize the biology of CARMA3 in multiple receptor-induced NF-κB signaling. Especially, we focus on discussing the function of CARMA3 in regulating NF-κB activation and antiviral IFN signaling in the context of recent progress in the field. Frontiers Media S.A. 2019-02-13 /pmc/articles/PMC6381293/ /pubmed/30814996 http://dx.doi.org/10.3389/fimmu.2019.00176 Text en Copyright © 2019 Zhang and Lin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Zhang, Shilei
Lin, Xin
CARMA3: Scaffold Protein Involved in NF-κB Signaling
title CARMA3: Scaffold Protein Involved in NF-κB Signaling
title_full CARMA3: Scaffold Protein Involved in NF-κB Signaling
title_fullStr CARMA3: Scaffold Protein Involved in NF-κB Signaling
title_full_unstemmed CARMA3: Scaffold Protein Involved in NF-κB Signaling
title_short CARMA3: Scaffold Protein Involved in NF-κB Signaling
title_sort carma3: scaffold protein involved in nf-κb signaling
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381293/
https://www.ncbi.nlm.nih.gov/pubmed/30814996
http://dx.doi.org/10.3389/fimmu.2019.00176
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