Cargando…
A variable-gain stochastic pooling motif mediates information transfer from receptor assemblies into NF-κB
A myriad of inflammatory cytokines regulate signaling pathways to maintain cellular homeostasis. The IκB kinase (IKK) complex is an integration hub for cytokines that govern nuclear factor κB (NF-κB) signaling. In response to inflammation, IKK is activated through recruitment to receptor-associated...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302133/ https://www.ncbi.nlm.nih.gov/pubmed/34301608 http://dx.doi.org/10.1126/sciadv.abi9410 |
_version_ | 1783726830009712640 |
---|---|
author | Cruz, J. Agustin Mokashi, Chaitanya S. Kowalczyk, Gabriel J. Guo, Yue Zhang, Qiuhong Gupta, Sanjana Schipper, David L. Smeal, Steven W. Lee, Robin E. C. |
author_facet | Cruz, J. Agustin Mokashi, Chaitanya S. Kowalczyk, Gabriel J. Guo, Yue Zhang, Qiuhong Gupta, Sanjana Schipper, David L. Smeal, Steven W. Lee, Robin E. C. |
author_sort | Cruz, J. Agustin |
collection | PubMed |
description | A myriad of inflammatory cytokines regulate signaling pathways to maintain cellular homeostasis. The IκB kinase (IKK) complex is an integration hub for cytokines that govern nuclear factor κB (NF-κB) signaling. In response to inflammation, IKK is activated through recruitment to receptor-associated protein assemblies. How and what information IKK complexes transmit about the milieu are open questions. Here, we track dynamics of IKK complexes and nuclear NF-κB to identify upstream signaling features that determine same-cell responses. Experiments and modeling of single complexes reveal their size, number, and timing relays cytokine-specific control over shared signaling mechanisms with feedback regulation that is independent of transcription. Our results provide evidence for variable-gain stochastic pooling, a noise-reducing motif that enables cytokine-specific regulation and parsimonious information transfer. We propose that emergent properties of stochastic pooling are general principles of receptor signaling that have evolved for constructive information transmission in noisy molecular environments. |
format | Online Article Text |
id | pubmed-8302133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-83021332021-08-06 A variable-gain stochastic pooling motif mediates information transfer from receptor assemblies into NF-κB Cruz, J. Agustin Mokashi, Chaitanya S. Kowalczyk, Gabriel J. Guo, Yue Zhang, Qiuhong Gupta, Sanjana Schipper, David L. Smeal, Steven W. Lee, Robin E. C. Sci Adv Research Articles A myriad of inflammatory cytokines regulate signaling pathways to maintain cellular homeostasis. The IκB kinase (IKK) complex is an integration hub for cytokines that govern nuclear factor κB (NF-κB) signaling. In response to inflammation, IKK is activated through recruitment to receptor-associated protein assemblies. How and what information IKK complexes transmit about the milieu are open questions. Here, we track dynamics of IKK complexes and nuclear NF-κB to identify upstream signaling features that determine same-cell responses. Experiments and modeling of single complexes reveal their size, number, and timing relays cytokine-specific control over shared signaling mechanisms with feedback regulation that is independent of transcription. Our results provide evidence for variable-gain stochastic pooling, a noise-reducing motif that enables cytokine-specific regulation and parsimonious information transfer. We propose that emergent properties of stochastic pooling are general principles of receptor signaling that have evolved for constructive information transmission in noisy molecular environments. American Association for the Advancement of Science 2021-07-23 /pmc/articles/PMC8302133/ /pubmed/34301608 http://dx.doi.org/10.1126/sciadv.abi9410 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Cruz, J. Agustin Mokashi, Chaitanya S. Kowalczyk, Gabriel J. Guo, Yue Zhang, Qiuhong Gupta, Sanjana Schipper, David L. Smeal, Steven W. Lee, Robin E. C. A variable-gain stochastic pooling motif mediates information transfer from receptor assemblies into NF-κB |
title | A variable-gain stochastic pooling motif mediates information transfer from receptor assemblies into NF-κB |
title_full | A variable-gain stochastic pooling motif mediates information transfer from receptor assemblies into NF-κB |
title_fullStr | A variable-gain stochastic pooling motif mediates information transfer from receptor assemblies into NF-κB |
title_full_unstemmed | A variable-gain stochastic pooling motif mediates information transfer from receptor assemblies into NF-κB |
title_short | A variable-gain stochastic pooling motif mediates information transfer from receptor assemblies into NF-κB |
title_sort | variable-gain stochastic pooling motif mediates information transfer from receptor assemblies into nf-κb |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302133/ https://www.ncbi.nlm.nih.gov/pubmed/34301608 http://dx.doi.org/10.1126/sciadv.abi9410 |
work_keys_str_mv | AT cruzjagustin avariablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT mokashichaitanyas avariablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT kowalczykgabrielj avariablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT guoyue avariablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT zhangqiuhong avariablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT guptasanjana avariablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT schipperdavidl avariablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT smealstevenw avariablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT leerobinec avariablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT cruzjagustin variablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT mokashichaitanyas variablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT kowalczykgabrielj variablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT guoyue variablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT zhangqiuhong variablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT guptasanjana variablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT schipperdavidl variablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT smealstevenw variablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb AT leerobinec variablegainstochasticpoolingmotifmediatesinformationtransferfromreceptorassembliesintonfkb |