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The ion channel CALHM6 controls bacterial infection‐induced cellular cross‐talk at the immunological synapse

Membrane ion channels of the calcium homeostasis modulator (CALHM) family promote cell–cell crosstalk at neuronal synapses via ATP release, where ATP acts as a neurotransmitter. CALHM6, the only CALHM highly expressed in immune cells, has been linked to the induction of natural killer (NK) cell anti...

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Autores principales: Danielli, Sara, Ma, Zhongming, Pantazi, Eirini, Kumar, Amrendra, Demarco, Benjamin, Fischer, Fabian A, Paudel, Usha, Weissenrieder, Jillian, Lee, Robert J, Joyce, Sebastian, Foskett, J Kevin, Bezbradica, Jelena S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068325/
https://www.ncbi.nlm.nih.gov/pubmed/36861806
http://dx.doi.org/10.15252/embj.2022111450
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author Danielli, Sara
Ma, Zhongming
Pantazi, Eirini
Kumar, Amrendra
Demarco, Benjamin
Fischer, Fabian A
Paudel, Usha
Weissenrieder, Jillian
Lee, Robert J
Joyce, Sebastian
Foskett, J Kevin
Bezbradica, Jelena S
author_facet Danielli, Sara
Ma, Zhongming
Pantazi, Eirini
Kumar, Amrendra
Demarco, Benjamin
Fischer, Fabian A
Paudel, Usha
Weissenrieder, Jillian
Lee, Robert J
Joyce, Sebastian
Foskett, J Kevin
Bezbradica, Jelena S
author_sort Danielli, Sara
collection PubMed
description Membrane ion channels of the calcium homeostasis modulator (CALHM) family promote cell–cell crosstalk at neuronal synapses via ATP release, where ATP acts as a neurotransmitter. CALHM6, the only CALHM highly expressed in immune cells, has been linked to the induction of natural killer (NK) cell anti‐tumour activity. However, its mechanism of action and broader functions in the immune system remain unclear. Here, we generated Calhm6 ( −/− ) mice and report that CALHM6 is important for the regulation of the early innate control of Listeria monocytogenes infection in vivo. We find that CALHM6 is upregulated in macrophages by pathogen‐derived signals and that it relocates from the intracellular compartment to the macrophage‐NK cell synapse, facilitating ATP release and controlling the kinetics of NK cell activation. Anti‐inflammatory cytokines terminate CALHM6 expression. CALHM6 forms an ion channel when expressed in the plasma membrane of Xenopus oocytes, where channel opening is controlled by a conserved acidic residue, E119. In mammalian cells, CALHM6 is localised to intracellular compartments. Our results contribute to the understanding of neurotransmitter‐like signal exchange between immune cells that fine‐tunes the timing of innate immune responses.
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spelling pubmed-100683252023-04-04 The ion channel CALHM6 controls bacterial infection‐induced cellular cross‐talk at the immunological synapse Danielli, Sara Ma, Zhongming Pantazi, Eirini Kumar, Amrendra Demarco, Benjamin Fischer, Fabian A Paudel, Usha Weissenrieder, Jillian Lee, Robert J Joyce, Sebastian Foskett, J Kevin Bezbradica, Jelena S EMBO J Articles Membrane ion channels of the calcium homeostasis modulator (CALHM) family promote cell–cell crosstalk at neuronal synapses via ATP release, where ATP acts as a neurotransmitter. CALHM6, the only CALHM highly expressed in immune cells, has been linked to the induction of natural killer (NK) cell anti‐tumour activity. However, its mechanism of action and broader functions in the immune system remain unclear. Here, we generated Calhm6 ( −/− ) mice and report that CALHM6 is important for the regulation of the early innate control of Listeria monocytogenes infection in vivo. We find that CALHM6 is upregulated in macrophages by pathogen‐derived signals and that it relocates from the intracellular compartment to the macrophage‐NK cell synapse, facilitating ATP release and controlling the kinetics of NK cell activation. Anti‐inflammatory cytokines terminate CALHM6 expression. CALHM6 forms an ion channel when expressed in the plasma membrane of Xenopus oocytes, where channel opening is controlled by a conserved acidic residue, E119. In mammalian cells, CALHM6 is localised to intracellular compartments. Our results contribute to the understanding of neurotransmitter‐like signal exchange between immune cells that fine‐tunes the timing of innate immune responses. John Wiley and Sons Inc. 2023-03-02 /pmc/articles/PMC10068325/ /pubmed/36861806 http://dx.doi.org/10.15252/embj.2022111450 Text en © 2023 The Authors. Published under the terms of the CC BY 4.0 license. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Danielli, Sara
Ma, Zhongming
Pantazi, Eirini
Kumar, Amrendra
Demarco, Benjamin
Fischer, Fabian A
Paudel, Usha
Weissenrieder, Jillian
Lee, Robert J
Joyce, Sebastian
Foskett, J Kevin
Bezbradica, Jelena S
The ion channel CALHM6 controls bacterial infection‐induced cellular cross‐talk at the immunological synapse
title The ion channel CALHM6 controls bacterial infection‐induced cellular cross‐talk at the immunological synapse
title_full The ion channel CALHM6 controls bacterial infection‐induced cellular cross‐talk at the immunological synapse
title_fullStr The ion channel CALHM6 controls bacterial infection‐induced cellular cross‐talk at the immunological synapse
title_full_unstemmed The ion channel CALHM6 controls bacterial infection‐induced cellular cross‐talk at the immunological synapse
title_short The ion channel CALHM6 controls bacterial infection‐induced cellular cross‐talk at the immunological synapse
title_sort ion channel calhm6 controls bacterial infection‐induced cellular cross‐talk at the immunological synapse
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068325/
https://www.ncbi.nlm.nih.gov/pubmed/36861806
http://dx.doi.org/10.15252/embj.2022111450
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