Literature DB >> 27741412

Pannexin1 as mediator of inflammation and cell death.

Sara Crespo Yanguas1, Joost Willebrords1, Scott R Johnstone2, Michaël Maes1, Elke Decrock3, Marijke De Bock3, Luc Leybaert3, Bruno Cogliati4, Mathieu Vinken5.   

Abstract

Pannexins form channels at the plasma membrane surface that establish a pathway for communication between the cytosol of individual cells and their extracellular environment. By doing so, pannexin signaling dictates several physiological functions, but equally underlies a number of pathological processes. Indeed, pannexin channels drive inflammation by assisting in the activation of inflammasomes, the release of pro-inflammatory cytokines, and the activation and migration of leukocytes. Furthermore, these cellular pores facilitate cell death, including apoptosis, pyroptosis and autophagy. The present paper reviews the roles of pannexin channels in inflammation and cell death. In a first part, a state-of-the-art overview of pannexin channel structure, regulation and function is provided. In a second part, the mechanisms behind their involvement in inflammation and cell death are discussed. Copyright Â
© 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Apoptosis; Autophagy; Inflammation; Pannexin; Pyroptosis

Mesh:

Substances:

Year:  2016        PMID: 27741412      PMCID: PMC5693326          DOI: 10.1016/j.bbamcr.2016.10.006

Source DB:  PubMed          Journal:  Biochim Biophys Acta Mol Cell Res        ISSN: 0167-4889            Impact factor:   4.739


  144 in total

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7.  The ATP permeability of pannexin 1 channels in a heterologous system and in mammalian taste cells is dispensable.

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8.  Pannexin-1-mediated intracellular delivery of muramyl dipeptide induces caspase-1 activation via cryopyrin/NLRP3 independently of Nod2.

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3.  Glial Chloride Channels in the Function of the Nervous System Across Species.

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5.  Apoptotic Osteocytes Induce RANKL Production in Bystanders via Purinergic Signaling and Activation of Pannexin Channels.

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6.  Genetic ablation of pannexin1 counteracts liver fibrosis in a chemical, but not in a surgical mouse model.

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10.  Protective effect of genetic deletion of pannexin1 in experimental mouse models of acute and chronic liver disease.

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