Literature DB >> 26025059

Transitory loss of glia and the subsequent modulation in inflammatory cytokines/chemokines regulate paracellular claudin-5 expression in endothelial cells.

Ryan B Camire1, Holly J Beaulac2, Colin L Willis3.   

Abstract

Signaling mechanisms involved in regulating blood-brain barrier (BBB) integrity during central nervous system (CNS) inflammation remain unclear. We show that an imbalance between pro-/anti-inflammatory cytokines/chemokines alters claudin-5 expression. In vivo, gliotoxin-induced changes in glial populations and an imbalance between pro-/anti-inflammatory cytokine/chemokine expression occurred as BBB integrity was compromised. The balance was restored as BBB integrity was re-established. In vitro, TNF-α, IL-6, and MCP-1 induced paracellular claudin-5 expression loss. TNF-α- and IL-6- effects were mediated through the PI3K pathway and IL-10 attenuated TNF-α's effect. This study shows that pro-/anti-inflammatory modulators play a critical role in BBB integrity during CNS inflammation.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Astrocytes; Blood–brain barrier; Chemokine; Claudin-5; Cytokine; Microglia

Mesh:

Substances:

Year:  2015        PMID: 26025059      PMCID: PMC4451216          DOI: 10.1016/j.jneuroim.2015.05.008

Source DB:  PubMed          Journal:  J Neuroimmunol        ISSN: 0165-5728            Impact factor:   3.478


  50 in total

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9.  TNF-α signals through PKCζ/NF-κB to alter the tight junction complex and increase retinal endothelial cell permeability.

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  8 in total

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Journal:  Mycotoxin Res       Date:  2018-07-13       Impact factor: 3.833

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4.  Gliotoxin Aggravates Experimental Autoimmune Encephalomyelitis by Triggering Neuroinflammation.

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Review 7.  Tissue-Nonspecific Alkaline Phosphatase in Central Nervous System Health and Disease: A Focus on Brain Microvascular Endothelial Cells.

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8.  Blood-brain barrier hyperpermeability precedes demyelination in the cuprizone model.

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  8 in total

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