Enteric glial <scp>NLRP3</scp> inflammasome contributes to gut mucosal barrier alterations in a mouse model of diet‐induced obesity

HFD intake elicits mucosal enteric gliotic processes characterized by a hyperactivation of NLRP3/caspase-1/IL-1β signaling pathway, that contributes to further exacerbate the disruption of intestinal mucosal barrier integrity. However, we cannot rule out the contribution of NLRP3 inflammasome activation from other cells, such as immune cells, in IEB alterations associated with obesity. Overall, our results suggest that enteric glial NLRP3 inflammasome might represent an interesting molecular target for the development of novel pharmacological approaches aimed at managing the enteric inflammation and intestinal mucosal dysfunctions associated with obesity.

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Publication Details

Journal
Acta Physiologica
Published
2024-09-17
DOI
https://doi.org/10.1111/apha.14232
Citations
8
Primary Topic
Congenital gastrointestinal and neural anomalies
Type
article
Field-Weighted Citation Impact
4.58

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article

Enteric glial NLRP3 inflammasome contributes to gut mucosal barrier alterations in a mouse model of diet‐induced obesity

Cristina Segnani, Clelia Di Salvo, Chiara Ippolito, Nunzia Bernardini et al.
8 citations
Acta Physiologica
Congenital gastrointestinal and neural anomalies
4.58
article

Enteric glial NLRP3 inflammasome contributes to gut mucosal barrier alterations in a mouse model of diet‐induced obesity

Cristina Segnani, Clelia Di Salvo, Chiara Ippolito, Nunzia Bernardini, Anna Nericcio, Vanessa D’Antongiovanni, Matteo Fornai, György Haskó, Luca Antonioli, Rocchina Colucci, Carolina Pellegrini, Laura Benvenuti, Zoltán H. Németh, Clarissa Pierucci
article en
8 citations

Abstract

HFD intake elicits mucosal enteric gliotic processes characterized by a hyperactivation of NLRP3/caspase-1/IL-1β signaling pathway, that contributes to further exacerbate the disruption of intestinal mucosal barrier integrity. However, we cannot rule out the contribution of NLRP3 inflammasome activation from other cells, such as immune cells, in IEB alterations associated with obesity. Overall, our results suggest that enteric glial NLRP3 inflammasome might represent an interesting molecular target for the development of novel pharmacological approaches aimed at managing the enteric inflammation and intestinal mucosal dysfunctions associated with obesity.

Acta PhysiologicaVol. 241(1)
University of Pisa (IT), University of Padua (IT), Columbia University Irving Medical Center (US), Morristown Medical Center (US)
Università di Pisa
Openalex Percentile: Top 5%
Congenital gastrointestinal and neural anomalies
4.58
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