The exosomal miR-26b-3p derived from Crohn’s disease-associated mesenteric adipose tissue induces M1 macrophage polarization and exacerbates ileocolonic anastomosis inflammation via the p38-MAPK signaling pathway

Our findings reveal that exosomal miR-26b-3p drives widespread macrophage inflammation and M1 polarization in hypertrophic MAT-induced ileocolonic anastomosis inflammation via the MAPK pathway.

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Publication Details

Journal
Frontiers in Immunology
Published
2026-02-25
DOI
https://doi.org/10.3389/fimmu.2026.1754302
Primary Topic
Inflammatory Bowel Disease
Type
article
Field-Weighted Citation Impact
0.00
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article

The exosomal miR-26b-3p derived from Crohn’s disease-associated mesenteric adipose tissue induces M1 macrophage polarization and exacerbates ileocolonic anastomosis inflammation via the p38-MAPK signaling pathway

Zhen Guo, Zeqian Yu, X L Zhang, Enhao Wu et al.
Frontiers in Immunology
Inflammatory Bowel Disease
article

The exosomal miR-26b-3p derived from Crohn’s disease-associated mesenteric adipose tissue induces M1 macrophage polarization and exacerbates ileocolonic anastomosis inflammation via the p38-MAPK signaling pathway

Zhen Guo, Zeqian Yu, X L Zhang, Enhao Wu, Lili Gu, Wenwei Qian, Weiming Zhu, Yi Li
article en

Abstract

Our findings reveal that exosomal miR-26b-3p drives widespread macrophage inflammation and M1 polarization in hypertrophic MAT-induced ileocolonic anastomosis inflammation via the MAPK pathway.

Frontiers in ImmunologyVol. 17
Soochow University (TW), Nanjing General Hospital of Nanjing Military Command (CN), Nanjing Maternity and Child Health Care Hospital (CN), Affiliated Hospital of Jining Medical University (CN), Nanjing Medical University (CN), Nanjing University (CN)
Good health and well-being
Openalex Percentile: Top 42%
Inflammatory Bowel Disease
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