Gasdermin D‐Mediated Release of IL‐33 Results in Fetal Brain Developmental Abnormalities During Maternal Colitis

Maternal inflammatory bowel disease (IBD) is associated with an increased incidence of autism spectrum disorder in offspring. The mechanism behind this phenomenon remains largely unknown. Here, we found that offspring from colitic dams exhibit increased brain weight. These offspring also show excessive neural stem cell (NSC) proliferation and behavioral deficits. Furthermore, Gsdmd cleavage is elevated in the colonic epithelium of colitic dams. This increase is associated with developmental abnormalities in the fetal brain. Mechanistically, excessive NSC proliferation is driven by increased IL-33 release from the maternal colonic epithelium in a Gsdmd-dependent manner. In contrast, we found no evidence that maternal luminal LPS leakage or increased fetal microglia accounts for this phenotype. Our study demonstrates that excessive pyroptosis in the maternal colonic epithelium leads to neurodevelopmental defects and disrupts neuroimmune homeostasis in the offspring.

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Publication Details

Journal
Advanced Science
Published
2026-04-13
DOI
https://doi.org/10.1002/advs.202523784
Primary Topic
IL-33, ST2, and ILC Pathways
Type
article
Field-Weighted Citation Impact
0.00

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article

Gasdermin D‐Mediated Release of IL‐33 Results in Fetal Brain Developmental Abnormalities During Maternal Colitis

Huiyang Jia, Jie Zhou, Shufen Zhang, Kai Ma
Advanced Science
IL-33, ST2, and ILC Pathways
article

Gasdermin D‐Mediated Release of IL‐33 Results in Fetal Brain Developmental Abnormalities During Maternal Colitis

Huiyang Jia, Jie Zhou, Shufen Zhang, Kai Ma
article en

Abstract

Maternal inflammatory bowel disease (IBD) is associated with an increased incidence of autism spectrum disorder in offspring. The mechanism behind this phenomenon remains largely unknown. Here, we found that offspring from colitic dams exhibit increased brain weight. These offspring also show excessive neural stem cell (NSC) proliferation and behavioral deficits. Furthermore, Gsdmd cleavage is elevated in the colonic epithelium of colitic dams. This increase is associated with developmental abnormalities in the fetal brain. Mechanistically, excessive NSC proliferation is driven by increased IL-33 release from the maternal colonic epithelium in a Gsdmd-dependent manner. In contrast, we found no evidence that maternal luminal LPS leakage or increased fetal microglia accounts for this phenotype. Our study demonstrates that excessive pyroptosis in the maternal colonic epithelium leads to neurodevelopmental defects and disrupts neuroimmune homeostasis in the offspring.

Advanced Science
Nantong University (CN), University of Chinese Academy of Sciences (CN), Institute of Zoology (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Good health and well-being
Openalex Percentile: Top 17%
IL-33, ST2, and ILC Pathways
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