IL-26 from innate lymphoid cells regulates early-life gut epithelial homeostasis by shaping microbiota composition

Animals host symbiotic microbial communities that shape gut health. However, how the host immune system and microbiota interact to regulate epithelial homeostasis, particularly during early development, remains largely unclear. Human interleukin-26 (IL-26) is associated with gut inflammation and has intrinsic bactericidal activity in vitro, yet its in vivo functions are largely unknown, primarily due to its absence in rodents. To examine the role of IL-26 in early life, we used zebrafish and found that gut epithelial cells in il26-/- larvae exhibited increased proliferation, faster turnover, elevated DNA damage, and altered cell population abundance. This epithelial dysregulation occurred independently of the IL-26 canonical receptor and resulted from dysbiosis in il26-/- larvae. Moreover, IL-26 bactericidal activity was conserved in zebrafish, suggesting a potential role of this property in regulating microbiota composition. We further identified innate lymphoid cells (ILCs) as the primary source of IL-26 at this developmental stage. These findings establish IL-26 as a central player in a regulatory circuit linking the microbiota, ILCs, and intestinal epithelial cells to maintain gut homeostasis during early life.

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Publication Details

Journal
The EMBO Journal
Published
2025-10-22
DOI
https://doi.org/10.1038/s44318-025-00588-w
Citations
2
Primary Topic
IL-33, ST2, and ILC Pathways
Type
article
Field-Weighted Citation Impact
1.59

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article

IL-26 from innate lymphoid cells regulates early-life gut epithelial homeostasis by shaping microbiota composition

Patricia Diabangouaya, Rodrigo A. Morales, Gwendoline Gros, Sylvia Brugman et al.
2 citations
The EMBO Journal
IL-33, ST2, and ILC Pathways
1.59
article

IL-26 from innate lymphoid cells regulates early-life gut epithelial homeostasis by shaping microbiota composition

Patricia Diabangouaya, Rodrigo A. Morales, Gwendoline Gros, Sylvia Brugman, Akshai Janardhana Kurup, Pedro P. Hernández, David Pérez-Pascual, Yazan Salloum, Soraya Rabahi, Jean‐Marc Ghigo, Carmen Gloria Feijóo, Eduardo J. Villablanca, Jos Boekhorst, Camila Garcia-Baudino, Keinis Quintero-Castillo
article en
2 citations

Abstract

Animals host symbiotic microbial communities that shape gut health. However, how the host immune system and microbiota interact to regulate epithelial homeostasis, particularly during early development, remains largely unclear. Human interleukin-26 (IL-26) is associated with gut inflammation and has intrinsic bactericidal activity in vitro, yet its in vivo functions are largely unknown, primarily due to its absence in rodents. To examine the role of IL-26 in early life, we used zebrafish and found that gut epithelial cells in il26-/- larvae exhibited increased proliferation, faster turnover, elevated DNA damage, and altered cell population abundance. This epithelial dysregulation occurred independently of the IL-26 canonical receptor and resulted from dysbiosis in il26-/- larvae. Moreover, IL-26 bactericidal activity was conserved in zebrafish, suggesting a potential role of this property in regulating microbiota composition. We further identified innate lymphoid cells (ILCs) as the primary source of IL-26 at this developmental stage. These findings establish IL-26 as a central player in a regulatory circuit linking the microbiota, ILCs, and intestinal epithelial cells to maintain gut homeostasis during early life.

The EMBO JournalVol. 44(23)
Centre National de la Recherche Scientifique (FR), Karolinska University Hospital (SE), Inserm (FR), Institut Pasteur (FR), Université Paris Cité (FR), Université Paris Sciences et Lettres (FR), Karolinska Institutet (SE), Universidad Andrés Bello (CL), Center for Climate and Resilience Research (CL), Génétique et biologie du développement (FR), Institut Curie (FR), Wageningen University & Research (NL)
Biogen, Infrastructures en Biologie Santé et Agronomie, Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Fondation pour la Recherche Médicale, Ministère de l'Enseignement Supérieur et de la Recherche, Centre National de la Recherche Scientifique
Openalex Percentile: Top 14%
IL-33, ST2, and ILC Pathways
1.59
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