Epigenetic and transcriptional programming of murine eosinophils in the esophagus

Eosinophils accumulate in different tissues in allergies, cancer, and infectious diseases, adopting distinct properties. Herein, we profiled murine esophageal eosinophils during allergic inflammation using single-cell sequencing, epigenomic mapping, and flow cytometry. Esophageal eosinophils displayed an altered chromatin accessibility profile compared to bone marrow eosinophils, with 761 epi-transcriptionally regulated genes enriched in inflammation, immunoregulation, bacterial sensing, angiogenesis, migration, and apoptosis. The local environment entrains the unique esophageal eosinophil immunophenotype, as suggested by eosinophil-esophageal epithelial co-cultures, esophageal eosinophil transcriptional similarities regardless of the upstream cytokines driving their esophageal localization, and transcription factor gene editing altering esophageal eosinophilia and the associated eosinophil and global esophageal transcriptomes. Finally, the epigenomic and transcriptomic properties of murine esophageal eosinophils are largely conserved in humans. Thus, our data indicate that tissue specialization of esophageal eosinophils is entrained by local environmental cues that induce genome-wide epigenetic reprogramming and regulated by discrete transcription factors and provide a public, epigenetic database of murine tissue eosinophils.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2025-11-25
DOI
https://doi.org/10.1038/s41467-025-65440-5
Citations
1
Primary Topic
Eosinophilic Esophagitis
Type
article
Field-Weighted Citation Impact
2.01

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Epigenetic and transcriptional programming of murine eosinophils in the esophagus

Lee Edsall, Jennifer M. Felton, Ben Wronowski, Netali Ben-Baruch Morgenstern et al.
1 citations
Nature Communications
Eosinophilic Esophagitis
2.01
article

Epigenetic and transcriptional programming of murine eosinophils in the esophagus

Lee Edsall, Jennifer M. Felton, Ben Wronowski, Netali Ben-Baruch Morgenstern, Rana Herro, Andrea M. Klingler, Artem Barski, Julia L.M. Dunn, Michael Kotliar, Mark Rochman, Lydia E. Mack, Tetsuo Shoda, Ty D. Troutman, G. A. Osswald, Matthew T. Weirauch, Julie M. Caldwell, Annalise M. Psaila, Kate Quinlan, Simin Zhang, Marc E. Rothenberg
article en
1 citations

Abstract

Eosinophils accumulate in different tissues in allergies, cancer, and infectious diseases, adopting distinct properties. Herein, we profiled murine esophageal eosinophils during allergic inflammation using single-cell sequencing, epigenomic mapping, and flow cytometry. Esophageal eosinophils displayed an altered chromatin accessibility profile compared to bone marrow eosinophils, with 761 epi-transcriptionally regulated genes enriched in inflammation, immunoregulation, bacterial sensing, angiogenesis, migration, and apoptosis. The local environment entrains the unique esophageal eosinophil immunophenotype, as suggested by eosinophil-esophageal epithelial co-cultures, esophageal eosinophil transcriptional similarities regardless of the upstream cytokines driving their esophageal localization, and transcription factor gene editing altering esophageal eosinophilia and the associated eosinophil and global esophageal transcriptomes. Finally, the epigenomic and transcriptomic properties of murine esophageal eosinophils are largely conserved in humans. Thus, our data indicate that tissue specialization of esophageal eosinophils is entrained by local environmental cues that induce genome-wide epigenetic reprogramming and regulated by discrete transcription factors and provide a public, epigenetic database of murine tissue eosinophils.

Nature CommunicationsVol. 16(1)
Cincinnati Children's Hospital Medical Center (US), UNSW Sydney (AU), University of Cincinnati Medical Center (US)
American Association for the Study of Liver Diseases, Cincinnati Children's Hospital Medical Center, Buckeye Career Center Foundation, Campaign Urging Research for Eosinophilic Disease, National Institutes of Health, Medical Research Council, National Health and Medical Research Council
Openalex Percentile: Top 10%
Eosinophilic Esophagitis
2.01
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.