Evidence map›Paper›PMID 41033583›Full record

ArticleThe Journal of nutrition2025

An Integrated Single-Cell Atlas of the Mouse Ileum Links Nutrient Metabolism with Epithelial and Immune Crosstalk.

Yashu Tang, Peiran Lu, Winyoo Chowanadisai, Brenda J Smith, Janeen L Salak-Johnson, Edralin A Lucas, Stephen L Clarke, Tyrrell Conway, Minghua Tang, Dingbo Lin

Abstract read
In one paragraph

Article in The Journal of nutrition, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Yashu TangDepartment of Nutritional Sciences, Oklahoma State University, Stillwater, OK, United States.
Peiran LuDepartment of Nutritional Sciences, Oklahoma State University, Stillwater, OK, United States.
Winyoo ChowanadisaiDepartment of Nutritional Sciences, Oklahoma State University, Stillwater, OK, United States.
Brenda J SmithDepartment of OB-GYN, Indiana University School of Medicine, Indianapolis, IN, United States.
Janeen L Salak-JohnsonDepartment of Large Animal Clinical Sciences, Michigan State University, East Lansing, MI, United States. Electronic address: john8880@msu.edu.
Edralin A LucasDepartment of Nutritional Sciences, Oklahoma State University, Stillwater, OK, United States.
Stephen L ClarkeDepartment of Nutritional Sciences, Oklahoma State University, Stillwater, OK, United States.
Tyrrell ConwayDepartment of Microbiology and Molecular Genetics, Oklahoma State University, Stillwater, OK, United States.
Minghua TangDepartment of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO, United States. Electronic address: Minghua.tang@colostate.edu.
Dingbo LinDepartment of Nutritional Sciences, Oklahoma State University, Stillwater, OK, United States. Electronic address: dingbo.lin@okstate.edu.

Funding

The adolescent microbiome-gut-brain axis as a potential target in opioid abuse disordersP20GM152333 · NIGMS · OKLAHOMA STATE UNIVERSITY STILLWATER · PI TYRRELL CONWAY · 2024 to 2026
$8.7M
NIGMS NIH HHS P20 GM152333
6 · The paper itself

Abstract

backgroundThe ileum integrates nutrient absorption with mucosal immunity, yet its cell-type-specific functions remain poorly defined. Disruption of epithelial or immune pathways contributes to nutrient deficiency, Crohn's disease, and impaired barrier integrity. Single-cell RNA sequencing (scRNA-seq) provides the resolution needed to uncover epithelial differentiation and immune crosstalk that bulk approaches cannot resolve.

objectivesThis study aimed to map ileal cellular heterogeneity and define epithelial differentiation, nutrient metabolism programs, and epithelial-immune interactions relevant to health and disease.

methodsscRNA-seq was performed on ileal cells from 8-wk-old male C57BL/6J mice. Gene expression and clustering were analyzed using Seurat, with pseudotime trajectory, cell-cell communication, and pathway enrichment analyses applied to characterize intestinal dynamics.

resultsA total of 32,076 ileal cells were identified, including 6 epithelial types and multiple immune populations. Enterocyte subclusters showed distinct nutrient-related functions: Ent_C1, C4, C7, and C8 were enriched for vitamin A absorption; Ent_C0, C1, C2 and C7 for carotenoid metabolism; and Ent_C1, C4, C7, C8, and C9 for vitamin B12 absorption. Coexpression of β-carotene oxygenase 2 (Bco2) and IL 18 (Il18) occurred across enterocytes, stem cells, and goblet cells, whereas noncanonical goblet cells exhibited high Bco2-Il18 expression together with signatures of fatty acid metabolism and stress responses. Plasmacytoid dendritic cells were identified as central regulators of immune-epithelial interactions.

conclusionsThis study provides the first integrated single-cell atlas of the mouse ileum, profiling both epithelial and immune cells and revealing nutrient metabolism programs and epithelial-immune crosstalk relevant to intestinal health and disease.

Indexed as

Epithelial CellsIleumIntestinal MucosaNutrientsAnimalsMaleMiceMice, Inbred C57BLSingle-Cell AnalysisNutrientsepithelial–immune crosstalkIL 18single-cell RNA sequencingvitamin Avitamin B12β-carotene oxygenase 2

Identifiers

PMID41033583
PMCPMC12799417

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.