Evidence map›Paper›PMID 40773375›Full record

ArticleDiabetes2025

Molecular Mechanisms of Human Pancreatic Islet Dysfunction Under Overnutrition Metabolic Stress.

Xue Hu, Li Guo, Maria Pilar Toledo, Pamela Sandoval Sanchez, Gengqiang Xie, Chengyang Liu, Ali Naji, Jerome Irianto, Michael G Roper, Yue J Wang

Abstract read
In one paragraph

Article in Diabetes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Xue HuDepartment of Chemistry and Biochemistry, Florida State University, Tallahassee, FL.
Li GuoDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL.
Maria Pilar ToledoDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL.
Pamela Sandoval SanchezDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL.
Gengqiang XieDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL.
Chengyang LiuDepartment of Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA.
Ali NajiDepartment of Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA.
Jerome IriantoDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL.
Michael G RoperDepartment of Chemistry and Biochemistry, Florida State University, Tallahassee, FL.
Yue J WangDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL.ORCID 0000-0003-2641-6904

Funding

The Human Islet Distribution Coordinating Center (UC4)UC4DK098085 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI EVANS-MOLINA, CARMELLA, NILAND, JOYCE CAROL · 2012 to 2017
$25.6M
American Diabetes Association 11-22-JDFPM-03JDRF 1-INO-2022-1129-A-NNIDDK NIH HHS UC4 DK098085
6 · The paper itself

Abstract

Metabolic stress elicits functional changes in pancreatic islets, contributing to the pathogenesis of type 2 diabetes. However, the molecular mechanisms underlying overnutrition stress in islet cells is not well understood. In our study, we subjected human islets to overnutrition with 25 mmol/L glucose and 0.5 mmol/L palmitic acid (glucolipotoxicity) or to a control culture condition with 5.1 mmol/L glucose. We used single-cell RNA sequencing to comprehensively characterize the gene expression changes between these two conditions in a cell type-specific manner. We found that among all islet endocrine cell types, α-cells were the most resilient to glucolipotoxicity, while β-cells were the most susceptible. We also observed a reduction in cell-cell interactions within islet endocrine cells under glucolipotoxicity, alongside alterations in gene regulatory networks linked to type 2 diabetes genetic risk. Finally, targeted drug screening underscored the critical role of histone H3K9 methyltransferases G9a (EHMT2) and GLP (EHMT1) in modulating the β-cell cellular response to overnutrition. ARTICLE HIGHLIGHTS: Glucolipotoxicity disrupts insulin secretion in human islets, yet its cell type-specific impacts and the molecular mechanisms driving these effects remain poorly understood. Single-cell RNA sequencing reveals β-cells as the most sensitive to glucolipotoxicity, with pronounced shifts in the gene regulatory network linked to cellular stress and lineage-specific transcription factors, while α-cells exhibit greater resilience. Cell-cell communications among islet endocrine cells are reduced under glucolipotoxicity. H3K9 methyltransferases G9a and GLP mediate glucolipotoxicity in β-cells. Our study provides a road map of how metabolic stress causally contributes to cellular dysfunction and diabetes pathogenesis.

Indexed as

Insulin-Secreting CellsIslets of LangerhansOvernutritionStress, PhysiologicalDiabetes Mellitus, Type 2Glucagon-Secreting CellsGlucoseHumansInsulin SecretionPalmitic AcidGlucosePalmitic Acid

Identifiers

PMID40773375
PMCPMC12451085

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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.