Colonic L-cell impairment in aged subjects with type 2 diabetes leads to diminished GLP-1 production.

Document Type

Article

Publication Date

12-2023

Identifier

DOI: 10.1016/j.dsx.2023.102907

Abstract

AIMS: Glucagon-like peptide 1 (GLP-1) is produced by the L subtype of enteroendocrine cells (EECs). Patients with type 2 diabetes (T2D) exhibit reduced incretin effect, but the pathophysiology and functional change of the L-cells remain unclear. Deciphering the mechanisms of the biological changes in L-cells under T2D conditions may assist in the research of gut-based strategies for T2D therapy.

METHODS: We investigated the fasting serum GLP-1 levels and the distribution of colonic L-cells in young and aged participants with and without T2D. Additionally, we established an aged male T2D Wistar rat model subjected to a long-term high-fat and high-fructose (HFHF) diet. Histological investigations and single-cell RNA sequencing (scRNA-seq) analyses were performed to explore the mechanisms underlying functional changes in the colonic EECs.

RESULTS: We observed a decline in circulating GLP-1 levels and a reduced number of colonic L-cells in elderly patients with T2D. The mechanisms underlying impaired L-cell formation and disturbed GLP-1 production were revealed using aged T2D rats induced by a long-term HFHF diet. The scRNA-seq results showed that the transcription factors that regulate L-cell commitment, such as Foxa1, were downregulated, and the expression of genes that participate in encoding GLP-1, GLP-1 posttranslational processing, hormone secretion, and nutrient sensing was disturbed.

CONCLUSIONS: Taken together, the reduced L-cell lineage commitment and disturbed L-cell functions might be the major cause of the reduced GLP-1 production in aged populations with T2D. Our study provides new insights for identifying novel targets in colonic L-cells for improving endogenous GLP-1 production.

Journal Title

Diabetes Metab Syndr

Volume

17

Issue

12

First Page

102907

Last Page

102907

MeSH Keywords

Humans; Mice; Aged; Male; Rats; Animals; Glucagon-Like Peptide 1; Diabetes Mellitus, Type 2; L Cells; Rats, Wistar; Enteroendocrine Cells; Hepatocyte Nuclear Factor 3-alpha

Keywords

Aging; Colon; Enteroendocrine cell; Glucagon like peptide 1; High-fat and high-fructose diet

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