miR-181a-5p mediates the effects of BMP4 on intestinal cell proliferation and differentiation

Chang Li, Yuning Zhou, Zhijie Yin, Yinping Jiang, Jinpeng Liu, Heidi L. Weiss, Qingding Wang, B. Mark Evers

Research output: Contribution to journalArticlepeer-review

Abstract

The intestinal mucosa undergoes a dynamic process of continual proliferation, differentiation, and apoptosis. Delineating the mechanisms involved in intestinal epithelial cell (IEC) differentiation is crucial to our understanding of not only normal gut adaptation but also aberrant intestinal growth. Bone morphogenetic protein (BMP) signaling is a pivotal regulator of intestinal proliferation and differentiation. However, the molecular underpinnings of the BMP pathway in this context are not entirely known. Here, we show a key role for the BMP4/microRNA (miR)-181/glycolysis signaling pathway in the maintenance of intestinal epithelial cell proliferation and differentiation. Treatment with BMP4 increased the expression of enterocyte markers and decreased proliferation of IECs, and importantly, decreased the expression of miR-181a-5p in mouse and human intestinal organoids. miR-181a-5p is a member of the miR-181 family with the highest expression in IECs. Treatment with locked nucleic acid (LNA) miR-181a-5p inhibitor significantly increased enterocyte differentiation as noted by increased expression of enterocyte markers in human and mouse intestinal organoids. In addition, LNA miR-181a-5p inhibitor repressed intestinal stem cell self-renewal as noted by the decreased organoid forming efficiency and expression of Ki67, cyclin D1, OLFM4 in human and mouse intestinal organoids. Moreover, in vivo administration of LNA miR-181a-5p inhibitor enhanced increased intestinal enterocyte differentiation and repressed intestinal cell proliferation. In contrast, overexpression of miR-181a-5p mimic decreased basal and BMP4-induced expression of enterocyte markers. Moreover, BMP4 treatment or inhibition of miR-181a-5p repressed hexokinase (HK) 1 expression and inhibited glycolysis. Consistently, knockdown of HK1 or inhibition of glycolysis using 2-deoxyglucose (2-DG) promoted enterocyte maturation and inhibited proliferation of IECs. Together, we provide evidence showing that miR-181a-5p inhibits intestinal enterocyte differentiation and promotes IEC proliferation through HK1-dependent glycolysis. Importantly, our findings identify miR-181a-5p as downstream in mediating BMP4 induction of enterocyte differentiation and inhibition of proliferation in IECs.

Original languageEnglish
Article number420
JournalCell Death and Disease
Volume16
Issue number1
DOIs
StatePublished - Dec 2025

Bibliographical note

Publisher Copyright:
© The Author(s) 2025.

Funding

The authors thank the Markey Cancer Center Research Communications Office for manuscript preparation; the Biospecimen Procurement and Translational Pathology Shared Resource (SR), the Redox Metabolism SR, and the Biostatistics and Bioinformatics SR of the University of Kentucky Markey Cancer Center (supported by National Cancer Institute grant P30 CA177558 to BME). This work was supported by National Institutes of Health grants R01 DK048498 (BME) and R01 CA272669 (QW and BME).

FundersFunder number
University of Kentucky Markey Cancer Center
Redox Metabolism
Markey Cancer Center Research Communications Office
National Childhood Cancer Registry – National Cancer InstituteP30 CA177558
National Childhood Cancer Registry – National Cancer Institute
National Institutes of Health (NIH)R01 DK048498, R01 CA272669
National Institutes of Health (NIH)

    ASJC Scopus subject areas

    • Immunology
    • Cellular and Molecular Neuroscience
    • Cell Biology
    • Cancer Research

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