Interaction between microRNA-195 and HuR regulates Paneth cell function in the intestinal epithelium by altering SOX9 translation

Paneth cells at the bottom of small intestinal crypts secrete antimicrobial peptides, enzymes, and growth factors and contribute to pathogen clearance and maintenance of the stem cell niche. Loss of Paneth cells and their dysfunction occur commonly in various pathologies, but the mechanism underlying the control of Paneth cell function remains largely unknown. Here, we identified microRNA-195 (miR-195) as a repressor of Paneth cell development and activity by altering SOX9 translation via interaction with RNA-binding protein HuR. Tissue-specific transgenic expression of miR-195 (miR195-Tg) in the intestinal epithelium decreased the levels of mucosal SOX9 and reduced the numbers of lysozyme-positive (Paneth) cells in mice. Ectopically expressed SOX9 in the intestinal organoids derived from miR-195-Tg mice restored Paneth cell development ex vivo. miR-195 did not bind to <i>Sox9</i> mRNA but it directly interacted with HuR and prevented HuR binding to <i>Sox9</i> mRNA, thus inhibiting SOX9 translation. Intestinal mucosa from mice that harbored both <i>Sox9</i> transgene and ablation of the HuR locus exhibited lower levels of SOX9 protein and Paneth cell numbers than those observed in miR-195-Tg mice. Inhibition of miR-195 activity by its specific antagomir improved Paneth cell function in HuR-deficient intestinal organoids. These results indicate that interaction of miR-195 with HuR regulates Paneth cell function by altering SOX9 translation in the small intestinal epithelium.<b>NEW & NOTEWORTHY</b> Our results indicate that intestinal epithelial tissue-specific transgenic miR-195 expression decreases the levels of SOX9 expression, along with reduced numbers of Paneth cells. Ectopically expressed SOX9 in the intestinal organoids derived from miR-195-Tg mice restores Paneth cell development ex vivo. miR-195 inhibits SOX9 translation by preventing binding of HuR to Sox9 mRNA. These findings suggest that interaction between miR-195 and HuR controls Paneth cell function via SOX9 in the intestinal epithelium.

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Publication Details

Journal
American Journal of Physiology-Cell Physiology
Published
2024-08-05
DOI
https://doi.org/10.1152/ajpcell.00325.2024
Citations
2
Primary Topic
MicroRNA in disease regulation
Type
article
Field-Weighted Citation Impact
0.57

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article

Interaction between microRNA-195 and HuR regulates Paneth cell function in the intestinal epithelium by altering SOX9 translation

Cassandra A. Cairns, Douglas J. Turner, Ting Chen, Shweta Sharma et al.
2 citations
American Journal of Physiology-Cell Physiology
MicroRNA in disease regulation
0.57
article

Interaction between microRNA-195 and HuR regulates Paneth cell function in the intestinal epithelium by altering SOX9 translation

Cassandra A. Cairns, Douglas J. Turner, Ting Chen, Shweta Sharma, Jian‐Ying Wang, Min Seong Kwon, Tingxi Yu, Songah Chae, Hee Kyoung Chung, Lan Xiao
article en
2 citations

Abstract

Paneth cells at the bottom of small intestinal crypts secrete antimicrobial peptides, enzymes, and growth factors and contribute to pathogen clearance and maintenance of the stem cell niche. Loss of Paneth cells and their dysfunction occur commonly in various pathologies, but the mechanism underlying the control of Paneth cell function remains largely unknown. Here, we identified microRNA-195 (miR-195) as a repressor of Paneth cell development and activity by altering SOX9 translation via interaction with RNA-binding protein HuR. Tissue-specific transgenic expression of miR-195 (miR195-Tg) in the intestinal epithelium decreased the levels of mucosal SOX9 and reduced the numbers of lysozyme-positive (Paneth) cells in mice. Ectopically expressed SOX9 in the intestinal organoids derived from miR-195-Tg mice restored Paneth cell development ex vivo. miR-195 did not bind to <i>Sox9</i> mRNA but it directly interacted with HuR and prevented HuR binding to <i>Sox9</i> mRNA, thus inhibiting SOX9 translation. Intestinal mucosa from mice that harbored both <i>Sox9</i> transgene and ablation of the HuR locus exhibited lower levels of SOX9 protein and Paneth cell numbers than those observed in miR-195-Tg mice. Inhibition of miR-195 activity by its specific antagomir improved Paneth cell function in HuR-deficient intestinal organoids. These results indicate that interaction of miR-195 with HuR regulates Paneth cell function by altering SOX9 translation in the small intestinal epithelium.<b>NEW & NOTEWORTHY</b> Our results indicate that intestinal epithelial tissue-specific transgenic miR-195 expression decreases the levels of SOX9 expression, along with reduced numbers of Paneth cells. Ectopically expressed SOX9 in the intestinal organoids derived from miR-195-Tg mice restores Paneth cell development ex vivo. miR-195 inhibits SOX9 translation by preventing binding of HuR to Sox9 mRNA. These findings suggest that interaction between miR-195 and HuR controls Paneth cell function via SOX9 in the intestinal epithelium.

American Journal of Physiology-Cell PhysiologyVol. 327(3)
University of Maryland, Baltimore (US), Baltimore VA Medical Center (US)
U.S. Department of Veterans Affairs, National Institute of Diabetes and Digestive and Kidney Diseases
Openalex Percentile: Top 32%
MicroRNA in disease regulation
0.57
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