microRNA-195与HuR之间的相互作用通过改变SOX9的翻译来调节肠上皮细胞的功能。

IF 5 2区 生物学 Q2 CELL BIOLOGY American journal of physiology. Cell physiology Pub Date : 2024-09-01 Epub Date: 2024-08-05 DOI:10.1152/ajpcell.00325.2024
Min S Kwon, Hee K Chung, Lan Xiao, Ting-Xi Yu, Shweta Sharma, Cassandra M Cairns, Ting Chen, Songah Chae, Douglas J Turner, Jian-Ying Wang
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引用次数: 0

摘要

小肠隐窝底部的Paneth细胞分泌抗菌肽、酶和生长因子,有助于病原体清除和干细胞龛的维持。Paneth细胞的缺失及其功能障碍通常发生在各种病症中,但Paneth细胞功能的控制机制在很大程度上仍然未知。在这里,我们发现microRNA-195(miR-195)通过与RNA结合蛋白HuR相互作用改变SOX9的翻译,从而抑制Paneth细胞的发育和活性。在小鼠肠上皮细胞中组织特异性转基因表达 miR-195(miR195-Tg)会降低粘膜 SOX9 的水平,并减少溶菌酶阳性(Paneth)细胞的数量。miR-195不与Sox9 mRNA结合,但它直接与HuR相互作用,阻止HuR与Sox9 mRNA结合,从而抑制了SOX9的翻译。同时携带 Sox9 转基因和消减 HuR 基因座的小鼠肠粘膜的 SOX9 蛋白水平和 Paneth 细胞数量低于 miR-195-Tg 小鼠。用特异性抗凝血酶抑制 miR-195 的活性可改善 HuR 缺失肠器官组织中 Paneth 细胞的功能。这些结果表明,miR-195 与 HuR 的相互作用通过改变小肠上皮细胞中 SOX9 的翻译来调节 Paneth 细胞的功能。
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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 Sox9 mRNA but it directly interacted with HuR and prevented HuR binding to Sox9 mRNA, thus inhibiting SOX9 translation. Intestinal mucosa from mice that harbored both Sox9 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.NEW & NOTEWORTHY 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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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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