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miR-10a-5p和miR-10b-5p可恢复老年小鼠的结肠运动能力。

miR-10a-5p and miR-10b-5p restore colonic motility in aged mice.

作者信息

Baek Gain, Singh Rajan, Ha Se Eun, Cho Hayeong, Padmanabhan Sesh, Vishwanath Vachan, Kim Min Seob, Seon Dahyun, You Jisong, Lee Moon Young, Ro Seungil

机构信息

Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, United States.

Department of Physiology, Wonkwang University, Iksan 54538, South Korea.

出版信息

World J Gastroenterol. 2025 Jun 28;31(24):104437. doi: 10.3748/wjg.v31.i24.104437.

Abstract

BACKGROUND

We previously identified miR-10b-5p as a key regulator of gastrointestinal (GI) motility through its essential role in the development and function of interstitial cells of Cajal (ICC), the pacemaker cells of the gut. Loss of miR-10b-5p in ICC impairs intestinal motility and contributes to constipation, a common condition in the elderly. Notably, miR-10b-5p is co-expressed with its paralog, miR-10a-5p, in ICC.

AIM

To investigate the roles of miR-10a-5p and miR-10b-5p in age-associated intestinal dysmotility and assess the therapeutic potential of restoring their expression.

METHODS

We employed aged mice, and single and double knockout (KO) models, and human plasma and colon samples across age groups. GI and colonic transit, ICC network integrity, and expression levels of miR-10a/b-5p were evaluated. Additionally, we tested whether treatment with their microRNA mimics could restore GI motility in aged mice.

RESULTS

Aged mice exhibited delayed GI and colonic transit, reduced fecal output, and diminished expression of miR-10a-5p and miR-10b-5p, which peaked during late embryonic and early postnatal stages and declined with age. This decline paralleled ICC network deterioration in the colon. All KO models exhibited impaired motility and ICC loss, with KO mice displaying more severe phenotypes than KO mice. Double KO mice demonstrated growth retardation and reduced survival, with homozygous mutants living only up to 3 months. Treatment of aged mice with miR-10a-5p and miR-10b-5p mimics encapsulated in jetPEI significantly improved GI and colonic motility. Successful delivery to the gut, including the colon, was confirmed. In human samples, both miR-10a/b-5p and KIT expression decreased with age.

CONCLUSION

miR-10a-5p and miR-10b-5p are essential for ICC maintenance and colonic motility, and their age-related decline contributes to GI dysmotility in both mice and humans. Restoring their levels offers a promising therapeutic strategy for treating age-related constipation and other motility disorders.

摘要

背景

我们之前已确定miR-10b-5p是胃肠(GI)动力的关键调节因子,其在肠道起搏细胞即 Cajal间质细胞(ICC)的发育和功能中发挥重要作用。ICC中miR-10b-5p的缺失会损害肠道动力并导致便秘,这在老年人中是一种常见病症。值得注意的是,miR-10b-5p与其旁系同源物miR-10a-5p在ICC中共表达。

目的

研究miR-10a-5p和miR-10b-5p在年龄相关的肠道动力障碍中的作用,并评估恢复其表达的治疗潜力。

方法

我们使用了老年小鼠、单基因和双基因敲除(KO)模型,以及不同年龄组的人类血浆和结肠样本。评估了胃肠和结肠转运、ICC网络完整性以及miR-10a/b-5p的表达水平。此外,我们测试了用它们的微小RNA模拟物进行治疗是否能恢复老年小鼠的胃肠动力。

结果

老年小鼠表现出胃肠和结肠转运延迟、粪便排出量减少,以及miR-10a-5p和miR-10b-5p表达降低,这两种微小RNA在胚胎后期和出生后早期达到峰值,并随年龄增长而下降。这种下降与结肠中ICC网络的恶化平行。所有KO模型均表现出动力受损和ICC丢失,单基因敲除小鼠的表型比双基因敲除小鼠更严重。双基因敲除小鼠表现出生长发育迟缓且存活率降低,纯合突变体仅存活至3个月。用jetPEI包裹的miR-10a-5p和miR-10b-5p模拟物治疗老年小鼠可显著改善胃肠和结肠动力。证实了其成功递送至包括结肠在内的肠道。在人类样本中,miR-10a/b-5p和KIT的表达均随年龄增长而降低。

结论

miR-10a-5p和miR-10b-5p对ICC维持和结肠动力至关重要,它们与年龄相关的下降导致小鼠和人类的胃肠动力障碍。恢复它们的水平为治疗年龄相关便秘和其他动力障碍提供了一种有前景的治疗策略。

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