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高脂肪喂养引起的脱氧胆酸水平升高通过减少回肠中的 IL-22 来损伤肠道干细胞。

An elevated deoxycholic acid level induced by high-fat feeding damages intestinal stem cells by reducing the ileal IL-22.

机构信息

Department of Gastroenterology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; Shanghai Key Laboratory of Pancreatic Diseases, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Digestive Endoscopic Center, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

出版信息

Biochem Biophys Res Commun. 2021 Nov 19;579:153-160. doi: 10.1016/j.bbrc.2021.09.061. Epub 2021 Sep 25.

Abstract

Long-term high-fat diet (HFD) destroys the intestinal mucosal barrier by damaging intestinal stem cells (ISCs). A HFD can increase the concentration of intestinal deoxycholic acid (DCA) and decrease the secretion of interleukin-22 (IL-22), which plays an important role in the proliferation, repair and regeneration of ISCs. We hypothesized that increased level of intestinal DCA induced by a HFD leads to ISC dysfunction by reducing the IL-22 levels in intestinal tissues. In this study, 2 weeks of a DCA diet or a HFD damaged ileal ISC and its proliferation and differentiation, resulting in a decrease in Paneth cells and goblet cells. Importantly, 2 weeks of a DCA diet or a HFD also reduced ileal IL-22 concentration, accompanied by a decreased number of group 3 innate lymphoid cells in ileal mucosa, which produce IL-22 after intestinal injury. Concurrent feeding with bile acid binder cholestyramine prevented all these changes induced by a HFD. In addition, in vitro study further confirmed that exogenous IL-22 reversed the decline in the proliferation and differentiation of ileal ISCs induced by DCA stimulation. Collectively, these results revealed that the decrease in intestinal IL-22 induced by DCA may be a novel mechanism by which HFD damages ISCs. The administration of IL-22 or a bile acid binder may provide novel therapeutic targets for the metabolic syndrome caused by a HFD.

摘要

长期高脂肪饮食(HFD)通过破坏肠干细胞(ISCs)来破坏肠道黏膜屏障。HFD 可以增加肠道脱氧胆酸(DCA)的浓度并减少白细胞介素-22(IL-22)的分泌,IL-22 在 ISCs 的增殖、修复和再生中起着重要作用。我们假设 HFD 引起的肠道 DCA 水平升高通过降低肠道组织中的 IL-22 水平导致 ISC 功能障碍。在这项研究中,2 周的 DCA 饮食或 HFD 损伤回肠 ISC 及其增殖和分化,导致潘氏细胞和杯状细胞减少。重要的是,2 周的 DCA 饮食或 HFD 还降低了回肠 IL-22 浓度,同时回肠黏膜中产生 IL-22 的第 3 组固有淋巴细胞数量减少,这些细胞在肠道损伤后产生 IL-22。同时给予胆汁酸结合剂考来烯胺可预防 HFD 引起的所有这些变化。此外,体外研究进一步证实,外源性 IL-22 逆转了 DCA 刺激引起的回肠 ISC 增殖和分化下降。总之,这些结果表明,DCA 诱导的肠道 IL-22 减少可能是 HFD 损伤 ISC 的一种新机制。IL-22 或胆汁酸结合剂的给药可能为 HFD 引起的代谢综合征提供新的治疗靶点。

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