Suppr超能文献

锌-L-天冬氨酸通过激活 Wnt/β-连环蛋白信号通路增强肠干细胞活性,以保护肠黏膜免受脱氧雪腐镰刀菌烯醇的损伤。

Zinc L-Aspartate enhances intestinal stem cell activity to protect the integrity of the intestinal mucosa against deoxynivalenol through activation of the Wnt/β-catenin signaling pathway.

机构信息

College of Animal Science, South China Agricultural University, Guangdong Laboratory of Lingnan Modern Agriculture, Guangdong Provincial Key Laboratory of Animal Nutrition Control, National Engineering Research Center for Breeding Swine Industry, Guangzhou, Guangdong, China.

College of Letters & Science, University of Wisconsin-Madison, Madison, WI, United States.

出版信息

Environ Pollut. 2020 Jul;262:114290. doi: 10.1016/j.envpol.2020.114290. Epub 2020 Mar 3.

Abstract

The micronutrient, zinc, plays a vital role in modulating cellular signaling recognition and enhancing intestinal barrier function. However, the precise mechanisms underlying the zinc regulation of intestinal stem cell (ISC) renewal and regeneration ability, which drive intestinal epithelial turnover to maintain the intestinal barrier, under physiological and pathological conditions are unknown. In this study, we used in vivo mouse plus ex vivo enteroid model to investigate thoroughly the protection efficacy of zinc L-aspartate (Zn-Asp) on intestinal mucosal integrity exposed to deoxynivalenol (DON). The results showed that 10 rather than 20 mg/kg body weight (BW) Zn-Asp (calculation in zinc) significantly increased the jejunum mass and ameliorated mucosa injury caused by 2 mg/kg BW DON treatment, including improvement of the intestinal morphology and barrier, as well as enteroid-forming and -budding efficiency, which was expanded from crypt cells isolated from jejunum of mice in each group. The repair process stimulated by Zn-Asp was also accompanied by increased fluorescence signal intensity of KRT20 and Villin; increased numbers of MUC2, CAG, LYZ, BrdU and Ki67 cells in mouse jejunum; and protein expression of Ki67 and PCNA in the jejunum, crypt and enteroid. Simultaneously, Zn-Asp increased ISC activity to promote intestinal epithelial renewal even under physiological conditions. These results were further verified in ex vivo enteroid culture experiments, which were treated with 100 μmol/L Zn-Asp (calculation in zinc) and 100 ng/mL DON for 72 h. Furthermore, we demonstrated that Zn-Asp improved intestinal integrity or accelerated wound healing along with Wnt/β-catenin signaling upregulation or reactivation. Our findings indicate Zn-Asp, especially Zn, enhances ISC activity to maintain the intestinal integrity by activating the Wnt/β-catenin signaling, which sheds some light upon effective preventive strategies for intestinal injury induced by mycotoxin based on ISCs with exogenous zinc preparations in the proper drugs, health foods or qualified feed.

摘要

微量元素锌在调节细胞信号识别和增强肠道屏障功能方面起着至关重要的作用。然而,在生理和病理条件下,锌调节肠道干细胞(ISC)更新和再生能力的精确机制,以及驱动肠道上皮细胞更替以维持肠道屏障的机制尚不清楚。在这项研究中,我们使用体内小鼠加体外类器官模型,深入研究了锌 L-天冬氨酸(Zn-Asp)对暴露于脱氧雪腐镰刀菌烯醇(DON)的肠道黏膜完整性的保护作用。结果表明,10mg/kg 体重(BW)而不是 20mg/kg BW 的 Zn-Asp(按锌计算)显著增加了空肠质量,并改善了 2mg/kg BW DON 处理引起的黏膜损伤,包括改善了肠道形态和屏障,以及类器官的形成和出芽效率,这是从每组小鼠空肠分离的隐窝细胞中扩大而来的。Zn-Asp 刺激的修复过程还伴随着 KRT20 和 Villin 的荧光信号强度增加;小鼠空肠中 MUC2、CAG、LYZ、BrdU 和 Ki67 细胞数量增加;以及 jejunum、crypt 和 enteroid 中的 Ki67 和 PCNA 蛋白表达增加。同时,Zn-Asp 增加了 ISC 活性,即使在生理条件下也能促进肠道上皮细胞更新。这些结果在体外类器官培养实验中得到了进一步验证,该实验用 100μmol/L Zn-Asp(按锌计算)和 100ng/mL DON 处理 72h。此外,我们证明了 Zn-Asp 通过上调或重新激活 Wnt/β-catenin 信号,改善了肠道完整性或加速了伤口愈合。我们的研究结果表明,Zn-Asp 通过激活 Wnt/β-catenin 信号增强 ISC 活性来维持肠道完整性,这为基于 ISC 的真菌毒素诱导的肠道损伤提供了一些有效的预防策略,这些策略可以通过外源性锌制剂在适当的药物、保健品或合格饲料中实现。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验