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人乳寡糖通过激活肠道细胞分化预防坏死性小肠结肠炎。

Human Milk Oligosaccharides Protect against Necrotizing Enterocolitis by Activating Intestinal Cell Differentiation.

机构信息

Translational Medicine Program, The Hospital for Sick Children, Toronto, M5G 1X8, Canada.

Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, M5G 1X8, Canada.

出版信息

Mol Nutr Food Res. 2020 Nov;64(21):e2000519. doi: 10.1002/mnfr.202000519. Epub 2020 Oct 4.

Abstract

SCOPE

Necrotizing enterocolitis (NEC) is a devastating gastrointestinal emergency and currently the leading cause of mortality in preterm infants. Recent studies show that human milk oligosaccharides (HMOs) reduce the frequency and incidence of NEC; however, the molecular mechanisms for their protection are largely unexplored.

METHODS AND RESULTS

To address this gap, a genome-wide profiling of the intestinal epithelial transcriptome in response to HMOs using RNA-sequencing is performed. It is found that HMOs alter the host transcriptome in 225 unique target genes pertaining to cell proliferation and differentiation, including upregulation of stem cell differentiation marker HMGCS2. To validate these results, differentiation in Caco-2Bbe1 (Caco-2) intestinal cells is verified by Alcian Blue staining and transepithelial electrical resistance (TER) recordings. Furthermore, an in vivo model of NEC is also employed whereby neonatal pups are gavage fed HMOs. Interestingly, HMOs-fed pups show enhanced cell MUC2 differentiation and HMGCS2 expression.

CONCLUSIONS

These findings demonstrate HMOs protect against NEC in part by altering the differentiation of the crypt-villus axis. In addition, this study suggests that pooled HMOs directly induce a series of biological processes, which provide mechanistic insights to how HMOs protect the host intestine.

摘要

范围

坏死性小肠结肠炎(NEC)是一种严重的胃肠道急症,也是目前早产儿死亡的主要原因。最近的研究表明,人乳寡糖(HMOs)可降低 NEC 的发生频率和发病率;然而,其保护作用的分子机制在很大程度上仍未被探索。

方法和结果

为了解决这一差距,我们使用 RNA 测序对 HMOs 作用于肠道上皮转录组进行了全基因组分析。结果发现,HMOs 改变了 225 个与细胞增殖和分化相关的宿主转录本,包括上调干细胞分化标志物 HMGCS2。为了验证这些结果,通过阿尔辛蓝染色和跨上皮电阻(TER)记录验证了 Caco-2Bbe1(Caco-2)肠细胞的分化。此外,还采用了 NEC 的体内模型,即用 HMOs 对新生幼鼠进行灌胃。有趣的是,HMOs 喂养的幼鼠显示出细胞 MUC2 分化和 HMGCS2 表达增强。

结论

这些发现表明,HMOs 通过改变隐窝-绒毛轴的分化来部分保护 NEC。此外,本研究表明,混合 HMOs 可直接诱导一系列生物学过程,为 HMOs 如何保护宿主肠道提供了机制见解。

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