Oral delivery of stem-cell-loaded hydrogel microcapsules restores gut inflammation and microbiota

干细胞 间充质干细胞 罗伊乳杆菌 失调 益生菌 化学 肠道菌群 微生物学 免疫学 生物 乳酸菌 细胞生物学 生物化学 细菌 遗传学 发酵
作者
Do Wan Kim,Hye‐Seon Jeong,Eunseo Kim,Hyomin Lee,Chang‐Hyung Choi,Sei‐Jung Lee
出处
期刊:Journal of Controlled Release [Elsevier BV]
卷期号:347: 508-520 被引量:30
标识
DOI:10.1016/j.jconrel.2022.05.028
摘要

Mesenchymal stem cells (MSCs) are an attractive candidate for the treatment of inflammatory bowel disease (IBD), but their poor delivery rate to an inflamed colon is a major factor hampering the clinical potential of stem cell therapies. Moreover, there remains a formidable hurdle to overcome with regard to survival and homing in to injured sites. Here, we develop a strategy utilizing monodisperse hydrogel microcapsules with a thin intermediate oil layer prepared by a triple-emulsion drop-based microfluidic approach as an in-situ oral delivering carrier. The oral delivery of stem-cell-loaded hydrogel microcapsules (SC-HM) enhances MSC survival and retention in the hostile stomach environment due to the intermediate oil layer and low value of the overall stiffness, facilitating programmable cell release during gastrointestinal peristalsis. SC-HM is shown to induce tissue repair, reduce the colonic macrophage infiltration responsible for the secretion of the pro-inflammatory factors, and significantly mitigate the severity of IBD in a mouse model, where MSCs released by SC-HM successfully accumulate at the colonic crypt. Moreover, a metagenomics analysis reveals that SC-HM ameliorates the dysbiosis of specific bacterial genera, including Bacteroides acidifaciens, Lactobacillus (L.) gasseri, Lactobacillus reuteri, and L. intestinalis, implying optimization of the microorganism's composition and abundance. These findings demonstrate that SC-HM is a potential IBD treatment candidate.
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