한빛사 논문
Do-Wan Kim a,1, Hye-Seon Jeong b,1, Eunseo Kim c, Hyomin Lee c, Chang-Hyung Choi b,*, Sei-Jung Lee a,*
a Department of Pharmaceutical Engineering, Daegu Haany University, Gyeongsan 38610, South Korea b Division of Cosmetic Science and Technology, Daegu Haany University, Gyeongsan 38610, South Korea c Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), Pohang 37673, South Korea
*Corresponding authors.
1These authors contributed equally to this work.
Abstract
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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