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Exosomes from mesenchymal stromal cells reduce murine colonic inflammation via a macrophage-dependent mechanism
Huashan Liu, Zhenxing Liang, Fengwei Wang, Chi Zhou, Xiaobin Zheng, Tuo Hu, Xiaowen He, Xianrui Wu, Ping Lan
Huashan Liu, Zhenxing Liang, Fengwei Wang, Chi Zhou, Xiaobin Zheng, Tuo Hu, Xiaowen He, Xianrui Wu, Ping Lan
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Research Article Stem cells Therapeutics

Exosomes from mesenchymal stromal cells reduce murine colonic inflammation via a macrophage-dependent mechanism

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Abstract

Conventional treatments for inflammatory bowel disease (IBD) have multiple potential side effects. Therefore, alternative treatments are desperately needed. This work demonstrated that systemic administration of exosomes from human bone marrow–derived mesenchymal stromal cells (MSC-Exos) substantially mitigated colitis in various models of IBD. MSC-Exos treatment downregulated inflammatory responses, maintained intestinal barrier integrity, and polarized M2b macrophages but did not favor intestinal fibrosis. Mechanistically, infused MSC-Exos acted mainly on colonic macrophages, and macrophages from colitic colons acquired obvious resistance to inflammatory restimulation when prepared from mice treated with MSC-Exos versus untreated mice. The beneficial effect of MSC-Exos was blocked by macrophage depletion. Also, the induction of IL-10 production from macrophages was partially involved in the beneficial effect of MSC-Exos. MSC-Exos were enriched in proteins involved in regulating multiple biological processes associated with the anticolitic benefit of MSC-Exos. Particularly, metallothionein-2 in MSC-Exos was required for the suppression of inflammatory responses. Taken together, MSC-Exos are critical regulators of inflammatory responses and may be promising candidates for IBD treatment.

Authors

Huashan Liu, Zhenxing Liang, Fengwei Wang, Chi Zhou, Xiaobin Zheng, Tuo Hu, Xiaowen He, Xianrui Wu, Ping Lan

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Figure 1

Characterization of MSC-Exos.

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Characterization of MSC-Exos.
Three independent experiments were perform...
Three independent experiments were performed and yielded similar results. (A) Flow cytometry analysis showing the phenotypic markers of passage 5 MSCs cultured in medium supplemented with 10% exosome-depleted fetal bovine serum (FBS). Numerical values denote the percentage of positive cells. (B) Flow cytometry analysis for PI and Annexin V of MSCs cultured in exosome-depleted FBS medium. The apoptosis of MSCs was induced by 10 μM etoposide as a positive control. Numerical values denote the percentage of apoptotic cells (Annexin V+). (C) Size profile of MSC-Exos by PMX. (D) TEM analysis of MSC-Exos. TEM using negative staining with uranyl acetate (left) and tungstophosphoric acid (right). Scale bars: 200 nm (left), 50 nm (right). (E) Western blot analysis of TSG101 and CD9. Extracts of MSC-Exos were exposed to Triton X-100 plus proteinase K (PK) or PK alone. MW, molecular weight.

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