Exosomes derived from mesenchymal stem cells containing berberine for ulcerative colitis therapy

被引:10
作者
Deng, Chao [1 ]
Zhang, Huanxiao [1 ]
Li, Yuxuan [1 ]
Cheng, Xinyi [1 ]
Liu, Youyi [1 ]
Huang, Shubing [1 ]
Cheng, Jianqing [1 ]
Chen, Hui [2 ]
Shao, Ping [2 ]
Jiang, Bing [2 ]
Wang, Xianwen [3 ]
Wang, Kewei [4 ]
机构
[1] Jiangnan Univ, Wuxi Sch Med, Wuxi 214122, Peoples R China
[2] Yixing Hosp Tradit Chinese Med, Wuxi 214200, Peoples R China
[3] Anhui Med Univ, Res & Engn Ctr Biomed Mat, Sch Biomed Engn, Hefei 230032, Peoples R China
[4] Jiangnan Univ, Affiliated Hosp, Wuxi 214122, Peoples R China
关键词
Ulcerative colitis therapy; Exosomes; Berberine; Anti-inflammatory activity; DRUG-DELIVERY; EPIDEMIOLOGY; ANGIOGENESIS; INFLAMMATION; DERIVATIVES;
D O I
10.1016/j.jcis.2024.05.162
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Berberine (Ber), an isoquinoline alkaloid, is a potential drug therapy for ulcerative colitis (UC) because of its antiinflammatory activity, high biological safety, and few side effects. Nevertheless, its clinical application is hindered by its limited water solubility and low bioavailability. Currently, compared to synthetic nanocarriers, exosomes as carriers possess advantages such as low toxicity, high stability, and high specificity. Human placental mesenchymal stem cell -derived exosomes (HplMSC-Exos) have emerged as a promising drug delivery system, offering intrinsic anti-inflammatory and antioxidant activities. Therefore, we engineered MSC-Exos loaded with Ber (Exos-Ber) to enhance the solubility and bioavailability of Ber and for colon targeting, revealing a novel approach for treating UC with natural compounds. Structurally and functionally, Exos-Ber closely resembled unmodified Exos. Both in vitro and in vivo investigations confirmed the antioxidant and anti-inflammatory properties of Exos-Ber. Notably, Exos-Ber exhibited reparative effects on injured epithelial cells and reduced cellular apoptosis. Furthermore, Exos-Ber concurrently demonstrated anti-inflammatory and antioxidant activities, contributing to the mitigation of UC, possibly through its modulation of the MAPK signaling pathway. Overall, our findings demonstrate the potential of Exos-Ber as a promising therapeutic option for alleviating UC, highlighting its capacity to enhance the clinical applicability of Ber.
引用
收藏
页码:354 / 373
页数:20
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