Yi Luyang, Chen Yihan, Jin Qiaofeng, Deng Cheng, Wu Ya, Li Huiling, Liu Tianshu, Li Yuman, Yang Yali, Wang Jing, Lv Qing, Zhang Li, Xie Mingxing
Department of Ultrasound, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Avenue, Wuhan, 430022, China.
Hubei Province Key Laboratory of Molecular Imaging, 13 Hangkong Road, Wuhan, 430030, China.
Adv Healthc Mater. 2020 Jul;9(14):e2000189. doi: 10.1002/adhm.202000189. Epub 2020 Jun 16.
Antagomir-155 is an artificial inhibitor of miRNA-155, which is expected to be a promising therapeutic target to attenuate acute cardiac rejection (ACR). However, its vulnerability of being degraded by endogenous nuclease and potential off-target effect make the authors seek for a more suitable way to delivery it. In attribution of efficiency and safety, ultrasound targeted microbubbles destruction (UTMD) turns out to be an appropriate method to deliver gene to target tissues. Here, cationic microbubbles to deliver antagomir-155 downregulating miRNA-155 in murine allograft hearts triggered by UTMD are synthesized. The viability of this therapy is verified by fluorescent microscopy. The biodistribution of antagomir-155 is analyzed by optical imaging system. The results show antagomir-155 delivered by UTMD which significantly decreases the levels of miR-155. Also, this therapy downregulates the expression of cytokines and inflammation infiltration. And allograft survival time is significantly prolonged. Therefore, antagomir-loaded microbubbles trigged by UTMD may provide a novel platform for ACR target treatment.
抗miR-155是一种人工合成的miRNA-155抑制剂,有望成为减轻急性心脏排斥反应(ACR)的一种有前景的治疗靶点。然而,其易被内源性核酸酶降解以及潜在的脱靶效应促使作者寻找更合适的递送方式。在效率和安全性方面,超声靶向微泡破坏(UTMD)被证明是一种将基因递送至靶组织的合适方法。在此,合成了由UTMD触发的阳离子微泡,用于递送抗miR-155,下调小鼠同种异体移植心脏中的miRNA-155。通过荧光显微镜验证了该疗法的可行性。利用光学成像系统分析了抗miR-155的生物分布。结果表明,UTMD递送的抗miR-155显著降低了miR-155的水平。此外,该疗法下调了细胞因子的表达并减轻了炎症浸润。同种异体移植心脏的存活时间显著延长。因此,UTMD触发的载抗miR-155微泡可能为ACR的靶向治疗提供一个新的平台。