Delivery of microRNA-1 inhibitor by dendrimer-based nanovector: An early targeting therapy for myocardial infarction in mice

作者：Xue, Xiaomei; Shi, Xueyin; Dong, Haiqing; You, Shasha; Cao, Huimin; Wang, Kun; Wen, Ya; Shi, Donglu; He, Bin^*; Li, Yongyong^*

来源：Nanomedicine: Nanotechnology, Biology and Medicine , 2018, 14(2): 619-631.

DOI：10.1016/j.nano.2017.12.004

• Early targeting therapy
• Nanovector
• Dendrigraft poly-L-lysine
• miRNA-1
• Myocardial infarction

Myocardial infarction (MI), known to be rapidly progressed and fatal, necessitates a timely and effective intervention particularly within golden 24 h. The crux is to develop a therapeutic agent that can early target the infarct site with integrated therapeutic capacity. Finding the AT(1) receptor being most over-expressed at 24 h after MI, we developed a nanovector (AT(1)-PEG-DGL) anchored with AT(1) targeting peptide, and simultaneously armed it with specific microRNA-1 inhibitor (AMO-1) to attenuate cardiomyocyte apoptosis. In vivo imaging after IV administration demonstrated that AT(1)-PEG-DGL quickly accumulated in the MI heart during the desired early period, significantly outperforming the control group without AT(1) targeting. Most importantly, a pronounced in-vivo anti-apoptosis effect was observed upon a single IV injection. Apoptotic cell death in the infarct border zone was significantly decreased and the myocardial infarct size was reduced by 64.1% as compared with that in MI control group, promising for early MI treatment.

• 出版日期2018-2
• 单位上海交通大学; 同济大学