Anti-apoptotic cardioprotective effects of SHP-1 gene silencing against ischemiaareperfusion injury: Use of deoxycholic acid-modified low molecular weight polyethyleneimine as a cardiac siRNA-carrier

• Published in: Journal of controlled release 2013-06, Vol.168 (2), p.125-134
• Main Authors: Kim, Dongkyu, Hong, Jueun, Moon, Hyung-Ho, Nam, Hye, Mok, Hyejung, Jeong, Ji, Kim, Sung, Choi, Donghoon, Kim, Sun
• Format: Article
• Language: English
• Subjects: Apoptosis
• ISSN: 0168-3659
• DOI: 10.1016/j.jconrel.2013.02.031

The cardiomyocyte apoptosis plays a critical role in the development of myocardial injury after ischemia and reperfusion. Thus, alteration of the major apoptosis-regulatory factors during myocardial ischemiaareperfusion is expected to have favorable cardioprotective effects. Herein, we report ischemicareperfused myocardial infarction (MI) repair with siRNA against Src homology region 2 domain-containing tyrosine phosphatase-1 (SHP-1), which is known as a key factor involved in regulating the progress of apoptosis in many cell types. A low molecular weight polyethyleneimine modified with deoxycholic acid (PEI1.8aDA)-based delivery strategy was suggested for the cardiac application of SHP-1 siRNA to overcome the poor gene delivery efficiency to myocardium due to the highly charged structures of the compact cardiac muscles. The PEI1.8aDA conjugates formed stable nanocomplexes with SHP-1 siRNA via electrostatic and hydrophobic interactions. The PEI1.8aDA/SHP-1 siRNA polyplexes effectively silenced SHP-1 gene expression in cardiomyocytes, leading to a significant inhibition of cardiomyocyte apoptosis under hypoxia. In comparison to conventional gene carriers, relatively large amounts of siRNA molecules remained after treatment with the PEI1.8aDA/SHP-1 siRNA polyplexes. Cardiac administration of the PEI1.8aDA/SHP-1 siRNA polyplexes resulted in substantial improvement in SHP-1 gene silencing, which can be explained by the enhancement of cardiac delivery efficiency of the PEI1.8aDA conjugates. In addition, in vivo treatment with the PEI1.8aDA/SHP-1 siRNA polyplexes induced a highly significant reduction in myocardial apoptosis and infarct size in rat MI models. These results demonstrate that the PEI1.8aDA/SHP-1 siRNA polyplex formulation is a useful system for efficient gene delivery into the compact myocardium that provides a fundamental advantage in treating ischemicareperfused MI.