Qiu C, Peng W K, Shi F, Zhang T
Department of Respiratory Diseases, Second Clinical Medical College, Jinan University, Shenzhen, Guangdong, P.R. China.
Genet Mol Res. 2012 Sep 13;11(3):3236-45. doi: 10.4238/2012.September.12.6.
Activation of the transcription factor signal transducer and activator of transcription 5b (STAT5b) is a key event in the development of asthma. The potent ability of small interfering RNA (siRNA) to inhibit the expression of STAT5b mRNA has provided a new class of therapeutics for asthma. However, efficient delivery of siRNAs remains a key obstacle to their successful application. A targeted intracellular delivery approach for siRNA to specific cell types would be highly desirable. We used packaging RNA (pRNA), a component of the bacteriophage phi29-packaging motor, to deliver STAT5b siRNA to asthmatic spleen lymphocytes. This pRNA was able to spontaneously carry siRNA/STAT5b and aptamer/CD4, which is a ligand to CD4 molecule. Based on RT-PCR data, the pRNA dimer effectively inhibited STAT5b gene mRNA expression of asthmatic spleen lymphocytes, without the need for additional transfections. We conclude that the pRNA dimer carrying both siRNA and aptamer can deliver functional siRNA to cells; possibly, the aptamer acts as a ligand to interact with specific receptors. The pRNAs were evaluated with a CCK-8 kit and were found to have little cytotoxicity. We conclude that pRNA as a novel nanovehicle for RNA worth further study.
转录因子信号转导子和转录激活子5b(STAT5b)的激活是哮喘发展过程中的关键事件。小干扰RNA(siRNA)抑制STAT5b mRNA表达的强大能力为哮喘提供了一类新的治疗方法。然而,siRNA的有效递送仍然是其成功应用的关键障碍。将siRNA靶向细胞内递送至特定细胞类型的方法将是非常理想的。我们使用包装RNA(pRNA),即噬菌体phi29包装马达的一个组成部分,将STAT5b siRNA递送至哮喘患者的脾脏淋巴细胞。这种pRNA能够自发携带siRNA/STAT5b和适体/CD4(CD4分子的一种配体)。基于逆转录聚合酶链反应(RT-PCR)数据,pRNA二聚体有效地抑制了哮喘患者脾脏淋巴细胞中STAT5b基因mRNA的表达,无需额外转染。我们得出结论,携带siRNA和适体的pRNA二聚体可以将功能性siRNA递送至细胞;可能的是,适体作为一种配体与特定受体相互作用。用CCK-8试剂盒对pRNA进行评估,发现其细胞毒性很小。我们得出结论,pRNA作为一种新型的RNA纳米载体值得进一步研究。