Zhang Tinghong, Zhu Binqiang, Deng Shijie, Qin Jinling, Zhang Jingyuan, Meng Shu
State Key Laboratory of Respiratory Disease, the First Affiliated Hospital, Guangzhou Medical University, Guangzhou, Guangdong, 510120, China.
Department of Basic Science Research, Guangzhou National Laboratory, Guangzhou, Guangdong, 510005, China.
Angiogenesis. 2025 May 2;28(3):26. doi: 10.1007/s10456-025-09979-3.
Stromal cell-derived factor-1 alpha (SDF-1α) is a promising target for therapeutic angiogenesis in ischemic diseases such as peripheral artery disease (PAD). However, the clinical application of SDF-1α protein or plasmid-based gene therapy is unsuccessful. mRNA therapy has shown great promise in protein replacement. Here, we developed DOPE-lipid nanoparticles (LNPs) encapsulating SDF-1α mRNA (LNP@SDF-1α) for efficient gene delivery. In vitro, LNP@SDF-1α treatment of human umbilical vein endothelial cells (HUVECs) significantly enhanced endothelial migration, tube formation, and increased monocyte adhesion, demonstrating robust pro-angiogenic activity. In vivo, LNP@SDF-1α transfected HUVECs showed enhanced angiogenic capacity in a murine Matrigel plug model. Furthermore, in a mouse hindlimb ischemia model, intramuscular injection of LNP@SDF-1α into ischemic limbs accelerated blood flow recovery, as assessed by laser speckle contrast imaging. Immunofluorescence staining revealed a marked increase in capillary and arteriole densities in treated tissues. Angiogenic protein profiling demonstrated an upregulation of pro-angiogenic factors, including VEGF and Ang-1, and a downregulation of anti-angiogenic factors. No significant toxicity was observed in major organs, indicating the safety of this approach. Our study demonstrates that SDF-1α mRNA therapy, delivered via DOPE-LNPs, significantly promotes vascular regeneration in ischemic tissues by enhancing angiogenesis and arteriogenesis, thereby restoring blood perfusion. This approach presents a promising therapeutic option for PAD and suggests broader applications of mRNA-based therapies for ischemic diseases.
基质细胞衍生因子-1α(SDF-1α)是诸如外周动脉疾病(PAD)等缺血性疾病中治疗性血管生成的一个有前景的靶点。然而,SDF-1α蛋白或基于质粒的基因疗法的临床应用并不成功。mRNA疗法在蛋白质替代方面已显示出巨大潜力。在此,我们开发了包裹SDF-1α mRNA的二油酰磷脂酰乙醇胺脂质纳米颗粒(LNP)(LNP@SDF-1α)用于高效基因递送。在体外,用LNP@SDF-1α处理人脐静脉内皮细胞(HUVECs)可显著增强内皮细胞迁移、管腔形成,并增加单核细胞黏附,显示出强大的促血管生成活性。在体内,LNP@SDF-1α转染的HUVECs在小鼠基质胶栓模型中显示出增强的血管生成能力。此外,在小鼠后肢缺血模型中,通过激光散斑对比成像评估,向缺血肢体肌肉注射LNP@SDF-1α可加速血流恢复。免疫荧光染色显示处理组织中的毛细血管和小动脉密度显著增加。血管生成蛋白谱分析表明促血管生成因子(包括VEGF和Ang-1)上调,抗血管生成因子下调。在主要器官中未观察到明显毒性,表明该方法的安全性。我们的研究表明,通过二油酰磷脂酰乙醇胺脂质纳米颗粒递送的SDF-1α mRNA疗法通过增强血管生成和动脉生成显著促进缺血组织中的血管再生,从而恢复血液灌注。这种方法为PAD提供了一种有前景的治疗选择,并提示基于mRNA的疗法在缺血性疾病中有更广泛的应用。