College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou 310032, China.
Cancer Center, Department of Ultrasound Medicine, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou 314408, China.
ACS Appl Bio Mater. 2024 Feb 19;7(2):1081-1094. doi: 10.1021/acsabm.3c01020. Epub 2024 Jan 31.
Hindlimb ischemia is a common disease worldwide featured by the sudden decrease in limb perfusion, which usually causes a potential threat to limb viability and even amputation or death. Revascularization has been defined as the gold-standard therapy for hindlimb ischemia. Considering that vascular injury recovery requires cellular adaptation to the hypoxia, hypoxia-inducible factor 1 α (HIF-1α) is a potential gene for tissue restoration and angiogenesis. In this manuscript, effective gene delivery vector PEI-β-CD (PC) was reported for the first application in the hindlimb ischemia treatment to deliver HIF-1α plasmid in vitro and in vivo. Our in vitro finding demonstrated that PC/HIF-1α-pDNA could be successfully entered into the cells and mediated efficient gene transfection with good biocompatibility. More importantly, under hypoxic conditions, PC/HIF-1α-pDNA could up-regulate the HUEVC cell viability. In addition, the mRNA levels of , , and were upregulated, and transcriptome results also demonstrated that the cell-related function of response to hypoxia was enhanced. The therapeutic effect of PC/HIF-1α-pDNA was further estimated in a murine acute hindlimb ischemia model, which demonstrated that intramuscular injection of PC/HIF-1α-pDNA resulted in significantly increased blood perfusion and alleviation in tissue damage, such as tissue fibrosis and inflammation. The results provide a rationale that HIF-1α-mediated gene therapy might be a practical strategy for the treatment of limb ischemia.
肢体缺血是一种常见的疾病,其特征是肢体灌注突然减少,通常会对肢体的存活能力造成潜在威胁,甚至导致截肢或死亡。再血管化被定义为治疗肢体缺血的金标准疗法。考虑到血管损伤的恢复需要细胞适应缺氧,缺氧诱导因子 1α(HIF-1α)是组织修复和血管生成的潜在基因。在本手稿中,首次报道了有效的基因传递载体 PEI-β-CD(PC)在治疗肢体缺血中的应用,以体外和体内递送 HIF-1α 质粒。我们的体外研究结果表明,PC/HIF-1α-pDNA 可以成功进入细胞,并具有良好的生物相容性,介导有效的基因转染。更重要的是,在缺氧条件下,PC/HIF-1α-pDNA 可以上调 HUEVC 细胞活力。此外,上调了 、 和 的 mRNA 水平,转录组结果也表明,细胞对缺氧的反应功能得到了增强。PC/HIF-1α-pDNA 的治疗效果在小鼠急性肢体缺血模型中进一步得到了评估,结果表明,肌肉内注射 PC/HIF-1α-pDNA 可显著增加血液灌注,并缓解组织损伤,如组织纤维化和炎症。这些结果为 HIF-1α 介导的基因治疗可能是治疗肢体缺血的一种实用策略提供了依据。