Song Yuwen, Xu Tingting, Li Hao, Liu Jing, Cao Shumin, Yang Yichen, Li Nianlu, Lv Peiwen, Han Min, Sun Haohan, Dang Guangfu, Li Jianxin, Sun Hao, Xin Tao, Xia Huitang, Zhang Canwei
Department of Ophthalmology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan 250014, Shandong, China; Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250000, Shandong, China.
College of Biological Science and Medical Engineering, Donghua University, Shanghai 201620, China.
J Control Release. 2025 Jul 10;383:113811. doi: 10.1016/j.jconrel.2025.113811. Epub 2025 May 3.
Corneal neovascularization (CoNV) is a leading cause of visual impairment worldwide. However, CoNV remains challenging to cure clinically because of the limitations of current drugs. New and more effective therapeutic formulations for CoNV treatment are therefore urgently needed. Antisense oligonucleotide drugs hold great promise for the treatment of neovascular diseases, and ionizable cationic lipid nanoparticles (icLNPs) have shown excellent performance for nucleic acid delivery, with high encapsulation, good cellular uptake, and effective endosomal escape. In the present study, we identified integrin β1 (Itgb1) as a key gene involved in angiogenesis and revealed the significant upregulation of Flt1 in vascular endothelial cells and pericytes in CoNV using single-cell sequencing. Itgb1 knockdown significantly inhibited the proliferation and migration of vascular endothelial cells and CoNV in mice. Based on these findings, we developed Itgb1-small interfering RNA (siRNA)-loaded icLNPs, and conjugated anti-Flt1 peptide to their surface to improve CoNV targeting. Furthermore, because lipid nanoparticles reportedly trigger immune responses by upregulating pro-inflammatory cytokine expression, which may promote neovascularization, we modified triptolide (a compound with anti-inflammatory properties) into the icLNPs. The triptolide-modified, anti-Flt1 peptide-conjugated, and Itgb1-siRNA-loaded icLNPs (Itgb1-siRNA@TPL) effectively inhibited the proliferation and migration of vascular endothelial cells in vitro and CoNV in mice after eye drop administration. These effects occurred via downregulation of the PI3K/AKT and NF-κB signaling pathways. Finally, the biosafety of Itgb1-siRNA@TPL was tested, and the results revealed that it was not toxic to the cornea or major organs and had no impact on corneal epithelial healing. In conclusion, Itgb1-siRNA@TPL represent a novel, noninvasive, and effective approach for the treatment of CoNV.
角膜新生血管化(CoNV)是全球视力损害的主要原因。然而,由于现有药物的局限性,CoNV的临床治疗仍然具有挑战性。因此,迫切需要新的、更有效的治疗CoNV的制剂。反义寡核苷酸药物在治疗新生血管疾病方面具有巨大潜力,而可电离阳离子脂质纳米颗粒(icLNPs)在核酸递送方面表现出色,具有高封装率、良好的细胞摄取和有效的内体逃逸能力。在本研究中,我们确定整合素β1(Itgb1)是参与血管生成的关键基因,并通过单细胞测序揭示了CoNV中血管内皮细胞和周细胞中Flt1的显著上调。敲低Itgb1可显著抑制小鼠血管内皮细胞的增殖和迁移以及CoNV的形成。基于这些发现,我们开发了负载Itgb1小干扰RNA(siRNA)的icLNPs,并在其表面偶联抗Flt1肽以改善对CoNV的靶向作用。此外,据报道脂质纳米颗粒会通过上调促炎细胞因子表达引发免疫反应,这可能促进新生血管形成,因此我们将雷公藤内酯醇(一种具有抗炎特性的化合物)修饰到icLNPs中。雷公藤内酯醇修饰、抗Flt1肽偶联且负载Itgb1-siRNA的icLNPs(Itgb1-siRNA@TPL)在滴眼给药后可有效抑制体外血管内皮细胞的增殖和迁移以及小鼠的CoNV形成。这些作用是通过下调PI3K/AKT和NF-κB信号通路实现的。最后,对Itgb1-siRNA@TPL的生物安全性进行了测试,结果表明它对角膜或主要器官无毒,且对角膜上皮愈合无影响。总之Itgb1-siRNA@TPL代表了一种治疗CoNV的新型、非侵入性且有效的方法。