Wu Yun, Ma Junyu, Woods Parker S, Chesarino Nicholas M, Liu Chang, Lee L James, Nana-Sinkam Serge P, Davis Ian C
Dept. of Biomedical Engineering, State University of New York at Buffalo, Bonner Hall, Buffalo, NY 14260, USA; Nanoscale Science and Engineering Center for Affordable Nanoengineering of Polymeric Biomedical Devices, The Ohio State University, Smith Laboratory, 174W. 18th Ave., Columbus, OH 43210, USA.
Nanoscale Science and Engineering Center for Affordable Nanoengineering of Polymeric Biomedical Devices, The Ohio State University, Smith Laboratory, 174W. 18th Ave., Columbus, OH 43210, USA.
J Control Release. 2015 Apr 10;203:140-9. doi: 10.1016/j.jconrel.2015.02.016. Epub 2015 Feb 14.
Alveolar type II (ATII) respiratory epithelial cells are essential to normal lung function. They may be also central to the pathogenesis of diseases such as acute lung injury, pulmonary fibrosis, and pulmonary adenocarcinoma. Hence, ATII cells are important therapeutic targets. However, effective ATII cell-specific drug delivery in vivo requires carriers of an appropriate size, which can cross the hydrophobic alveolar surfactant film and polar aqueous layer overlying ATII cells, and be taken up without inducing ATII cell dysfunction, pulmonary inflammation, lung damage, or excessive systemic spread and side-effects. We have developed lipoplexes as a versatile nanoparticle carrier system for drug/RNA delivery. To optimize their pulmonary localization and ATII cell specificity, lipoplexes were conjugated to an antibody directed against the ATII cell-specific antigen surfactant protein-C (SP-C) then administered to C57BL/6 mice via the nares. Intranasally-administered, anti-SP-C-conjugated lipoplexes targeted mouse ATII cells with >70% specificity in vivo, were retained within ATII cells for at least 48h, and did not accumulate at significant levels in other lung cell types or viscera. 48h after treatment with anti-SP-C-conjugated lipoplexes containing the test microRNA miR-486, expression of mature miR-486 was approximately 4-fold higher in ATII cells than whole lung by qRT-PCR, and was undetectable in other viscera. Lipoplexes induced no weight loss, hypoxemia, lung dysfunction, pulmonary edema, or pulmonary inflammation over a 6-day period. These findings indicate that ATII cell-targeted lipoplexes exhibit all the desired characteristics of an effective drug delivery system for the treatment of pulmonary diseases that result primarily from ATII cell dysfunction.
肺泡II型(ATII)呼吸上皮细胞对正常肺功能至关重要。它们可能也是急性肺损伤、肺纤维化和肺腺癌等疾病发病机制的核心。因此,ATII细胞是重要的治疗靶点。然而,在体内实现有效的ATII细胞特异性药物递送需要合适大小的载体,该载体能够穿过疏水的肺泡表面活性物质膜和覆盖在ATII细胞上的极性水层,并被摄取而不引起ATII细胞功能障碍、肺部炎症、肺损伤或过度的全身扩散及副作用。我们已开发出脂质体作为一种用于药物/RNA递送的通用纳米颗粒载体系统。为了优化其肺部定位和ATII细胞特异性,将脂质体与针对ATII细胞特异性抗原表面活性蛋白C(SP-C)的抗体偶联,然后通过鼻孔给予C57BL/6小鼠。经鼻给药后,抗SP-C偶联脂质体在体内对小鼠ATII细胞的靶向特异性>70%,在ATII细胞内保留至少48小时,且在其他肺细胞类型或内脏中无明显积聚。在用含有测试微小RNA miR-486的抗SP-C偶联脂质体处理48小时后,通过qRT-PCR检测,ATII细胞中成熟miR-486的表达比全肺高约4倍,在其他内脏中未检测到。脂质体在6天内未引起体重减轻、低氧血症、肺功能障碍、肺水肿或肺部炎症。这些发现表明,靶向ATII细胞的脂质体展现出了一种有效药物递送系统的所有理想特性,可用于治疗主要由ATII细胞功能障碍导致的肺部疾病。