Yan Huimin, Hu Ying, Akk Antonina, Rai Muhammad Farooq, Pan Hua, Wickline Samuel A, Pham Christine T N
Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
John Cochran Veterans Affairs Medical Center, St. Louis, MO 63106, USA.
Pharmaceutics. 2020 Jan 17;12(1):73. doi: 10.3390/pharmaceutics12010073.
Osteoarthritis (OA) is a progressive joint disease that causes significant disability and pain and for which there are limited treatment options. We posit that delivery of anabolic factors that protect and maintain cartilage homeostasis will halt or retard OA progression. We employ a peptide-based nanoplatform to deliver Wingless and the name Int-1 (WNT) 16 messenger RNA (mRNA) to human cartilage explants. The peptide forms a self-assembled nanocomplex of approximately 65 nm in size when incubated with WNT16 mRNA. The complex is further stabilized with hyaluronic acid (HA) for enhanced cellular uptake. Delivery of peptide-WNT16 mRNA nanocomplex to human cartilage explants antagonizes canonical β-catenin/WNT3a signaling, leading to increased lubricin production and decreased chondrocyte apoptosis. This is a proof-of-concept study showing that mRNA can be efficiently delivered to articular cartilage, an avascular tissue that is poorly accessible even when drugs are intra-articularly (IA) administered. The ability to accommodate a wide range of oligonucleotides suggests that this platform may find use in a broad range of clinical applications.
骨关节炎(OA)是一种渐进性关节疾病,会导致严重的残疾和疼痛,且治疗选择有限。我们认为,递送保护和维持软骨稳态的合成代谢因子将阻止或延缓OA的进展。我们采用基于肽的纳米平台将无翅型和Int-1(WNT)16信使核糖核酸(mRNA)递送至人软骨外植体。该肽与WNT16 mRNA孵育时会形成大小约为65纳米的自组装纳米复合物。该复合物用透明质酸(HA)进一步稳定以增强细胞摄取。将肽-WNT16 mRNA纳米复合物递送至人软骨外植体可拮抗经典的β-连环蛋白/WNT3a信号传导,导致润滑素产生增加和软骨细胞凋亡减少。这是一项概念验证研究,表明mRNA可有效递送至关节软骨,即使在关节内(IA)给药时,关节软骨这种无血管组织也很难到达。容纳多种寡核苷酸的能力表明该平台可能会在广泛的临床应用中得到应用。