骨关节炎
信使核糖核酸
软骨
细胞外基质
细胞生物学
下调和上调
转染
翻译(生物学)
医学
癌症研究
化学
生物
病理
生物化学
基因
解剖
替代医学
作者
M J Sun,Bin Ma,Zihang Pan,Yun Zhao,Liangliang Tian,Yifei Fan,Weijing Kong,Junyan Wang,Boyang Xu,Yingfang Ao,Quanyi Guo,Xi Wang,Xiaohong Peng,Xiaoxia Li,Cheng Jin,Lei Miao,Kai Wang,Xiaoqing Hu
标识
DOI:10.1002/adhm.202400804
摘要
Abstract Fibroblast growth factor 18 (FGF18) emerges as a promising therapeutic target for osteoarthritis (OA). In this study, a novel articular cavity‐localized lipid nanoparticle (LNP) named WG‐PL14 is developed. This optimized formulation has a nearly 30‐fold increase in mRNA expression as well as better articular cavity enrichment compared to commercial lipids MC3 when performing intra‐articular injection. Then, a mRNA sequence encoding recombinant human FGF18 (rhFGF18) for potential mRNA therapy in OA is optimized. In vitro assays confirm the translation of rhFGF18 mRNA into functional proteins within rat and human chondrocytes, promoting cell proliferation and extracellular matrix (ECM) synthesis. Subsequently, the therapeutic efficacy of the LNP‐rhFGF18 mRNA complex is systematically assessed in a mouse OA model. The administration exhibits several positive outcomes, including an improved pain response, upregulation of ECM‐related genes (e.g., AGRN and HAS2), and remodeling of subchondral bone homeostasis compared to a control group. Taken together, these findings underscore the potential of localized LNP‐rhFGF18 mRNA therapy in promoting the regeneration of cartilage tissue and mitigating the progression of OA.
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