Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Sci Rep. 2022 Mar 7;12(1):4015. doi: 10.1038/s41598-022-07969-9.
Mesenchymal stem cells (MSCs) are at the forefront of research for a wide range of diseases, including osteoarthritis (OA). Despite having attracted the attention of orthopedists, current MSC therapy techniques are limited by poor MSC implantation in tissue defects and lack of lateral tissue integration, which has restricted the efficacy of cell therapy to alleviate OA symptoms only. Here, we developed targeted MSC therapy for OA cartilage using a cell-tissue matchmaking nanoconstruct (C-TMN). C-TMN, as an MSC vehicle, consists of a central iron oxide nanoparticle armed with two types of antibodies, one directed at the MSC surface and the other against articular cartilage. We treated rat OA articular cartilage with intra-articular injections of C-TMN with and without exogenous MSCs. We observed substantial improvements in both symptomatic and radiographic OA caused by C-TMN, which was independent of exogenous MSCs. This new approach could predict a promising future for OA management.
间充质干细胞(MSCs)是广泛疾病治疗研究的前沿领域,包括骨关节炎(OA)。尽管已经引起了骨科医生的关注,但目前的 MSC 治疗技术受到 MSC 在组织缺陷中的植入不良和缺乏侧向组织整合的限制,这限制了细胞治疗缓解 OA 症状的效果。在这里,我们使用细胞组织匹配纳米结构(C-TMN)开发了针对 OA 软骨的靶向 MSC 治疗。C-TMN 作为 MSC 载体,由一个中央氧化铁纳米颗粒组成,配备了两种类型的抗体,一种针对 MSC 表面,另一种针对关节软骨。我们通过关节内注射 C-TMN 并用和不用外源性 MSC 治疗大鼠 OA 关节软骨。我们观察到 C-TMN 引起的症状性和放射性 OA 都有显著改善,而这与外源性 MSC 无关。这种新方法可能为 OA 管理带来广阔的前景。