Department of Orthopaedics, Wuhan Third Hospital-Tongren Hospital of Wuhan University, Wuhan, China.
Wuhan Sports University, Wuhan, China.
FASEB J. 2019 Jul;33(7):8055-8068. doi: 10.1096/fj.201801618RRR. Epub 2019 Apr 9.
Traumatic osteonecrosis of the femoral head (ONFH) is a condition leading to the collapse of the femoral head, and the primary treatment is a total hip replacement, which has a poor prognosis. The current study was conducted with the aim of investigating the role of exosomes from bone marrow-derived mesenchymal stem cells (BM-MSCs) carrying microRNA-224-3p (miR-224-3p) in traumatic ONFH. Initially, a microarray analysis was performed to screen the differentially expressed genes and miRs associated with traumatic ONFH. Patients with traumatic and nontraumatic ONFH were enrolled, and HUVECs were obtained. The BM-MSCs-derived exosomes were purified and characterized, after which HUVECs were cocultured with exosomes. The functional role of miR-224-3p in traumatic ONFH was determined using ectopic expression, depletion, and reporter assay experiments. Endothelial cell proliferation, migration, invasion abilities, and angiogenesis were evaluated. Based on microarray analysis, miR-224-3p was found to be down-regulated, whereas focal adhesion kinase family interacting protein of 200 kDa (FIP200) was up-regulated in ONFH. Traumatic ONFH exosomes resulted in the up-regulation of FIP200 and down-regulation of miR-224-3p. FIP200 was confirmed to be a target gene of miR-224-3p. Exosomes were internalized by vascular endothelial cells. The down-regulation of exosomal miR-224-3p was observed to promote endothelial cell proliferation, migration, invasion abilities, angiogenesis, and FIP200 expression. In addition, FIP200 overexpression promoted angiogenesis. In summary, the results highly indicated that lower miR-224-3p levels in exosomes derived from BM-MSCs promote angiogenesis of traumatic ONFH by up-regulating FIP200. The present study provides a potential strategy for the treatment of traumatic ONFH.-Xu, H.-J., Liao, W., Liu, X.-Z., Hu, J., Zou, W.-Z., Ning, Y., Yang, Y., Li, Z.-H. Down-regulation of exosomal microRNA-224-3p derived from bone marrow-derived mesenchymal stem cells potentiates angiogenesis in traumatic osteonecrosis of the femoral head.
创伤性股骨头坏死(ONFH)是导致股骨头塌陷的一种病症,其主要治疗方法是全髋关节置换,但预后较差。本研究旨在探讨携带 microRNA-224-3p(miR-224-3p)的骨髓间充质干细胞(BM-MSCs)来源的外泌体在创伤性 ONFH 中的作用。首先,进行了微阵列分析,以筛选与创伤性 ONFH 相关的差异表达基因和 miRs。招募创伤性和非创伤性 ONFH 患者,并获得 HUVECs。纯化和表征 BM-MSCs 来源的外泌体,然后将 HUVECs 与外泌体共培养。通过异位表达、耗尽和报告基因检测实验确定 miR-224-3p 在创伤性 ONFH 中的功能作用。评估内皮细胞增殖、迁移和侵袭能力以及血管生成。基于微阵列分析,发现 miR-224-3p 下调,而粘着斑激酶家族相互作用蛋白 200kDa(FIP200)上调在 ONFH 中。创伤性 ONFH 外泌体导致 FIP200 上调和 miR-224-3p 下调。FIP200 被确认为 miR-224-3p 的靶基因。外泌体被血管内皮细胞内化。观察到外泌体 miR-224-3p 的下调促进内皮细胞增殖、迁移、侵袭能力、血管生成和 FIP200 表达。此外,FIP200 过表达促进血管生成。总之,结果高度表明,BM-MSCs 来源的外泌体中 miR-224-3p 水平降低通过上调 FIP200 促进创伤性 ONFH 的血管生成。本研究为创伤性 ONFH 的治疗提供了一种潜在策略。