Department of Orthopaedics, Shanghai Key Laboratory of Orthopaedic Implant, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200011, China; Department of Orthopaedics, Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan 410012, China.
Department of Orthopaedics, Shanghai Key Laboratory of Orthopaedic Implant, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200011, China.
Biochem Pharmacol. 2014 Aug 1;90(3):276-87. doi: 10.1016/j.bcp.2014.06.009. Epub 2014 Jun 17.
Osteoclast-induced bone resorption and wear-particle-induced osteolysis leads to prosthetic loosening, one of the most common causes of joint implant failure, resulting in revision surgery. Thus, inhibition of osteoclastic bone resorption, which further prevents wear particle-induced osteolysis, is a potential treatment strategy for prosthetic loosening. Here, we examined the therapeutic effect of hypericin (HP), which was photosensitive, on osteoclastogenesis and wear particle-induced osteolysis in the absence of visible light. HP inhibited RANKL-induced osteoclast differentiation in bone marrow macrophages (BMMs) and RAW264.7 cell line without any evidence of cytotoxicity. The bone-resorbing activity of mature osteoclasts was significantly inhibited by HP. As HP has been previously reported to inhibit signalling pathway such as ERK and NF-κB in other cells, which is also important in osteoclast differentiation. We thus examined the molecular mechanism and showed that HP significantly inhibited the ERK/mitogen-activated protein kinase (MAPK) signalling pathway without affecting nuclear factor kappaB (NF-κB), c-Jun N-terminal kinase (JNK) and p38 signalling in RANKL-stimulated BMMs. Further in vivo studies revealed HP attenuated osteoclast formation and subsequently prevented wear particle-induced bone erosion. Taken together, the results suggest that HP inhibits RANKL-mediated osteoclastogenesis via affecting ERK signalling in vitro and suppresses wear particle-induced osteolysis in vivo. We therefore conclude that HP may be an innovative and safe alternative treatment for osteoclast-related prosthetic loosening.
破骨细胞诱导的骨吸收和磨损颗粒诱导的骨溶解导致假体松动,这是关节植入物失效的最常见原因之一,导致翻修手术。因此,抑制破骨细胞的骨吸收,从而进一步防止磨损颗粒诱导的骨溶解,是治疗假体松动的一种潜在策略。在这里,我们研究了血卟啉(HP)的治疗效果,HP 是一种光敏剂,可在没有可见光的情况下抑制破骨细胞的形成和磨损颗粒诱导的骨溶解。HP 抑制 RANKL 诱导的骨髓巨噬细胞(BMM)和 RAW264.7 细胞系中的破骨细胞分化,没有任何细胞毒性的证据。成熟破骨细胞的骨吸收活性被 HP 显著抑制。由于 HP 以前曾被报道在其他细胞中抑制 ERK 和 NF-κB 等信号通路,这些信号通路在破骨细胞分化中也很重要。因此,我们检查了分子机制,并表明 HP 显著抑制了 ERK/丝裂原活化蛋白激酶(MAPK)信号通路,而不影响核因子 kappaB(NF-κB)、c-Jun N-末端激酶(JNK)和 RANKL 刺激的 BMM 中的 p38 信号通路。进一步的体内研究表明,HP 减弱了破骨细胞的形成,随后防止了磨损颗粒诱导的骨侵蚀。总之,这些结果表明,HP 通过影响体外 RANKL 介导的破骨细胞分化中的 ERK 信号通路来抑制破骨细胞的形成,并在体内抑制磨损颗粒诱导的骨溶解。因此,我们得出结论,HP 可能是一种创新的、安全的治疗与破骨细胞相关的假体松动的替代方法。