Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan, ROC.
Biomaterials. 2011 Oct;32(28):6773-80. doi: 10.1016/j.biomaterials.2011.05.080. Epub 2011 Jun 23.
The aim of this study was to develop a new diagnostic and therapeutic approach for the treatment of osteoporosis. Previously, we demonstrated that intraosseous transplantation of platelet-rich plasma (PRP) treated-osteoblast-like cells into ovariectomized senescence-accelerated mice (OVX-SAMP8) prevented the development of osteoporosis. In continuation, we aimed to explore the complex etiology of osteoporosis using this platform. An inverse relationship between bone marrow adipogenesis and osteogenesis has been suggested in the development of osteoporosis but the underlying mechanisms remain poorly described. To address these issues, we used PRP to inhibit adipocyte differentiation by promoting osteoblastic differentiation in adipocytes. In addition, a positive correlation between an increase in bone marrow adipocytes and bone loss was established. We assessed this relationship using an osteoporotic animal disease model which consisted of young (for prevention) and old (for treatment) OVX-SAMP8 mice. This animal model demonstrated that PRP treatment mainly exerted its action via promoting bone regeneration but also appeared to suppress adipogenesis within the marrow. The findings and methodology of this study could potentially be applied in the prevention and treatment of osteoporosis.
本研究旨在为骨质疏松症的治疗开发一种新的诊断和治疗方法。此前,我们证明了将富含血小板的血浆(PRP)处理的成骨样细胞经骨内移植到去卵巢加速衰老小鼠(OVX-SAMP8)中可预防骨质疏松症的发生。在此基础上,我们旨在利用该平台探索骨质疏松症的复杂病因。有人提出,在骨质疏松症的发生过程中,骨髓脂肪生成与成骨之间呈负相关,但潜在机制仍描述不清。为了解决这些问题,我们使用 PRP 通过促进脂肪细胞中的成骨细胞分化来抑制脂肪细胞分化。此外,还建立了骨髓脂肪细胞增加与骨丢失之间的正相关关系。我们使用包括年轻(用于预防)和年老(用于治疗)OVX-SAMP8 小鼠在内的骨质疏松动物疾病模型来评估这种关系。该动物模型表明,PRP 治疗主要通过促进骨再生来发挥作用,但似乎也抑制了骨髓中的脂肪生成。本研究的发现和方法有可能应用于骨质疏松症的预防和治疗。