State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, Hefei, Anhui, China.
Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100021, China.
Cell Death Dis. 2018 Feb 12;9(2):214. doi: 10.1038/s41419-017-0254-6.
This study aimed to investigate the role of protein phosphatase 5 (PP5) on bone and cartilage development using both in vivo and in vitro approaches. Six- to 8-week- old male PP5 knockout mice (KO) and their wild-type (WT) littermate controls were randomly selected for this study, and their body weights and bone (femur) lengths were measured. Micro-computed tomography scanning (Micro-CT) was performed to determine femoral bone density and micro-architecture. Mesenchymal stem cells (MSCs) isolated from bone marrow were used to examine the effects of PP5 on osteogenesis in vitro. Whole-mount Alcian blue and Alizarin red staining were used to detect cartilage formation in newborn vertebrae, limbs, and feet. Hematoxylin and eosin (H&E) staining was performed to determine growth plate thickness. Real-time PCR analysis, western blotting, and immunohistochemistry were used to detect the expression of genes and proteins in bone marrow-derived MSCs as well as in bone and cartilage tissues. The results showed PP5 KO mice exhibited significantly reduced body weight and shorter femur length compared to WT controls. The KO mice also had significantly higher volumetric bone mineral density (BMD), trabecular bone volume, and cortical thickness in the femur. The deficiency of PP5 significantly enhanced the formation of cartilage in vertebrae, limbs, and feet. In addition, KO mice possessed a wider distal femur growth plates containing significantly more chondrocytes than WT mice. Furthermore, higher expressions of several cartilage-specific genes were observed in the articular cartilage of PP5 KO mice. Immunohistochemical labeling of growth plates demonstrated that phospho-PPARγ, Runx1, and Runx2 levels were considerably higher in the KO mice. In conclusion, PP5 is a significant negative regulator on the regulation of bone and cartilage development.
本研究旨在通过体内和体外方法研究蛋白磷酸酶 5(PP5)在骨骼和软骨发育中的作用。选择 6-8 周龄雄性 PP5 敲除(KO)小鼠及其野生型(WT)同窝对照小鼠进行本研究,并测量其体重和骨骼(股骨)长度。进行微计算机断层扫描(Micro-CT)以确定股骨骨密度和微观结构。分离自骨髓的间充质干细胞(MSCs)用于体外研究 PP5 对成骨的影响。使用全骨骼茜素红和阿尔新蓝染色来检测新生椎骨、四肢和足部的软骨形成。进行苏木精和伊红(H&E)染色以确定生长板的厚度。实时 PCR 分析、Western blot 和免疫组织化学用于检测骨髓源性 MSC 以及骨和软骨组织中基因和蛋白的表达。结果表明,与 WT 对照组相比,PP5 KO 小鼠的体重明显减轻,股骨长度明显缩短。KO 小鼠的股骨体积骨矿物质密度(BMD)、小梁骨体积和皮质厚度也显著增加。PP5 的缺乏显著增强了椎骨、四肢和足部的软骨形成。此外,KO 小鼠的远端股骨生长板更宽,含有比 WT 小鼠更多的软骨细胞。此外,在 PP5 KO 小鼠的关节软骨中观察到几个软骨特异性基因的表达水平更高。生长板的免疫组织化学标记表明,KO 小鼠中的磷酸化-PPARγ、Runx1 和 Runx2 水平明显更高。总之,PP5 是骨骼和软骨发育调节的重要负调控因子。