Moriya Shuichi, Izu Yayoi, Arayal Smriti, Kawasaki Makiri, Hata Koki, Pawaputanon Na Mahasarakhahm Chantida, Izumi Yuichi, Saftig Paul, Kaneko Kazuo, Noda Masaki, Ezura Yoichi
Department of Molecular Pharmacology, Tokyo Medical and Dental University, Tokyo, Japan.
Department of Orthopaedic Surgery, Juntendo University School of Medicine, Japan.
J Cell Physiol. 2016 May;231(5):1163-70. doi: 10.1002/jcp.25214. Epub 2015 Nov 10.
Unloading induces bone loss and causes disuse osteoporosis. However, the mechanism underlying disuse osteoporosis is still incompletely understood. Here, we examined the effects of cathepsin K (CatK) deficiency on disuse osteoporosis induced by using sciatic neurectomy (Nx) model. After 4 weeks of surgery, CatK KO and WT mice were sacrificed and subjected to analyses. For cancellous bone rich region, Nx reduced the bone mineral density (BMD) compared to the BMD in the sham operated side in wild type mice. In contrast, CatK deficiency suppressed such Nx-induced reduction of BMD in cancellous bone. Nx also reduced BMD in the mid shaft cortical bone compared to the BMD in the corresponding region on the sham operated side in wild type mice. In contrast, CatK deficiency suppressed such Nx-induced reduction of BMD in the mid shaft cortical bone. Bone volume (BV/TV) was reduced by Nx in WT mice. In contrast, Cat-K deficiency suppressed such reduction in bone volume. Interestingly, CatK deficiency suppressed osteoclast number and osteoclast surface in the Nx side compared to sham side. When bone marrow cells obtained from Nx side femur of CatK-KO mice were cultured, the levels of the calcified area in culture were increased. Further examination of gene expression indicated that Nx suppressed the expression of genes encoding osteoblast-phenotype-related molecules such as Runx2 and alkaline phosphatase in WT mice. In contrast, CatK deficiency suppressed such reduction. These data indicate that CatK is involved in the disuse-induced bone mass reduction.
去负荷会导致骨质流失并引发废用性骨质疏松。然而,废用性骨质疏松的潜在机制仍未完全明确。在此,我们利用坐骨神经切除术(Nx)模型,研究了组织蛋白酶K(CatK)缺乏对废用性骨质疏松的影响。手术4周后,处死CatK基因敲除(KO)小鼠和野生型(WT)小鼠并进行分析。对于富含松质骨的区域,与野生型小鼠假手术侧的骨矿物质密度(BMD)相比,Nx降低了BMD。相比之下,CatK缺乏抑制了Nx诱导的松质骨BMD降低。与野生型小鼠假手术侧相应区域的BMD相比,Nx也降低了骨干皮质骨的BMD。相比之下,CatK缺乏抑制了Nx诱导的骨干皮质骨BMD降低。WT小鼠中,Nx降低了骨体积(BV/TV)。相比之下,Cat-K缺乏抑制了骨体积的这种降低。有趣的是,与假手术侧相比,CatK缺乏抑制了Nx侧破骨细胞数量和破骨细胞表面积。当培养从CatK-KO小鼠Nx侧股骨获得的骨髓细胞时,培养物中钙化面积水平增加。对基因表达的进一步检测表明,Nx抑制了野生型小鼠中编码成骨细胞表型相关分子(如Runx2和碱性磷酸酶)的基因表达。相比之下,CatK缺乏抑制了这种降低。这些数据表明,CatK参与了废用诱导的骨量减少。
J Cell Physiol. 2016-5