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Expression of osteoprotegerin RNAK and RANKL genes in femoral head avascular necrosis and related signaling pathway

机译:骨保护素RANK和RANKL基因在股骨头缺血性坏死中的表达及相关信号通路

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摘要

Femoral head avascular necrosis (AVN) causes the damage of hip joint and related dysfunctions, thus consisting of a clinical challenge. Osteoprotegerin (OPG), receptor activator of nuclear factor κB (RANK) and its ligand (RANKL) all regulate the formation of bones via gene transcriptional regulation for the balance between osteoblasts and osteoclasts. This study thus investigated the expressional profiles of OPG, RANK and RANKL genes in AVN patients, and explored related molecular mediating pathways. Real-time qPCR was used to measure the gene expression of OPG, RANK and RANKL genes in AVN femoral head tissue samples from 42 patients, along with normal tissues. Western blotting analysis was performed to quantify protein levels of OPG and RANKL. There was a trend but not statistically significant elevation of mRNA levels of OPG in femoral head AVN tissues compared to normal tissues (P>0.05). The expression of RNAK and RNAKL, however, was significantly elevated in necrotic tissues (P<0.05). No significant difference in protein levels of OPG or RANKL between groups. The expression of OPG, RANK and RANKL genes exert a crucial role in the progression of AVN, suggesting their roles in mediating bone homeostasis and potential effects on bone destruction.
机译:股骨头缺血性坏死(AVN)会导致髋关节损伤和相关功能障碍,从而构成临床挑战。骨保护素(OPG),核因子κB受体激活剂(RANK)及其配体(RANKL)都通过基因转录调节骨细胞和破骨细胞之间的平衡,从而调节骨骼的形成。因此,本研究调查了AVN患者中OPG,RANK和RANKL基因的表达情况,并探讨了相关的分子介导途径。实时定量PCR用于测量42例患者的AVN股骨头组织样本以及正常组织中OPG,RANK和RANKL基因的基因表达。进行蛋白质印迹分析以定量OPG和RANKL的蛋白质水平。与正常组织相比,股骨头AVN组织中OPG的mRNA水平有上升趋势,但无统计学意义(P> 0.05)。然而,坏死组织中RNAK和RNAKL的表达显着升高(P <0.05)。两组之间OPG或RANKL的蛋白质水平无显着差异。 OPG,RANK和RANKL基因的表达在AVN的进程中起着至关重要的作用,表明它们在介导骨稳态和对骨破坏的潜在影响中起着重要的作用。

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