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作 者:刘欣[1] 林良妍[1] 赵霞[1] 乔珍[1] 綦才辉[1] 金勇君[1]
机构地区:[1]山东省滨州医学院烟台附属医院内分泌科,,264100
出 处:《中华内分泌代谢杂志》2013年第1期83-85,共3页Chinese Journal of Endocrinology and Metabolism
基 金:国家自然科学基金资助项目(30660070);山东省中青年科学家科研奖励基金资助项目(BS2010YY002)
摘 要:以核因子κB受体活化因子配体(RANKL)和促黑素(α-MSH)孵育Raw264.7细胞6d,经抗酒石酸酸性磷酸酶染色观察破骨细胞形成的数目.并检测酸性磷酸酶活性。RT-PCR检测Raw264.7细胞5种黑皮质素受体(MCR)的表达。结果显示,与RANKL组相比较,RANKL+α—MSH组显著增加了破骨细胞的形成数量(P〈0.05),呈剂量依赖性,单独应用α—MSH组未见破骨细胞形成。RANKL组和RANKL+α-MSH组的酸性磷酸酶活性显著高于对照组和α-MSH组(P〈0.05),但前2组之间差异无统计学意义(P〉0.05);RT—PCR结果显示Raw264.7细胞5种MCR均表达。结果提示,α-MSH可能通过RANK信号通路促进破骨细胞形成。Raw264.7 cells were incubated with receptor activator of NV-kappa B ligand (RANKL) and α- melanocyte stimulating hormone(α-MSH) for6 d. The amount of osteoclast cells were counted by tartrate resistant acid phosphatase staining and the acid phosphatase activity was assayed. The expressions of 5 melanocortin receptors (MCR) in Raw264.7 cells were determined by RT-PCR. The results showed that the number of osteoclasts in RANKL +α-MSH group was significantly increased compared with RANKL group (P 〈 0.05 ), but there was no osteoclast formation in α-MSH group. Compared with control group and α-MSH group, the acid phosphatase activities were significantly increased in RANKL group and α-MSH+RANKL group ( P〈0.05 ). All five MCRs were expressed in the Raw264.7 cells shown by RT-PCR. These results suggest that α-MSH may promote osteoclasts formation through RANK signaling pathway.
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