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山东大学学报(医学版) ›› 2014, Vol. 52 ›› Issue (3): 56-58.doi: 10.6040/j.issn.1671-7554.0.2013.344

• 基础医学 • 上一篇    下一篇

促黑素对小鼠成骨细胞OPG/RANKLmRNA表达的影响

乔珍1,綦才辉1,杨美子2,金勇君1   

  1. 1. 滨州医学院烟台附属医院内分泌科,山东 烟台 264100; 2. 滨州医学院药理学教研室,山东 烟台 264003
  • 收稿日期:2013-05-26 出版日期:2014-03-10 发布日期:2014-03-10
  • 通讯作者: 金勇君。E-mail:endojin@126.com
  • 基金资助:

    国家自然科学基金(30660070);山东省中青年科学家科研奖励基金(BS2010YY002)

Effect of α-melanocyte stimulating hormone on the expressions of OPG and  RANKL mRNA in mouse osteoblasts

QIAO Zhen1, QI Caihui1, YANG Meizi2, JIN Yongjun1   

  1. 1.Department of Endocrinology, Yantai Affilicated Hospital of Binzhou Medical University, Yantai 264100, Shandong, China;
    2. Department of Pharmacology, Binzhou Medical University, Yantai 264003, Shandong, China
  • Received:2013-05-26 Online:2014-03-10 Published:2014-03-10

摘要:

目的  探讨原代培养的小鼠成骨细胞黑皮质素受体(MCR)表达的种类及促黑素(α-MSH)对其骨保护素(OPG)和核因子-κB受体活化因子配体(RANKL)mRNA表达的影响。方法  酶消化法分离3d内新生C57BL/6小鼠原代成骨细胞,培养液中分别加入10-7、10-8和10-9mol/L的α-MSH培养12h,作为A、B、C组;培养液中加入10-7mol/L α-MSH,分别培养6、12、24h,作为D、E、F组。对照组正常培养。采用实时定量PCR方法  分析α-MSH对成骨细胞OPG/RANKL mRNA表达的影响。利用RT-PCR法测定原代成骨细胞MCR的表达。结果  小鼠原代成骨细胞表达MC1R、MC2R、MC4R和MC5R;与对照组相比,α-MSH促进OPG/RANKL mRNA的表达(P<0.05)。结论  α-MSH可能通过MCR系统促进小鼠原代成骨细胞OPG/RANKL mRNA的表达。

关键词: 促黑素;骨保护素;核因子-&kappa, B受体活化因子配体;黑皮质素受体

Abstract:

Objective  To investigate the types of melanocortin receptor (MCR) of the primary osteoblasts, and the effect of α-melanocyte stimulating hormone (α-MSH) on the expressions of osteoprotegerin (OPG) and receptor activator of nuclear factor-kappa B ligand (RANKL) mRNA in  mouse osteoblasts. Methods  Calvarial osteoblasts were separated and cultured in vitro by the mechanical separation and enzyme digestion method. The primary osteoblasts were divided into groups A, B and C, which were treated with 10-7, 10-8 and 10-9 mol/L α-MSH respectively for 12 h; the primary osteoblasts were divided into groups D, E and F, which were treated with 10-7 mol/L α-MSH for 6, 12 and 24h respectively. Control group was set up at the same time. The expressions of OPG and RANKL mRNA were detected by Real-Time PCR. MCR subtypes in the primary osteoblasts were measured by RT-PCR. Results  MC1R, MC2R, MC4R and MC5R were expressed in primary cultured osteoblasts.The expressions of OPG and RANKL mRNA significantly increased after incubation with α-MSH (P<0.05). Conclusion  α-MSH might promote the expressions of OPG and RANKL mRNA in the primary osteoblasts through MCR system.

Key words: Osteoprotegerin, Recetor activator nuclear factor-kappa B ligand, Melanocortin receptor, α-melanocyte stimulating hormone

中图分类号: 

  • R581.9
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