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肿瘤坏死因子-α对小鼠骨髓基质细胞护骨素表达的影响 被引量:4

Effects of tumor necrosis factor-alpha on expressions of osteoprotegerin mRNA and OPG protein in mouse marrow stromal MBA-1 cell lines
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摘要 目的 探讨肿瘤坏死因子 -α(TNF- α)对骨髓基质细胞护骨素 (OPG)mRNA和蛋白质表达的影响以及TNF- α在骨代谢中的作用。方法 用TNF- α干预培养的小鼠骨髓基质MBA 1细胞 ,用RT PCR和Westernblot检测TNF- α不同剂量和不同作用时间时OPG表达变化。结果 ①MBA- 1细胞表达OPG ;②TNF -α对MBA- 1细胞OPGmRNA和OPG蛋白质表达有下调作用 ,但无剂量和时间依赖性 ;③ 17- β雌二醇 (17- βE2 )能阻断TNF α对MBA 1细胞OPG表达的下调作用 ;而吡咯二硫氨基甲酸酯 (PDTC ,一种核因子 κB抑制剂 )不能拮抗此作用。结论 TNF -α下调OPG表达。雌激素拮抗TNF- α,使MBA 1细胞OPG表达上调。TNF -α对OPG表达的影响与转录因子 - κB信息通路无关。 Objective To observe the effects of tumor necrosis factor-alpha (TNF-α) on the expressions of osteoprotegerin (OPG) in mouse bone marrow stromal MBA-1 cells, and investigate the potential roles of TNF-α in the pathogenesis of osteoporosis. Methods The expressions of OPG mRNA and OPG protein was assayed by RT-PCR and Western blot in BMA-1 cells treated with TNF-α in different concentrations and at different time-periods of cultures. Results (1) OPG was expressed in BMA-1 cell lines. (2) TNF-α downregulated the expression of OPG in BMA-1 cells in a dose-and time-independent manner. (3) 17β-estradiol suppressed the downregulation of TNF-α on the expression of OPG, whereas pyrrodine dithiocarbamete (PDTC) (inhibitor of nuclear factor-κB) had no effects on its downregulation. Conclusions TNF-α enhances osteoclastic bone resorption and bone loss by decreasing the expression of OPG in bone marrow stromal MBA-1 cells. The mechanism involved in the therapeutic effect of estrogen may associate with the suppression of OPG expression, but the signaling pathway that regulates OPG expression by TNF-α is not involved in the activation of nuclear fcator-κB.
出处 《中国骨质疏松杂志》 CAS CSCD 2005年第1期1-4,16,共5页 Chinese Journal of Osteoporosis
基金 国家自然科学基金资助项目 (3 9970 3 47)
关键词 OPG TNF-α 蛋白质表达 护骨素 骨髓基质细胞 小鼠 肿瘤坏死因子-Α 影响 拮抗 RNA Bone marrow stromal cells Osteoprotegerin Tumor necrosis factor-α Osteoprotegerin 17β-estradiol
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  • 1Pfeilschifter J, Koditz R, Pfohl M, et al. Changes in proinflammatory cytokine activity after menopause. Endocri Rev, 2002; 23: 90-119.
  • 2Yasuda H, Shima N, Nakagawa N, et al. Identity of osteoclastogenesis inhibitory factor (OCIF) and osteoprotegerin (OPG) :a mechanism by which OPG/OCIF inhibits osteoclastogenesis in vitro. Endocrinology,1998, 139: 1329-1337.
  • 3Saika M, Inoue D, Kido S, et al. 17 β-estradiol stimulates expression of osteoprotegerin by a mouse stromal cell line, ST-2, via estrogen receptor-a. Endocrinology, 2001, 142:2205-2212.
  • 4Hsu H, Lacey DL, Dunstan CR, et al. Tumor necrosis factor receptor family member RNA mediates osteoclast differentiation and activation induced by osteoprotegerin ligand. Proc Natl Acad Sci USA, 1999,96: 3540-3545.
  • 5O'Brien CA, Gubrij I, LinSC, etal. STAT activation in stromal/osteoblast cells is required for induction of the receptor activator of NF-kappa B ligand and stimulation of osteoclastogenesis by gp 130-utilizing cytokines or interleukin-1 but not 1, 25-dihydroxyvitamin D3 or parathyroid hormone. J Biol Chem, 1999,274: 19301-19308.
  • 6Bucay N, Sarosi I, Dunstan CR, et al. Osteoprotegerin- deficiefit mice develop early onset osteoporosis and arterial calcification. Genes Dev,1998,12:1260-1268.
  • 7Kimble RB, Srivastava S, Ross FP, et al. Estrogen deficiency inceases the ability of stromal cells to support murine osteoclastogenesis via an interleukin-1 and tumor necrosis factor-mediated stimulation of macrophage colony-stimulating factor production. J Biol Chem, 1996,271: 28890-28897.
  • 8陶惠人,王全平,李寰.甲状旁腺素相关肽对骨髓基质细胞中RANKL及OPG基因的表达影响[J].中华风湿病学杂志,2004,8(2):77-79. 被引量:4
  • 9Hofbauer LC, Khosla S, Dunstan CR, et al. Estrogen stimulates gene expression and protein production of osteoprotegerin in human osteoblastic cells. Endocrinology, 1999, 140:4367-4370.
  • 10Baldwin AJ. The NF-kappa B and I kappa B proteins: New discoveries and insights. Annu Rev Immunol, 1996, 14: 649-683.

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