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PPARγ及其配体与类风湿关节炎的研究进展 被引量:1

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摘要 过氧化物酶体增殖物激活受体(Peroxisome proliferater-activated receptor,PPAR)是一类由配体活化的核转录因子,属于细胞核受体超家族。PPAR被配体激活后参与体内多种生理及病理生理过程,对调节体内的多种代谢过程有重要作用。本文综述了PPARγ的结构及其组织分布、配体、相关信号转导途径以及类风湿关节炎的近年概况,并在此基础上,提出了PPARγ信号通路对类风湿关节炎发病机制的作用,为疾病治疗寻找靶点。
作者 郑可 崔向军
出处 《海南医学》 CAS 2011年第16期110-112,共3页 Hainan Medical Journal
基金 湖北省自然科学基金(编号:2009CDB113)
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参考文献21

  • 1Issemann I, Green S. Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferator [J]. Nature, 1990. 347(6294): 645-650.
  • 2Knapp P, Jarzabek KB, Achnio A, et al. The role of per-oxisome pro- liferator-activated receptors (PPAR) in carcinogenesis [J]. Ginekol Pol, 2006, 77(8): 643-651.
  • 3Greene ME, Blumberg B, Mc Bride OW, et al. Isolation of the hu- man peroxisome proliferator activated receptor gamma cDNA: ex- pression in hematopoietic cells and chromosomal mapping [J]. Gene Expr, 1995, 4: 281-299.
  • 4Vamecq J, Latruff N. Medical significance of peroxisome prolifera- tor-activated receptors [J]. Lancet, 1999, 354: 141-8.
  • 5Shao D, Rangwala SM, Bailey ST, et al. Interdomain communica- tion regulating ligand binding by PPAR-gamma [J]. Nature, 1998, 396: 377-380.
  • 6Elbrecht A, Chen Y, CuUinan CA, et al. Molecular cloning expres- sion and characterization of human peroxisome proliferators activat- ed receptors gamma 1 and gamma 2 [J]. Biochem Biophys Res Commun, 1996, 224(2): 431-437.
  • 7Willson TM, Brown PJ, Sternbach DD, et al. The PPARs from or- phan receptors to drug discovery [J]. J Med Chem, 2000, 43(4): 527-550.
  • 8Forman BM, Tontonoz P, Chen J, et al. 15-Deoxy-delta 12,14-pros- taglandin J2 is a ligand for the adipocyte determination factor PPAR gamma [J]. Cell, 1995, 83(5): 803-812.
  • 9葛恒,王长谦.PPAR配体作用机制及新配体筛选研究进展[J].中国药学杂志,2004,39(3):170-172. 被引量:7
  • 10Fajas L, Auboeuf D, Raspe E, et al. The organization promoter anal- ysis and expression of the human PPAR-gamma gene [J]. J Biol Chem, 1997, 272(30): 18779-18789.

二级参考文献26

  • 1[1]Berger J, Moller DE. The mechanisms of action of PPARs [J]. Annu Rev Med, 2002,53:409.
  • 2[2]Wurtz JM, Bourguet W, Renaud JP, et al. A canonical structure for the ligand-binding domain of nuclear receptors [J]. Nature Structural Biology, 1996,3(1):87.
  • 3[3]Xu HE, Lambert MH, Montana VG, et al. Structural determinants of ligand binding selectivity between the peroxisome proliferator-activated receptors [J]. Proc Nati Acad Sci USA, 2001,98(24): 13919.
  • 4[4]Kliewer SA, Sundseth SS, Jones SA, et al. Fatty acids and eicosanoids regulate gene expression through direct interactions with peroxisome proliferator-activated receptors alpha and gamma [J]. Proc Nati Acad Sci USA, 1997,2994(9) :4318.
  • 5[5]Zhu Y, Qi C, Calandra C, et al. Cloning and identification of mouse steroid receptor coactivator-1 ( mSRC-1 ), as a coactivator of peroxisome proliferator-activated receptor gamma [ J ]. Gene Expression,1996,6(3): 185.
  • 6[6]Zhu Y, Qi C, Jain S, et al. Isolation and characterization of PBP, a protein that interacts with peroxisome proliferator-activated receptor[J]. J Biol Chem, 1997,272(41):25500.
  • 7[7]Heery DM, Kalkhoven E, Hoare S, et al. A signature motif in transcriptional co-activators mediates binding to nuclear receptors [ J ].Nature, 1997,387(6634) :733.
  • 8[8]Oberkofier H, Esterbaner H, Linnemayr V, et al. Peroxisome proliferators-activated receptor gamma coactivator-1 recruitment regulated PPAR subtype specificity [J]. J Biol Chem, 2002,277(19): 17650.
  • 9[9]Oberfield JL, Collins JL, Holmes CP, etal. A peroxiseme prolfferator-activated receptor gamma ligand inhibits adipocyte differentiation[J]. Proc Nati Acad Sci USA, 1999,96(11) :6102.
  • 10[10]Wurch T, Junquero D, Delhon A, et al. Pharmcological analysis of wild-type alpha, gamma and delta subtypes of the human peroxisome proliferator-activated receptor [ J ]. Naunyn Schmiedebergs Arch Pharmacol, 2002,365(2): 133.

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