期刊文献+

泛素-蛋白酶体抑制剂对动脉粥样硬化的影响 被引量:1

下载PDF
导出
摘要 目前很多研究证实,动脉粥样硬化是血管壁对各类损伤刺激的异常反应,是动脉壁的慢性炎症性疾病。炎性反应贯穿动脉粥样硬化形成和发展的每个阶段,且炎症机制还与动脉粥样硬化的多种并发症的产生存在密切关系。血管平滑肌细胞为血管壁的重要组成部分,在血管收缩及舒张方面起着重要的调节作用,它同时也分泌多种细胞因子和炎性介质。血管平滑肌细胞的炎症可诱导平滑肌细胞的增殖与迁移,最终导致血管动脉粥样硬化病变和血管外科手术后再狭窄等问题。泛素-蛋白酶体系统参与机体内炎性反应过程,且泛素-蛋白酶体抑制剂可通过抑制血管平滑肌的炎性反应,从而抑制动脉粥样硬化的发生。目前已证实,多种抗动脉粥样硬化药物具有抗炎功能,抗炎治疗已成为防治动脉粥样硬化的一种新策略。本文对泛素-蛋白酶体抑制剂对动脉粥样硬化的影响机制做一综述。
出处 《医学研究杂志》 2016年第7期21-24,共4页 Journal of Medical Research
基金 黑龙江省自然科学基金资助项目(H201306)
  • 相关文献

参考文献2

二级参考文献41

  • 1Raasi S, Wolf D H. Ubiquitin receptors and ERAD: A network of pathways to the proteasome [ J ]. Semin Cell Dev Biol, 2007,18 (6) :78 -91.
  • 2Fricke B, Heink S, Steffen J, et al. The proteasome maturation protein POMP facilitates major steps of 20S proteasome formation at the endoplasmic reticulum[ J]. EMBO Rep, 2007,8(12) :1170 - 5.
  • 3Meiners S, Ludwig A, Stangl V, et al. Proteasome inhibitors: Poisons and remedies [ J ]. Med Res Rev, 2008,28 (2) :309 - 27.
  • 4Marques A J, Glanemann C, Ramos P C, et al. The C-terminal extension of the beta 7 subunit and activator complexes stabilize nascent 20s proteasomes and promote their maturation [ J ]. J Biol Chem, 2007,282 (48) :34869 - 76.
  • 5Kim H T, Kim K P, Lledias F, et al. Certain pairs of ubiquitinconjugating enzymes (E2s) and ubiquitin-protein ligases (E3s) synthesize nondegradable forked ubiquitin chains containing all possible isopeptide linkages [ J ]. J Biol Chem, 2007. 282 ( 24 ) : 17375 - 86.
  • 6Kwon Y T, Kashina A S, Varshavsky A. Alternative splicing resuits in differential expression, activity, and localization of the two forms of arginyl-tRNA-protein transferase, a component of the Nend rule pathway [ J ]. Mol Cell Biol, 1999.19 (1) : 182 -93.
  • 7Ludwig H, Khayat D, Giaccone G, et al. Proteasome inhibition and its clinical prospects in the treatment of hematologic and solid malignancies[ J]. Cancer, 2005. 104(9) : 1794 - 807.
  • 8lnoue J, Gohda J, Akiyama T, et al. NF-kappaB activation in development and progression of cancer [ J ]. Cancer Sci, 2007.98 (3) : 268 - 2674.
  • 9Adams J. The development of proteasome inhibitors as antieaneer drugs[J]. Cancer Cell, 2004.5(5) : 417 -21.
  • 10Sasaki M, Nie L, Maki C G. MDM2 binding induces a conformational change in p53 that is opposed by heat-shock protein 90 and precedes p53 proteasomal degradation[ J]. J Biol Chem, 2007. 282 (19) : 14626-34.

共引文献44

同被引文献9

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部