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内皮细胞蛋白C受体与脓毒症关系的研究进展 被引量:2

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摘要 脓毒症是临床常见、由感染引起的全身性炎症反应综合征(SIRS),易发展成为严重脓毒症和脓毒症休克,甚至多器官功能障碍(M ODS )。其病情发展迅速、治疗费用高,医疗资源消耗大,病死率高[1‐2]。在脓毒症病情发展过程中,凝血系统的紊乱、尤其蛋白C系统功能的异常尤为突出。蛋白C系统主要包括蛋白C(PC)、内皮细胞蛋白C受体(EPCR)、蛋白S(PS)血栓调节蛋白(T M )及凝血酶,其终产物均为活化蛋白 C (APC)。EPCR参与了PC的活化和脓毒症的发生发展过程,下文简述EPCR的一般性质及其在脓毒症中的作用。
出处 《重庆医学》 CAS 北大核心 2016年第27期3867-3870,共4页 Chongqing medicine
基金 国家自然科学基金资助项目(81560321) 2014年广西医学高层次骨干人才培养"139"计划培养人选项目 广西高校急重症分子免疫研究重点实验室项目(yy2015ky002) 广西研究生教育创新计划项目(YCSZ2015222)
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参考文献42

  • 1付圆.脓毒症发病机制的研究进展[J].中国现代医生,2014,52(11):155-157. 被引量:29
  • 2Mayr FB,Yende S,Angus DC. Epidemiology of severesepsis[J]. Virulence,2014,5(l) :4-11.
  • 3Laszik Z^Mitro A,Taylor FB,et al. Human protein C re-ceptor is present primarily on endothelium of large bloodvessels : implications for the control of the protein C path-way[J], Circulation, 1997 ,96( 10) : 3633-3640.
  • 4Gleeson EM, 0/ donnell JS,Preston RJ. The endothelialcell protein C receptor:cell surface conductor of cytopro-tective coagulation factor signaling[J].Cell Mol Life Sci,2012,69(5) :717-726.
  • 5Simmonds RE,Lane DA. Structural and functional impli-cations of the intron/exon organization of the human en-dothelial cell protein C/activated protein C receptor(EPCR) gene : comparison with the structure of CD1/ma-jor histocompatibility complex alphal and alpha2 domains[J]. Blood,1999,94(2):632-641.
  • 6Hayashi T, Nakamura H,Okada A, et al. Organizationand chromosomal localization of the human endothelialprotein C receptor gene[J]. Gene, 1999,238(2) *367-373.
  • 7Ranee JB, Follows GA,Cockerill PN, et al. Regulation ofthe human endothelial cell protein C receptor gene pro-moter by multiple Spl binding sites [J]. Blood,2003,101(11):4393-4401.
  • 8Yin G,Jin X,Ming H,et al. Endothelial cell protein C re-ceptor gene 6936A/G polymorphism is associated withvenous thromboembolism[J]. Exp Ther Med,2012,3(6):989-992.
  • 9Vassiliou AG?Maniatis NA,Kotanidou A,et al. Endothe-lial protein C receptor polymorphisms and risk of severesepsis in critically ill patients [J]. Intensive Care Med,2013,39(10):1752-1759.
  • 10Medina P,Navarro S, Estelles A, et al. Polymorphisms intheendothelial proteinC receptor gene and thrombophilia[J]. Thromb Haemost,2007,98(3) *564-569.

二级参考文献71

  • 1衡伟,王兆钺.内皮蛋白C受体及其病理与临床意义[J].国际输血及血液学杂志,2006,29(1):9-12. 被引量:3
  • 2衡伟,王兆钺,白霞,戴兰,沈文红,董宁征.肺癌细胞系内皮蛋白C受体的表达及其意义[J].苏州大学学报(医学版),2006,26(5):788-792. 被引量:3
  • 3FUKUDOME K, ESMON C T, Identification, cloning, and regulation of a novel endothelial cell protein C/activated protein C receptor[J]. J Biol Chem, 1994, 269: 26486-26491.
  • 4O'BRIEN L A, RICHARDSON M A, MEHRBOD S F, et al. Activated protein C decreases tumor necrosis factor related apoptosis-indueing ligand by an EPCR- independent mechanism involving Egr-1/Erk-1/2 activation [ J]. Arterioscier Thromb Vasc Biol, 2007, 27: 2634-2641.
  • 5TAYLOR F, PEER G T, LOCKHAR M S, et al. Endothelial cell protein C receptor plays an important role in protein C activation in vivo. Blood, 2001, 97: 1685-1688.
  • 6IAKHIAEV A V, REZAIE A R, Idell S. Thrombomodulinmediated catabolism of protein C by pleural mesothelial and vascular endothelial cells[J]. Thromb Haemost, 2007, 98: 627-634.
  • 7Medina P, Navarro S, Estelles A, et al. Polymorphisms in the endothelial protein C receptor gene and thrombophilia[J]. Thromb Haemost, 2007, 98: 564-569.
  • 8GUPTA A, RHODES GJ, BERG D T, et al. Activated protein C ameliorates LPS-induced acute kidney injury and downregulates renal INOS and angiotensin 2[J]. Am J Physiol Renal Physiol, 2007, 293: F245.
  • 9OKAJIMA K. Prevention of endothelial cell injury by activated protein C: the molecular mechanism(s) and therapeutic implications[J]. Curr Vase Pharmacol, 2004,2 : 125-133.
  • 10XUE M, MARCH L, SAMBROOK P N, et al, Differential regulation of matrix metalloproteinase 2 and matrix metalloproteinase 9 by activated protein C: relevance to inflammation in rheumatoid arthritis[J]. Arthritis Rheum, 2007, 56: 2864- 2874.

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