期刊文献+

RIP3-依赖性细胞坏死在脓毒症中研究进展 被引量:1

原文传递
导出
摘要 脓毒症(sepsis)是一种严重感染引起的全身炎症反应[1-2],它可以被看作是从感染到多器官功能障碍综合征的持续恶化[3].在美国,脓毒症是重症监护病房中非心脏病死亡的首要原因,每年发病超过80万人,病死率高达30%[4],花费占美国总住院费的39%[5],但仍缺乏有效的治疗手段.脓毒症的致病机制尚不清楚,促炎和抗炎细胞因子失衡在脓毒症的发生和发展中起着重要作用.近年来研究发现,蛋白激酶3 (receptor interaction protein kinase 3,RIP3)-依赖性细胞坏死是这一过程的重要参与者.本文综述了RIP3参与的细胞坏死信号途径以及RIP3-依赖性细胞坏死在脓毒症中作用机制的研究进展.
作者 于璐 徐峰
出处 《中华急诊医学杂志》 CAS CSCD 北大核心 2015年第11期1302-1305,共4页 Chinese Journal of Emergency Medicine
  • 相关文献

参考文献34

  • 1Levy MM, Fink MP, Marshall JC, et al. 2001 sccm/esicm/accp/ ats/sis international sepsis definitions conference [ J ]. Intensive Care Med, 2003, 29 (4) : 530-538.
  • 2Bone RC, Balk RA, Cerra FB, et al. Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. The ACCP/SCCM Consensus Conference Committee. American College of Chest Physicians/Society of Critical Care Medicine [J]. Chest, 1992, 101 (6): 1644-1655.
  • 3Annane D, Bellissant E, Cavaillon JM. Septic shock [ J]. Lancet, 2005, 365 (9453): 63-78.
  • 4Dellinger RP, Levy MM, Cadet JM, et al. Surviving Sepsis Campaign: international guidelines for management of severe sepsis and septic shock: 2008 [J]. Intensive Care Med, 2008, 34 (1): 17-60.
  • 5Gaieski DF, Edwards JM, Kallan M J, et al. Benchmarking the incidence and mortality of severe seps!s in the United States [ J ]. Crit Care Me, 2013, 41 (5) : 1167-1174.
  • 6Galluzzi L, Kroemer G. Necroptosis: a specialized pathway of programmed necrosis [J]. Cell, 2008, 135 (7) : 1161-1163.
  • 7Zhang DW, Shao J, Lin J, et al. RIP3, an energy metabolism regulator that switches TNF-indueed cell death from apoptosis to necrosis [J]. Science, 2009, 325 (5938): 332-336.
  • 8Cho YS, Challa S, Moquin D, et al. Phosphorylation-driven assembly of the RIP1-RIP3 complex regulates programmed necrosis and virus-induced inflammation [ J ]. Cell, 2009, 137 ( 6 ) : 1112-1123.
  • 9He S, Wang L, Miao L, et al. Receptor interacting protein kinase- 3 determines cellular necrotic response to TNF-α [ J]. Cell, 2009, 137 (6) : 1100-1111.
  • 10Stanger BZ, Leder P, Lee TH, et al. RIP: a novel protein containing a death domain that interacts with Fas/APO-1 ( CD95 ) in yeast and causes cell death [J]. Cell, 1995, 81 (4) : 513- 523.

二级参考文献11

  • 1Moss M, Martin GS. A global perspective on the epidemiology of sepsis [J]. Intensive Care Med,2004, 30(4) :527-529.
  • 2Nasraway SA. The problems and challenges of immunotheraphy in sepsis [J]. Chest,2003,123(5 Suppl) :451-459.
  • 3张文彤.多重线性回归模型[M].//张文彤.SPSS统计分析高级教程.北京:高等教育出版社,2004:106-111.
  • 4Napolitano LM. Immune stimulation in sepsis: to be or not to be? [ J ]. Chest,2005,127(6) : 1882-1885.
  • 5Ren Y, Wang JD, Xia J, et al. The alterations of mouse plasma proteins during septic development[J]. J proteome Res,2007,6(7) :2812-2821.
  • 6Carrigan SD, Scott G, Tabrizian M. Toward resolving the challenges of sepsis diagnosis[J]. Clinical Chemistry,2004,50(8) : 1301-1314.
  • 7Calvano SE,Xiao WZ,Richards DR,et al.A network-based analysis of systemic inflammation in humans[ J ]. Nature, 2005,437 ( 7061 ) : 1032-1037.
  • 8Pachot A, Monneret G, Voirin N, et al. Longitudinal study of cytokine and immune transcription factor mRNA expression in septic shock[J]. Clinical Immunology, 2005,114 ( 1 ) : 61-69.
  • 9Payen D, Faivre V, Lukaszewicz AC, et al. Assessment of immtmological status in the critically ill[ J ]. Minerva Anestesiol,2000,66(10) : 757-763.
  • 10Saban MR, Hellmich H, Nguyen N, et al. Time course of LPS-induced gene exprseeion in a mouse model of genitourinary inflammation [ J ]. Physiol Genomics,2001,5(3) : 147-160.

共引文献31

同被引文献3

引证文献1

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