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基质金属蛋白酶在ARDS发病机制中的作用 被引量:3

Effect of matrix metalloproteinases in the pathogenesis of acute respiratory distress syndrome
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摘要 基质金属蛋白酶是一组结构和功能相似、锌依赖性内肽酶的总称,主要功能是降解细胞外基质。ARDS是以顽固性低氧血症、非心源性肺水肿及炎症反应的过度与失控为特点的急性呼吸衰竭综合征。基质金属蛋白酶可通过蛋白水解作用激活并释放细胞因子及化学因子、破坏肺泡一上皮细胞屏障完整性、激活蛋白酪氨酸激酶(protein tyrosine kinases,PTKs)信号通路等作用促进ARDS的发生、发展。 Matrix metalloproteinases,a large family of zinc-dependent endopeptidases,are the main function to degrade the extracellular matrix. Acute respiratory distress syndrome(ARDS), a syndrome of acute respiratory failure, is characterized by refractory hypoxemia, noncardiogenic pulmonary edema and dysregulated and excessive inflammation. Matrix metalloproteinases can promote the occurrence and development of ARDS by proteolytic processing,including cytokines and chemical factors activation and release,destruction of the integrity of alveolar-epithelial barrier and activation of the protein tyrosine kinase signaling pathway.
出处 《国际呼吸杂志》 2015年第24期1906-1909,共4页 International Journal of Respiration
关键词 基质金属蛋白酶 急性呼吸窘迫综合征 细胞外基质 细胞因子 信号通路 Matrix Metalloproteinases Acute Respiratory Distress Syndrome Extracellular Matrix Cytokine Signaling Pathway
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  • 1Matthay MA, Zemans RL. The acute respiratory distresssyndrome:pathogenesis and treatment[J]. Annu Rev Pathol,2011,6:147-163.
  • 2Matthay MA,Ware LB,Zimmerman GA. The acuterespiratory distress syndrome [J ]. J Clin Invest,2012,122(8):2731-2740.
  • 3Burnham EL, Janssen WJ,Riches DW, et al. Thefibroproliferative response in acute respiratory distresssyndrome: mechanisms and clinical significance [J]. EurRespir J,2014,43 (1):276-285.
  • 4Ranieri VM, Rubenfeld GD, Thompson BT, et al. ARDSDefinition Task Force. Acute respiratory distress syndrome:the Berlin Definition[J]. JAMA,2012 ,307 .23) : 2526-2533.
  • 5Herridge MS,Tansey CM, Matte A,et al. Functionaldisability 5 years after acute respiratory distress syndrome[J]. N Engl J Med,201 1 ,364 C14) : 1293-1304.
  • 6Ware LB* Koyama T, Zhao Z,et al. Biomarkers of lungepithelial injury and inflammation distinguish severe sepsispatients with acute respiratory distress syndrome [J]. CritCare,2013,17 C5):R253.
  • 7Huang W, McCaig LA, Veldhuizen RA,et al. Mechanismsresponsible for surfactant changes in sepsis-induced lunginjury[J]. Eur Respir J,2005,26 (6) : 1074-1079.
  • 8Schmidt EP, Lee WL, Zemans RL, et al. On,around, andthrough : neutrophil-endothelial interactions in innateimmunity[J]. Physiology (Bethesda) ,2011,26 .5) :334-347.
  • 9Zemans RL, Colgan SP,Downey GP. Transepithelialmigration of neutrophils : mechanisms and implications foracute lung injury [J]. Am J Respir Cell Mol Biol, 2009 , 40.5):519-535.
  • 10Davey A, McAuley DF, O, Kane CM. Matrixmetalloproteinases in acute lung injury: mediators of injuryand drivers of repair[J]. Eur Respir J,2011,38(4):959-970.

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