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10.3892/mmr.2017.6564

http://scihub22266oqcxt.onion/10.3892/mmr.2017.6564
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C5482130!5482130!28498469
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suck abstract from ncbi


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pmid28498469      Mol+Med+Rep 2017 ; 16 (1): 231-7
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  • Expression of c-FLIP in a rat model of sepsis and its effects on endothelial apoptosis #MMPMID28498469
  • Shen L; Sun Z; Zhao F; Wang W; Zhang W; Zhu H
  • Mol Med Rep 2017[Jul]; 16 (1): 231-7 PMID28498469show ga
  • Sepsis is characterized by the impaired regulation of inflammatory responses. Apoptosis is important in the pathogenesis of sepsis. Cellular FLICE-inhibitory protein (c-FLIP) is a catalytically inactive caspase-8 homologue, which negatively interferes with apoptotic signaling. The role of c-FLIP in sepsis and in endothelial cell apoptosis, a critical step in the pathogenesis of sepsis, remains controversial. In the present study, to investigate the relationship between c-FLIP and sepsis, a rat model of sepsis was induced by cecal ligation and puncture, and western blot analysis was used to detect the expression of c-FLIPL, the long isoform of c-FLIP. Lower protein expression levels of c-FLIPL were found in the brain, intestine and lung of the rat sepsis model, compared with the rats in the sham surgery group. The association between the expression of c-FLIPL and endothelial cell apoptosis was further examined in vitro by c-FLIPL overexpression and flow cytometry, which demonstrated that the expression of c-FLIPL was inversely correlated with endothelial cell apoptosis. These data suggested that c-FLIP may be important in sepsis and shed light on therapeutic strategies.
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