基础医学与临床
基礎醫學與臨床
기출의학여림상
Basic & Clinical Medicine
2015年
2期
178-182
,共5页
刘威%段林%许光明%于峰%张晓静%宋宁
劉威%段林%許光明%于峰%張曉靜%宋寧
류위%단림%허광명%우봉%장효정%송저
胆囊收缩素%脂多糖%C/EBP同源蛋白%caspase-11%caspase-1
膽囊收縮素%脂多糖%C/EBP同源蛋白%caspase-11%caspase-1
담낭수축소%지다당%C/EBP동원단백%caspase-11%caspase-1
cholecystokinin%lipopolysaccharides%C/EBP homologous protein%caspase-11%caspase-1
目的:探讨CCK-8对LPS激活RAW264.7细胞CHOP/caspase-11/caspase-1信号通路的影响。方法用LPS和(或) CCK-8和(或) CCK-8的1受体阻滞剂孵育RAW 264.7细胞,用Western blot法检测CHOP、caspase-11蛋白表达,用试剂盒检测caspase-1活性,用ELISA技术检测细胞培养上清中IL-1β水平。结果与对照组相比,LPS组CHOP、caspase-11表达水平均显著升高( P<0.05),给予CCK-8可有效抑制LPS诱导的CHOP、caspase-11表达升高( P<0.05),而预先给予CCK-8的1受体阻滞剂可明显抑制CCK-8的作用。 caspase-1活性变化、IL-1β含量变化趋势均与CHOP、caspase-11表达水平变化趋势一致( P<0.05)。结论 CCK-8通过受体1抑制CHOP/caspase-11/caspase-1表达,减少LPS诱导IL-1β的生成,发挥抗炎作用。
目的:探討CCK-8對LPS激活RAW264.7細胞CHOP/caspase-11/caspase-1信號通路的影響。方法用LPS和(或) CCK-8和(或) CCK-8的1受體阻滯劑孵育RAW 264.7細胞,用Western blot法檢測CHOP、caspase-11蛋白錶達,用試劑盒檢測caspase-1活性,用ELISA技術檢測細胞培養上清中IL-1β水平。結果與對照組相比,LPS組CHOP、caspase-11錶達水平均顯著升高( P<0.05),給予CCK-8可有效抑製LPS誘導的CHOP、caspase-11錶達升高( P<0.05),而預先給予CCK-8的1受體阻滯劑可明顯抑製CCK-8的作用。 caspase-1活性變化、IL-1β含量變化趨勢均與CHOP、caspase-11錶達水平變化趨勢一緻( P<0.05)。結論 CCK-8通過受體1抑製CHOP/caspase-11/caspase-1錶達,減少LPS誘導IL-1β的生成,髮揮抗炎作用。
목적:탐토CCK-8대LPS격활RAW264.7세포CHOP/caspase-11/caspase-1신호통로적영향。방법용LPS화(혹) CCK-8화(혹) CCK-8적1수체조체제부육RAW 264.7세포,용Western blot법검측CHOP、caspase-11단백표체,용시제합검측caspase-1활성,용ELISA기술검측세포배양상청중IL-1β수평。결과여대조조상비,LPS조CHOP、caspase-11표체수평균현저승고( P<0.05),급여CCK-8가유효억제LPS유도적CHOP、caspase-11표체승고( P<0.05),이예선급여CCK-8적1수체조체제가명현억제CCK-8적작용。 caspase-1활성변화、IL-1β함량변화추세균여CHOP、caspase-11표체수평변화추세일치( P<0.05)。결론 CCK-8통과수체1억제CHOP/caspase-11/caspase-1표체,감소LPS유도IL-1β적생성,발휘항염작용。
Objective To investigate the effect of CCK-8 on CHOP/caspase-11/caspase-1 expressions induced by LPS in RAW264.7 cells.Methods RAW264.7 cells were incubated with LPS and/or CCK-8 and/or CCK-8 1R blocking agent devazepide for indicated times .CHOP and caspase-11 protein expressions were determined by West-ern blot , caspase-1 activity was analyzed by kit , IL-1βexpression level was analyzed by ELISA .Results Both CHOP and caspase-11 expression were upregulated in LPS-activated RAW264.7 cell, which were inhibited by pre-treatment of CCK-8 .Pre-treatment of devazepide inhibited the effects of CCK-8 significantly .The same effects were found in caspase-1 activity and IL-1βexpression .Conclusions CCK-8 exerts an anti-inflammatory effect by inhib-iting CHOP/caspase-11/caspase-1 expressions induced by LPS in RAW264.7 cell.CCK 1R may contribute to the anti-inflammatory effect of CCK-8.