[1]刘丹,尹东,汤蕾,等.LPS预处理对心肌细胞缺氧/复氧损伤的保护作用[J].第三军医大学学报,2012,34(17):1707-1710.
 Liu Dan,Yin Dong,Tang Lei,et al.Protective effect of lipopolysaccharide pretreatment on cardiomyocytes anoxia/reoxygenation injury[J].J Third Mil Med Univ,2012,34(17):1707-1710.
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LPS预处理对心肌细胞缺氧/复氧损伤的保护作用(/HTML )
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《第三军医大学学报》[ISSN:1000-5404/CN:51-1095/R]

卷:
34卷
期数:
2012年第17期
页码:
1707-1710
栏目:
论著
出版日期:
2012-09-15

文章信息/Info

Title:
Protective effect of lipopolysaccharide pretreatment on cardiomyocytes anoxia/reoxygenation injury
作者:
刘丹尹东汤蕾孙惦许旻何明
南昌大学医学院:药理教研室,第二附属医院江西省分子医学重点实验室
Author(s):
Liu Dan Yin Dong Tang Lei Sun Dian Xu Ming He Ming
Department of Pharmacology, School of Medical College, Jiangxi Provincial Key Laboratory of Molecular Medicine,  Second Affiliated Hospital, Nanchang University, Nanchang, Jiangxi Province, 330006, China
关键词:
14-3-3γ内毒素耐受缺氧/复氧损伤RNA干扰
Keywords:
14-3-3γ endotoxin tolerance anoxia/reoxygenation injury RNAi
分类号:
R394-33; R394.2; R542.2
文献标志码:
A
摘要:
目的       探讨14-3-3γ基因在LPS预处理对抗心肌细胞缺氧/复氧(A/R)损伤中的作用。      方法       构建pSUPER/14-3-3γ RNA干扰重组质粒,转染入心肌细胞,分为5组:对照组、A/R组、LPS+A/R组、pSUPER+LPS+A/R组、pSUPER/14-3-3γ+LPS+A/R组。Western blot检测14-3-3γ蛋白表达,生化自动分析仪测定乳酸脱氢酶(LDH)活性,MTT法测定细胞存活率,流式细胞仪检测细胞凋亡,线粒体肿胀实验检测线粒体通透性转换孔(mPTP)开放。      结果       A/R损伤使细胞存活率下降,LDH升高,细胞凋亡增加,mPTP开放;LPS预处理可使14-3-3γ表达明显增加,通过抑制mPTP开放,对A/R损伤的细胞有保护作用;pSUPER/14-3-3γ RNA干扰重组质粒通过抑制14-3-3γ蛋白表达,取消LPS预处理的保护作用。      结论       LPS预处理可对抗心肌细胞缺氧/复氧损伤,其机制与上调14-3-3γ,从而抑制mPTP开放有关。
Abstract:
Objective       To explore the role of 14-3-3γ gene in the protection of cardiomyocytes with lipopolysaccharide (LPS) pretreatment against anoxia/reoxygenation (A/R) injury.       Methods       A RNA interference (RNAi) recombinant plasmid of pSUPER/14-3-3γ was constructed and transferred into cardiomyocytes. The cardiomyocytes were divided into five groups including a control group, an A/R group, a LPS+A/R group, a pSUPER+LPS+A/R group and a pSUPER/14-3-3γ+LPS+A/R group. The protein level of 14-3-3γ was detected by Western blotting. The activity of lactate dehydrogenase (LDH) was determined by an automated biochemical analyzer. Cell viability was analyzed by MTT assay. Cell apoptosis was measured by flow cytometry. The opening of mitochondrial permeability transition pore (mPTP) was determined by swelling of isolated cardiac mitochondria.       Results       The A/R damage resulted in cell viability decrease, LDH and cell apoptosis increase, and mPTP opening. The LPS pretreatment up-regulated 14-3-3γ protein expression and protected cardiomyocytes against A/R injury through inhibiting the mPTP opening. The pSUPER/14-3-3γ RNAi recombinant plasmid could reduce 14-3-3γ protein expression and then reverse the protective effect of LPS pretreatment.       Conclusion       LPS pretreatment may have a protective effect on cardiomyocytes subjected to A/R injury, and its mechanism may be related to 14-3-3γ upregulation and subsequent mPTP opening inhibition.

参考文献/References:

刘丹, 尹东, 汤蕾, 等. LPS预处理对心肌细胞缺氧/复氧损伤的保护作用[J].第三军医大学学报,2012,34(17):1707-1710.

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[1]陈太忠,张艳,熊弢,等.脂多糖预处理对GSK-3功能活性的影响[J].第三军医大学学报,2012,34(13):1304.
 Chen Taizhong,Zhang Yan,Xiong Tao,et al.Effect of LPS pretreatment on GSK-3 functional activity in rats[J].J Third Mil Med Univ,2012,34(17):1304.

更新日期/Last Update: 2012-08-31