Article Summary
崔敏萱,王文文,向 安,杨 媛,卢兹凡,汪 莉.线粒体来源肽MOTS-c通过抑制促炎性因子分泌改善脓毒症小鼠生存率[J].现代生物医学进展英文版,2019,19(15):2839-2844.
线粒体来源肽MOTS-c通过抑制促炎性因子分泌改善脓毒症小鼠生存率
Mitochondrial-derived Peptide MOTS-c Improves Survival in Septic Mice Via Reducing Pro-inflammatory Cytokine Production
Received:January 26, 2019  Revised:February 22, 2019
DOI:10.13241/j.cnki.pmb.2019.15.008
中文关键词: 线粒体来源肽  MOTS-c  脓毒症
英文关键词: Mitochondrial-derived peptide  MOTS-c  Sepsis
基金项目:国家肿瘤重点实验室自主课题(CBSKL2017Z18)
Author NameAffiliationE-mail
CUI Min-xuan Company 16, battalion 4, Student Brigade, School of Basic Medicine, Air Force Military Medical University, Xi'an, Shaanxi, 710032, China cuiminxuan0430@163.com 
WANG Wen-wen State Key Laboratory of Cancer Biology, Department of Biopharmaceutics, School of Pharmacy, Air Force Military Medical University, Xi'an, Shaanxi, 710032, China  
XIANG An State Key Laboratory of Cancer Biology, Department of Biopharmaceutics, School of Pharmacy, Air Force Military Medical University, Xi'an, Shaanxi, 710032, China  
YANG Yuan State Key Laboratory of Cancer Biology, Department of Biopharmaceutics, School of Pharmacy, Air Force Military Medical University, Xi'an, Shaanxi, 710032, China  
LU Zi-fan State Key Laboratory of Cancer Biology, Department of Biopharmaceutics, School of Pharmacy, Air Force Military Medical University, Xi'an, Shaanxi, 710032, China  
WANG Li State Key Laboratory of Cancer Biology, Department of Biopharmaceutics, School of Pharmacy, Air Force Military Medical University, Xi'an, Shaanxi, 710032, China  
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中文摘要:
      摘要 目的:研究一种新的线粒体来源肽MOTS-c对脓毒症小鼠生存率的影响。方法:构建了LPS和CLP诱导的两种脓毒症小鼠模型,观察MOTS-c治疗对小鼠生存率及促炎性因子TNF-α和IL-6水平的影响。Western-blot方法检测MOTS-c对巨噬细胞NF-κB活化的影响。结果:与对照组相比,MOTS-c治疗使LPS诱导的脓毒症小鼠生存率从10%提高至60% (P<0.05),而CLP诱导的脓毒症小鼠生存率则从10%提高至50% (P<0.05)。ELISA结果显示,在LPS诱导的脓毒症模型中,MOTS-c治疗使小鼠血浆中的TNF-α和IL-6的水平显著降低(P<0.05);与之类似,在CLP诱导的脓毒症模型中,小鼠血浆和腹腔灌洗液中的TNF-α和IL-6的水平也显著下降(P<0.05)。机制研究结果表明,MOTS-c能够显著抑制巨噬细胞中LPS诱导的转录因子NF-κB的活化。结论:MOTS-c能够提高脓毒症小鼠的生存率,其机制可能与抑制NF-κB的转录激活、降低体内促炎性细胞因子的水平相关。
英文摘要:
      ABSTRACT Objective: This study aimsto explore the effects of a mitochondrial-derived peptide MOTS-c treatmenton survival in septic mice. Methods: Two models of sepsis were constructed, one due to lipopolysaccharide (LPS) and the other to cecal ligation and puncture (CLP). The survival rate and pro-inflammatory cytokine levels were detected and compared in septic mice. The influence of MOTS-c on LPS-induced NF-κB activation in macrophages was also analyzed by western-blot. Results: Compared to control group, MOTS-c treatment increased the mice survival rate from 10% to 60% in LPS-induced model(P<0.05), and from 10% to 50% in CLP-induced sepsis (P<0.05)separately. The levels of TNF-α and IL-6 in mice blood plasm were decreased in both two septic models by ELISA analysis. Moreover, MOTS-c treatment reduced the TNF-α and IL-6 concentration in peritoneal fluid of CLP-induced septic mice(P<0.05). Mechanically, the NF-αB activation was suppressed by MOTS-c in LPS challenged macrophages. Conclusion: Our data indicated that MOTS-c could inhibit the activation of NF-κB and suppress the expression of pro-inflammatory cytokines, thus leading to increased survival in septic mice.
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