贝克林-1-依赖性自保护心脏在败血症期间
Yuxiao Sun1, Xiao Yao1, Qing-Jun Zhang2
1Departments of Surgery (Y.S., X.Y., D.C., S.E.W., J.P.M., Q.S.Z.), University of Texas Southwestern Medical Center, Dallas.
Circulation
|June 2, 2018
概括
在败血症期间,贝克林-1-依赖性自会保护心脏. 激活Beclin-1信号改善了心脏功能和减少了炎症,这表明了毒引起的心脏功能障碍的潜在治疗策略.
科学领域:
- 心血管生物学
- 细胞生物学
- 分子医学
背景情况:
- 败血症引起的心脏功能障碍是多器官衰竭的关键组成部分.
- 心脏自在败血症发病过程中的确切作用尚不清楚.
- 目前尚未开发出针对自的治疗方法.
研究的目的:
- 在败血症期间调查Beclin-1依赖心脏自.
- 探索针对败血症自途径的治疗潜力.
主要方法:
- 使用了一种由脂聚糖 (LPS) 诱导的败血症小鼠模型.
- 使用心脏特异性的Beclin-1过度表达和Beclin-1随机充足.
- 使用细胞透性Tat-Beclin-1来激活自.
主要成果:
- 通过高剂量激活哺乳动物的拉巴胺素 (mTOR),以剂量依赖的方式调节自.
- 贝克林- 1过度表达改善了心脏功能,抑制了mTOR,并减少了炎症和纤维化.
- Beclin-1 保护了线粒体,减少了与危险相关的分子模式,并促进了线粒体消化.
- 在患有LPS的小鼠中,使用Tat- Beclin-1改善了心脏功能并减轻了炎症.
结论:
- 在败血症期间,Beclin-1 在心脏中起着保护作用.
- 针对Beclin-1信号的诱导代表了与败血症相关的心脏功能障碍的有希望的治疗途径.
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