线粒体应激信号的神经内分泌协调和蛋白质稳定
Kristen M Berendzen1, Jenni Durieux1, Li-Wa Shao2
1The Glenn Center for Aging Research, Howard Hughes Medical Institute, Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Cell
|September 10, 2016
概括
神经退行性疾病导致广泛的代谢变化. 这项研究揭示了由血清素传播的神经元应激信号,
科学领域:
- 神经生物学
- 细胞生物学
- 代谢调节
背景情况:
- 神经退行性疾病涉及有毒的蛋白质聚合物和全身代谢改变.
- 关联中枢神经系统应激与周围代谢变化的机制尚不清楚.
- 神经元中的蛋白质毒性压力可能会通过内分泌信号触发全身反应.
研究的目的:
- 研究神经元应激在蛋白质毒性疾病期间调节线粒体平衡中的作用.
- 阐明参与神经元蛋白质毒性的系统反应的信号通路.
主要方法:
- 使用C. elegans作为研究蛋白质聚合和神经元应激的模型生物.
- 研究聚合性蛋白与线粒体的相互作用.
- 评估了线粒体未折叠蛋白反应 (UPR) 的诱导.
- 检查了密集核心囊泡释放和血清素分泌在信号传播中的作用.
主要成果:
- 神经元中的聚合性蛋白与线粒体结合,诱导全球UPR.
- 这种线粒体反应会影响整个动物的生理.
- 血清激素的分泌对于压力信号的传播至关重要.
- 这些发现表明营养感应网络被选中用于器官间通信.
结论:
- 神经蛋白质毒性压力可以通过UPR诱导全身代谢变化.
- 在神经元中传递线粒体压力的过程中, serotonin 的作用至关重要.
- 这种机制突出了细胞间交流的新途径,
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