与年龄相关的线粒体翻译障碍通过运动和PGC-1α减轻
Laura M de Smalen1, Anastasiya Börsch1, Aurel B Leuchtmann1
1Biozentrum, University of Basel, Basel CH-4056, Switzerland.
概括
萨科佩尼亚通过破坏线粒体蛋白质稳定性来损害肌肉功能. 运动改善了老化肌肉中的线粒体翻译,突出了它在缓解与年龄相关的肌肉损失方面的作用.
科学领域:
- 肌肉生理学 肌肉生理学
- 线粒体生物学 线粒体生物学
- 衰老的研究研究.
背景情况:
- 标志着与年龄相关的骨肌肉质量和功能下降的萨科佩尼亚与线粒体功能障碍和蛋白质稳定不平衡有关.
- 肌肉衰老中这些线粒体过程之间的精确调节联系尚不清楚.
研究的目的:
- 为了研究衰老对骨肌肉中线粒体蛋白质稳定性的影响.
- 阐明控制肌肉衰老期间线粒体转换的调节机制.
- 为了确定运动对线粒体蛋白质稳定性的影响,在sarcopenia的背景下.
主要方法:
- 在sarcopenic骨肌模型中分析线粒体蛋白质稳定.
- 对过氧酶增殖器激活受体 γ 协活性剂 1 α (PGC-1α) 和雌激素相关受体 α (ERRα) 的调节作用的研究.
- 对线粒体翻译和质量控制途径的运动干预措施的评估.
主要成果:
- 萨科佩尼克肌肉表现出线粒体翻译的显著损害.
- 确定PGC-1α和ERRα是这种线粒体翻译障碍的关键调节者.
- 运动训练逆转了与年龄相关的线粒体翻译缺陷,并增强了质量控制机制.
结论:
- 线粒体蛋白质稳定在骨肌肉衰老和肉症的发展中至关重要.
- PGC-1α和ERRα的失调有助于衰老肌肉中的线粒体功能受损.
- 身体活动有效地恢复了线粒体的翻译和质量控制,强调了它对抗萨尔科佩尼亚的治疗潜力.
更多相关视频
06:53Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase COX/SDH Double-labeling Histochemistry
Published on: November 23, 2011
36.8K
07:18Author Spotlight: New Insights into PBMC Mitochondrial Responses Using Fluorespirometry
Published on: May 24, 2024
1.1K
相关概念视频
Mitochondria
13.8K
Mitochondria are eukaryotic cellular organelles that are known to produce energy through a process called oxidative phosphorylation. Besides their primary function, mitochondria are involved in various cellular processes, including cell growth, differentiation, signaling, metabolism, and senescence. Age-related changes cause a decline in mitochondrial quality and integrity due to increased mitochondrial mutations and oxidative damage. Thus, aging can severely impact mitochondrial functions,...
13.8K
Translocation of Proteins into the Mitochondria
3.1K
Mitochondrial precursors are translocated to the internal subcompartments via independent mechanisms involving distinct protein machineries called translocases.
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...
3.1K
Mitochondrial Precursor Proteins
2.6K
Mitochondrial precursors are partially unfolded or loosely folded polypeptide chains. Newly synthesized precursors are inhibited from spontaneously folding into their native conformation by the cytosolic chaperones, heat shock proteins 70 (Hsp70), and mitochondrial import stimulation factors (MSFs). Precursors bound to MSFs are guided to the TOM70-TOM37 receptors, while precursors bound to Hsp70 chaperones are targetted to TOM20-TOM22 receptor complexes.
Most of the mitochondrial...
Most of the mitochondrial...
2.6K
Electron Transport Chain: Complex I and II
14.5K
The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
ROS generation is regulated and maintained at moderate levels necessary...
14.5K
Mitochondrial Protein Sorting
4.4K
Mitochondria are double-membrane organelles of the eukaryotes involved in cellular metabolism, signaling, ATP synthesis, and programmed cell death. Each of these processes requires specific proteins and enzymes that must be correctly sorted to the right mitochondrial subcompartment for the proper functioning of the organelle.
Most of these mitochondrial proteins are encoded by the nucleus and imported to the mitochondria as unfolded or loosely folded precursors. Mitochondrial precursors...
Most of these mitochondrial proteins are encoded by the nucleus and imported to the mitochondria as unfolded or loosely folded precursors. Mitochondrial precursors...
4.4K
