Edman Sebastian, Flockhart Mikael, Larsen Filip J, Apró William
Department of Women's and Children's Health, Karolinska Institute, Stockholm, Sweden; The Åstrand Laboratory, Department of Physiology, Nutrition and Biomechanics, The Swedish School of Sport and Health Sciences, Stockholm, Sweden.
The Åstrand Laboratory, Department of Physiology, Nutrition and Biomechanics, The Swedish School of Sport and Health Sciences, Stockholm, Sweden; Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
Mol Metab. 2024 Jan;79:101854. doi: 10.1016/j.molmet.2023.101854. Epub 2023 Dec 15.
Human skeletal muscle consists of a mixture of slow- and fast-twitch fibers with distinct capacities for contraction mechanics, fermentation, and oxidative phosphorylation. While the divergence in mitochondrial volume favoring slow-twitch fibers is well established, data on the fiber type-specific intrinsic mitochondrial function and morphology are highly limited with existing data mainly being generated in animal models. This highlights the need for more human data on the topic.
Here, we utilized THRIFTY, a rapid fiber type identification protocol to detect, sort, and pool fast- and slow-twitch fibers within 6 h of muscle biopsy sampling. Respiration of permeabilized fast- and slow-twitch fiber pools was then analyzed with high-resolution respirometry. Using standardized western blot procedures, muscle fiber pools were subsequently analyzed for control proteins and key proteins related to respiratory capacity.
Maximal complex I+II respiration was 25% higher in human slow-twitch fibers compared to fast-twitch fibers. However, per mitochondrial volume, the respiratory rate of mitochondria in fast-twitch fibers was approximately 50% higher for complex I+II, which was primarily mediated through elevated complex II respiration. Furthermore, the abundance of complex II protein and proteins regulating cristae structure were disproportionally elevated in mitochondria of the fast-twitch fibers. The difference in intrinsic respiratory rate was not reflected in fatty acid-or complex I respiration.
Mitochondria of human fast-twitch muscle fibers compensate for their lack of volume by substantially elevating intrinsic respiratory rate through increased reliance on complex II.
人类骨骼肌由慢肌纤维和快肌纤维混合组成,它们在收缩力学、发酵和氧化磷酸化方面具有不同的能力。虽然线粒体体积偏向慢肌纤维的差异已得到充分证实,但关于纤维类型特异性内在线粒体功能和形态的数据非常有限,现有数据主要来自动物模型。这凸显了在该主题上需要更多人类数据。
在此,我们利用THRIFTY,一种快速纤维类型鉴定方案,在肌肉活检采样后6小时内检测、分选并汇集快肌纤维和慢肌纤维。然后用高分辨率呼吸测定法分析通透的快肌纤维和慢肌纤维池的呼吸作用。随后,使用标准化的蛋白质免疫印迹程序,对肌肉纤维池中的对照蛋白和与呼吸能力相关的关键蛋白进行分析。
与快肌纤维相比,人类慢肌纤维中最大的复合体I + II呼吸作用高25%。然而,按线粒体体积计算,快肌纤维中线粒体的复合体I + II呼吸速率大约高50%,这主要是通过提高复合体II的呼吸作用介导的。此外,快肌纤维线粒体中复合体II蛋白和调节嵴结构的蛋白丰度不成比例地升高。内在呼吸速率的差异在脂肪酸或复合体I呼吸中未体现。
人类快肌纤维的线粒体通过增加对复合体II的依赖,大幅提高内在呼吸速率,以弥补其体积上的不足。