Muscle Health Research Centre, Canada; School of Kinesiology and Health Science, York University, Toronto, Ontario, M3J 1P3, Canada.
Mol Metab. 2022 Dec;66:101623. doi: 10.1016/j.molmet.2022.101623. Epub 2022 Nov 1.
The Mitochondrial Unfolded Protein Response (UPR) is a compartment-specific mitochondrial quality control (MQC) mechanism that uses the transcription factor ATF5 to induce the expression of protective enzymes to restore mitochondrial function. Acute exercise is a stressor that has the potential to temporarily disrupt organellar protein homeostasis, however, the roles of ATF5 and the UPR in maintaining basal mitochondrial content, function and exercise-induced MQC mechanisms in skeletal muscle are not known.
ATF5 KO and WT mice were examined at rest or after a bout of acute endurance exercise. We measured protein content in whole muscle, nuclear, cytosolic and mitochondrial fractions, in addition to mRNA transcript levels in whole muscle. Using isolated mitochondria, we quantified rates of oxygen consumption and ROS emission to observe the effects of the absence of ATF5 on organelle function.
ATF5 KO mice exhibited a larger and less functional muscle mitochondrial pool, most likely a culmination of enhanced biogenesis via increased PGC-1α expression, and attenuated mitophagy. The absence of ATF5 resulted in a reduction in antioxidant proteins and increases in mitochondrial ROS emission, cytosolic cytochrome c, and the expression of mitochondrial chaperones. KO muscle also displayed enhanced exercise-induced stress kinase signaling, but a blunted mitophagic and UPR gene expression response, complemented by significant increases in the basal mRNA abundance and nuclear localization of ATF4. Instead of promoting its nuclear translocation, acute exercise caused the enrichment of ATF5 in mitochondrial fractions. We also identified PGC-1α as an additional regulator of the basal expression of UPR genes.
The transcription factor ATF5 retains a critical role in the maintenance of mitochondrial homeostasis and the appropriate response of muscle to acute exercise for the optimization of mitochondrial quality control.
线粒体未折叠蛋白反应(UPR)是一种特定于线粒体的质量控制(MQC)机制,它使用转录因子 ATF5 诱导保护性酶的表达,以恢复线粒体功能。急性运动是一种潜在的应激源,可能会暂时破坏细胞器蛋白质的动态平衡,然而,ATF5 和 UPR 在维持骨骼肌中基础线粒体含量、功能和运动诱导的 MQC 机制中的作用尚不清楚。
在休息或急性耐力运动后,我们检查了 ATF5 KO 和 WT 小鼠。我们测量了整个肌肉、核、胞质和线粒体部分的蛋白质含量,以及整个肌肉的 mRNA 转录水平。使用分离的线粒体,我们量化了耗氧率和 ROS 发射率,以观察 ATF5 缺失对细胞器功能的影响。
ATF5 KO 小鼠表现出更大和功能较差的肌肉线粒体池,这很可能是由于 PGC-1α 表达增加导致的增强的生物发生,以及减弱的线粒体自噬作用的结果。ATF5 的缺失导致抗氧化蛋白减少,线粒体 ROS 发射增加,胞质细胞色素 c 增加,以及线粒体伴侣蛋白的表达增加。KO 肌肉还显示出增强的运动诱导应激激酶信号,但线粒体自噬和 UPR 基因表达反应减弱,伴随着 ATF4 的基础 mRNA 丰度和核定位的显著增加。急性运动并没有促使 ATF5 向核内易位,而是导致 ATF5 在线粒体部分的富集。我们还发现 PGC-1α 是 UPR 基因基础表达的另一个调节剂。
转录因子 ATF5 在维持线粒体动态平衡和肌肉对急性运动的适当反应方面仍然起着关键作用,以优化线粒体质量控制。