Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing 400044, China.
Department of Medical Laboratory Technology, Institute of Life Sciences, Chongqing Medical University, Chongqing 400016, China.
Redox Biol. 2018 Apr;14:492-498. doi: 10.1016/j.redox.2017.10.021. Epub 2017 Nov 5.
Both mechanical loading and intracellular autophagy play important roles in bone homeostasis; however, their relationship remains largely unexplored. The objectives of this study were to determine whether osteocytes undergo autophagy upon fluid shear stress (FSS) loading and to determine the correlation between mechanically induced autophagy and ATP metabolism. Autophagic vacuoles were observed by transmission electron microscopy (TEM) in osteocyte-like MLO-Y4 cells subjected to FSS. Increased autophagic flux was further confirmed by the increased amount of the LC3-II isoform and the degradation of p62. Fluorescent puncta distributed in the cytoplasm were observed in the GFP-LC3 transformed cells subjected to FSS. Furthermore, FSS-induced ATP release and synthesis in osteocytes were attenuated by inhibiting autophagy with 3-MA. After FSS exposure, a high ratio of cell death was observed in cultures pretreated with 3-MA, an autophagy inhibitor, with no significantly different Caspase 3/7 activity. Our results indicated that FSS induces protective autophagy in osteocytes and that mechanically induced autophagy is associated with ATP metabolism and osteocyte survival. From the clinical perspective, it may be possible to enhance skeletal cell survival with drugs that modulate the autophagic state, and the autophagy-related pathway could be a potential target for the prevention of ageing-related bone disorders.
机械加载和细胞内自噬在骨稳态中都起着重要作用;然而,它们之间的关系在很大程度上仍未得到探索。本研究的目的是确定骨细胞在流体切应力(FSS)加载下是否会发生自噬,并确定机械诱导的自噬与 ATP 代谢之间的相关性。通过透射电子显微镜(TEM)观察到在 FSS 作用下的成骨细胞样 MLO-Y4 细胞中出现自噬小体。通过增加 LC3-II 同工型的量和 p62 的降解,进一步证实了自噬通量的增加。在 GFP-LC3 转化细胞中观察到在细胞质中分布的荧光斑点。此外,用 3-MA 抑制自噬可减弱 FSS 诱导的成骨细胞中 ATP 的释放和合成。在 FSS 暴露后,在用自噬抑制剂 3-MA 预处理的培养物中观察到高比例的细胞死亡,而 Caspase 3/7 活性没有明显差异。我们的结果表明,FSS 诱导成骨细胞中的保护性自噬,并且机械诱导的自噬与 ATP 代谢和骨细胞存活有关。从临床角度来看,用调节自噬状态的药物增强骨骼细胞的存活是可能的,并且自噬相关途径可能是预防与年龄相关的骨骼疾病的潜在靶点。