4.7 Article

Mechanically induced autophagy is associated with ATP metabolism and cellular viability in osteocytes in vitro

Journal

REDOX BIOLOGY
Volume 14, Issue -, Pages 492-498

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.redox.2017.10.021

Keywords

Osteocyte; Fluid shear stress; Autophagy; ATP; Cell survival

Funding

  1. Fundamental Research Funds for the Central Universities in Chongqing University [CQDXWL-2012-126, CQDXWL-2013-026]
  2. Specialized Research Fund for the Doctoral Program of Higher Education of Chinese Ministry of Education [20110191120038]
  3. NIH [R01AR054385, P30GM103333]
  4. NSFC [11602046]
  5. Project Foundation of Chongqing Municipal Education Committee [KJ1600207]
  6. Chongqing Research Program of Basic Research and Frontier Technology [cstc2017jcyjAX0445]

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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.

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