Cartilage-Specific Autophagy Deficiency Promotes ER Stress and Impairs Chondrogenesis in PERK-ATF4-CHOP–Dependent Manner

Mar 18, 2017Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Lack of Cell Recycling in Cartilage Increases Stress in Protein Folding and Hurts Cartilage Formation Through the PERK-ATF4-CHOP Pathway

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Abstract

Atg7cKO mice exhibited growth retardation associated with reduced chondrocyte proliferation and differentiation.

  • Autophagy is activated during nutrient deprivation and low oxygen conditions to support cell survival.
  • Growth plate chondrocytes with Atg7 ablation showed increased cell death and signs of endoplasmic reticulum stress.
  • The PERK-ATF4-CHOP pathway was primarily activated in response to autophagy deficiency in growth plate chondrocytes.
  • Chemical chaperone phenylbutyric acid (PBA) partially mitigated the negative effects of autophagy loss on bone growth.
  • Defective autophagy in cultured chondrocytes led to decreased proliferation and differentiation markers, alongside increased apoptosis.

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