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1. Laboratory of Developmental Biology, Department of Cell Biology and Genetics, School of Basic Medical Science, Chongqing Medical University,Chongqing,China,400016
2. Laboratory of Stem Cells and Tissue Engineering, School of Basic Medical Science, Chongqing Medical University,Chongqing,China,400016
3. Department of Orthopedics, The 1st Affiliated Hospital of Chongqing Medical University,Chongqing,China,400016
4. Department of Wound Repair and Rehabilitation Medicine, State Key Laboratory of Trauma, Burns and Combined Injury, Trauma Center, Research Institute of Surgery, Daping Hospital, Army Medical University,Chongqing,China,400042
纸质出版日期:2024,
网络出版日期:2024-1-1,
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IRE1α regulates the PTHrP-IHH feedback loop to orchestrate chondrocyte hypertrophy and cartilage mineralization[J]. Genes & Diseases, 2024,1(1):464-478.
Mengtian Fan, Nana Geng, Xingyue Li, et al. IRE1α regulates the PTHrP-IHH feedback loop to orchestrate chondrocyte hypertrophy and cartilage mineralization[J]. Genes & Diseases, 2024,1(1):464-478.
IRE1α regulates the PTHrP-IHH feedback loop to orchestrate chondrocyte hypertrophy and cartilage mineralization[J]. Genes & Diseases, 2024,1(1):464-478. DOI: 10.1016/j.gendis.2022.11.021.
Mengtian Fan, Nana Geng, Xingyue Li, et al. IRE1α regulates the PTHrP-IHH feedback loop to orchestrate chondrocyte hypertrophy and cartilage mineralization[J]. Genes & Diseases, 2024,1(1):464-478. DOI: 10.1016/j.gendis.2022.11.021.
Cartilage development is controlled by the highly synergistic proliferation and differentiation of growth plate chondrocytes
in which the Indian hedgehog (IHH) and parathyroid hormone-related protein-parathyroid hormone-1 receptor (PTHrP-PTH1R) feedback loop is crucial. The inositol-requiring enzyme 1α/X-box-binding protein-1 spliced (IRE1α/XBP1s) branch of the unfolded protein response (UPR) is essential for normal cartilage development. However
the precise role of ER stress effector IRE1α
encoded by endoplasmic reticulum to nucleus signaling 1 (
ERN1
)
in skeletal development remains unknown. Herein
we reported that loss of IRE1α accelerates chondrocyte hypertrophy and promotes endochondral bone growth.
ERN1
acts as a negative regulator of chondrocyte proliferation and differentiation in postnatal growth plates. Its deficiency interrupted PTHrP/PTH1R and IHH homeostasis leading to impaired chondrocyte hypertrophy and differentiation.
XBP1s
produced by p-IRE1α-mediated splicing
binds and up-regulates PTH1R and IHH
which coordinate cartilage development. Meanwhile
ER stress cannot be activated normally in
ERN1
-deficient chondrocytes. In conclusion
ERN1
deficiency accelerates chondrocyte hypertrophy and cartilage mineralization by impairing the homeostasis of the IHH and PTHrP/PTH1R feedback loop and ER stress.
ERN1
may have a potential role as a new target for cartilage growth and maturation.
Cartilage developmentER stressERN1IHHPTHrP/PTH1R
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