Shanghai Jiaotong Daxue xuebao. Yixue ban (Jun 2024)

Generation and validation of the conditional osteoblast-specific retinoic acid signaling inhibition mouse model

  • SUN Siyuan,
  • LIU Yuanqi,
  • CUI Yiwen,
  • HUANG Zihan,
  • MEI Li,
  • DAI Qinggang,
  • JIANG Lingyong

DOI
https://doi.org/10.3969/j.issn.1674-8115.2024.06.002
Journal volume & issue
Vol. 44, no. 6
pp. 676 – 686

Abstract

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Objective·To construct and verify the mouse model that can mimic the vitamin A deficiency (VAD)-like craniofacial skeletal deformity and do not cause embryonic death.Methods·Based on the Cre-LoxP system, the OsxCre;Rosa26dn/dn mice expressing osteoblast-specific dominant-negative retinoid acid receptor α (dnRARα) mutation were obtained by hybridization through OsxCre and Rosa26dnRARα/dnRARα mice, to achieve the conditional inhibition of retinoic acid signaling to simulate VAD disease. Femur bone mesenchymal stem cells (BMSCs) and parietal bone cells of OsxCre;Rosa26dn/dn mice and their control littermates were isolated and underwent osteogenic induction, to assess the expression of retinoid acid receptor α (RARα) protein through Western blotting. Osteoblasts induced from parietal bone cells of OsxCre;Rosa26dn/dn mice and their control littermates were isolated and the effect of retinoic acid signaling inhibition was verified through dual luciferase gene reporter assay. Meanwhile, Ad-eGFP or Ad-Cre adenovirus-infected femur BMSCs and parietal bone cells of Rosa26dn/dn mice underwent osteogenic induction to assess the expression of dominant-negative mutant protein and the inhibition of the retinoic acid signaling pathway in vitro by Western blotting and dual luciferase gene reporter assay. Moreover, the skulls of 6-week-old OsxCre;Rosa26dn/dn mice were collected, and Micro-CT scanning and three-dimensional (3D) reconstruction were performed to verify the craniofacial skeletal deformities of the mouse model.Results·Western blotting results demonstrated that the level of RARα protein increased in the femur and parietal osteoblasts of OsxCre;Rosa26dn/dn mice compared to that of their control littermates, and also increased in the Ad-Cre-infected femur and parietal osteoblasts of Rosa26dn/dn mice compared to that in the Ad-eGFP-infected group (P<0.05). Dual luciferase gene reporter assay results indicated that the activity of retinoid acid response element (RARE) was inhibited in the osteoblasts of OsxCre;Rosa26dn/dn mice compared to their control littermates, and was also inhibited in the Ad-Cre-infected group compared to the Ad-eGFP-infected group (P<0.05). Micro-CT and 3D reconstruction suggested that the skull of 6-week-old OsxCre;Rosa26dn/dn mice exhibited VAD-like craniofacial skeletal deformities, including smaller size of the skull and osteogenesis imperfecta compared to their control littermates.Conclusion·An osteoblast-specific dnRARα expressing mouse model that can mimic VAD-like craniofacial skeletal deformity is successfully constructed, therefore providing a new model for exploring the pathogenesis and therapeutic targets of VAD-like craniofacial skeletal deformity in the future.

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