Division of General Surgery, Department of Surgery, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Department of Physiology and Graduate Institute of Basic Medical Science, College of Medicine, China Medical University, Taichung, Taiwan.
J Orthop Res. 2019 Apr;37(4):942-947. doi: 10.1002/jor.24264. Epub 2019 Mar 28.
Expression of CCAAT/enhancer binding protein (C/EBP) homologous protein (CHOP) is induced during endoplasmic reticulum (ER) stress, which is related to apoptosis in several cell types. CHOP null mice have been exhibited to decrease bone formation. However, a study of transgenic mice overexpressing CHOP in the bone microenvironment showed that CHOP overexpression impairs the osteoblastic function leading to osteopenia. The regulatory role of CHOP in bone formation is controversial and still remains to be clarified. Here, we investigated the alterations in bone microstructure of CHOP knockout (Chop ) mice and tested the gender difference of CHOP deficiency in susceptibility to osteopenia. Adult female and male mice (WT) and Chop mice were used. The microcomputed tomography (µCT) analysis in trabecular bone and cortical bone of tibia was determined. Trabecular bone volume fraction (BV/TV), trabecular number, and bone mineral density (BMD) in tibia are markedly decreased in both male and female Chop mice compared to the control WT mice. Unexpectedly, the BMD and BV/TV in trabecular bone of tibia in female Chop mice were significantly lower than in male Chop mice. The similar results could also be observed in the cortical bone of tibia in Chop mice. This gender difference was also observed in the decreased capacity of osteoblast differentiation of bone marrow cells isolated from Chop mice. These results indicated that ER stress-related CHOP signaling might play an important role in the bone formation in a mouse model, especially in females. There is the gender difference of CHOP deficiency in susceptibility to osteopenia. © 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res.
CCAAT/增强子结合蛋白(C/EBP)同源蛋白(CHOP)的表达在内质网(ER)应激过程中被诱导,这与几种细胞类型的细胞凋亡有关。CHOP 基因敲除小鼠表现出骨形成减少。然而,一项在骨微环境中过表达 CHOP 的转基因小鼠研究表明,CHOP 过表达会损害成骨细胞功能,导致骨质疏松症。CHOP 在骨形成中的调节作用存在争议,仍有待阐明。在这里,我们研究了 CHOP 基因敲除(Chop )小鼠骨微结构的变化,并测试了 CHOP 缺乏对骨质疏松易感性的性别差异。使用成年雌性和雄性小鼠(WT)和 Chop 小鼠。对胫骨的小梁骨和皮质骨进行微计算机断层扫描(µCT)分析。与对照 WT 小鼠相比,雄性和雌性 Chop 小鼠的胫骨小梁骨体积分数(BV/TV)、小梁数和骨密度(BMD)均明显降低。出乎意料的是,雌性 Chop 小鼠胫骨小梁骨的 BMD 和 BV/TV 明显低于雄性 Chop 小鼠。在 Chop 小鼠的胫骨皮质骨中也可以观察到类似的结果。这种性别差异也存在于 Chop 小鼠骨髓细胞成骨分化能力下降的情况中。这些结果表明,与内质网应激相关的 CHOP 信号可能在小鼠模型的骨形成中发挥重要作用,尤其是在女性中。CHOP 缺乏对骨质疏松易感性存在性别差异。