Stomatology Hospital, School of Stomatology, Zhejiang University School of Medicine, Zhejiang Provincial Clinical Research Center for Oral Diseases, Key Laboratory of Oral Biomedical Research of Zhejiang Province, Cancer Center of Zhejiang University, Engineering Research Center of Oral Biomaterials and Devices of Zhejiang Province, Hangzhou, Zhejiang Province 310000, China.
Zhejiang University School of Medicine, Hangzhou, Zhejiang Province 310000, China.
Bone. 2024 Oct;187:117172. doi: 10.1016/j.bone.2024.117172. Epub 2024 Jun 21.
Gain-of-function mutations in the low-density lipoprotein receptor-related protein 5 (LRP5) can cause high-bone-mass (HBM) phenotype, with 19 identified mutations so far. The A242T mutation in LRP5 has been found in 9 families, making it one of the most prevalent mutations. However, the correlation between the A242T mutation and HBM phenotype remains unverified in animal models. This study aimed to investigate the bone properties in a new transgenic mouse model carrying the LRP5 A241T missense mutation, equivalent to A242T in humans. Heterozygous Lrp5 mice were generated using CRISPR/Cas9 genome editing. Body weight increased with age from 4 to 16 weeks, higher in males than females, with no difference between Lrp5 mice and wild-type control. Micro-CT showed slightly longer femur and notably elevated trabecular bone mass of the femur and fifth lumbar spine with higher bone mineral density, bone volume fraction, and trabecular thickness in Lrp5 mice compared to wild-type mice. Additionally, increased cortical bone thickness and volume of the femur shaft and skull were observed in Lrp5 mice. Three-point bending tests of the tibia demonstrated enhanced bone strength properties in Lrp5 mice. Histomorphometry confirmed that the A241T mutation increased bone formation without affecting osteoblast number and reduced resorption activities in vivo. In vitro experiments indicated that the LRP5 A241T mutation enhanced osteogenic capacity of osteoblasts with upregulation of the Wnt signaling pathway, with no significant impact on the resorptive activity of osteoclasts. In summary, mice carrying the LRP5 A241T mutation displayed high bone mass and quality due to enhanced bone formation and reduced bone resorption in vivo, potentially mediated by the augmented osteogenic potential of osteoblasts. Continued investigation into the regulatory mechanisms of its bone metabolism and homeostasis may contribute to the advancement of novel therapeutic strategies for bone disorders.
LRP5 低密度脂蛋白受体相关蛋白 5 中的功能获得性突变可导致高骨量(HBM)表型,迄今为止已发现 19 种突变。LRP5 中的 A242T 突变已在 9 个家族中被发现,使其成为最常见的突变之一。然而,在动物模型中,LRP5 的 A242T 突变与 HBM 表型之间的相关性尚未得到验证。本研究旨在研究携带 LRP5 A241T 错义突变的新型转基因小鼠模型的骨骼特性,该突变与人的 A242T 突变等效。使用 CRISPR/Cas9 基因组编辑生成杂合 Lrp5 小鼠。从 4 到 16 周,体重随年龄增长而增加,雄性高于雌性,但 Lrp5 小鼠与野生型对照之间没有差异。微 CT 显示,Lrp5 小鼠的股骨略长,股骨和第五腰椎的小梁骨量显著升高,骨密度、骨体积分数和小梁厚度更高。此外,Lrp5 小鼠的股骨骨干和颅骨皮质骨厚度和体积增加。胫骨三点弯曲试验表明,Lrp5 小鼠的骨强度特性增强。组织形态计量学证实,A241T 突变增加了骨形成,而不影响成骨细胞数量,并减少了体内的吸收活动。体外实验表明,LRP5 A241T 突变增强了成骨细胞的成骨能力,上调了 Wnt 信号通路,对破骨细胞的吸收活性没有显著影响。总之,携带 LRP5 A241T 突变的小鼠由于体内骨形成增强和骨吸收减少而表现出高骨量和骨质量,这可能是由成骨细胞的成骨潜能增强介导的。对其骨代谢和平衡的调节机制的进一步研究可能有助于推进骨疾病的新型治疗策略。