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激活的 FGFR3 抑制去卵巢小鼠模型中的骨再生和骨矿化。

Activated FGFR3 suppresses bone regeneration and bone mineralization in an ovariectomized mouse model.

机构信息

Department of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, 4668550, Nagoya, Aichi, Japan.

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, 4668550, Nagoya, Aichi, Japan.

出版信息

BMC Musculoskelet Disord. 2023 Mar 16;24(1):200. doi: 10.1186/s12891-023-06318-9.

Abstract

BACKGROUND

Postmenopausal osteoporosis is a widespread health concern due to its prevalence among older adults and an associated high risk of fracture. The downregulation of bone regeneration delays fracture healing. Activated fibroblast growth factor receptor 3 (FGFR3) accelerates bone regeneration at juvenile age and downregulates bone mineralization at all ages. However, the impact of FGFR3 signaling on bone regeneration and bone mineralization post-menopause is still unknown. This study aimed to evaluate the impact of FGFR3 signaling on bone regeneration and bone mineralization during menopause by developing a distraction osteogenesis (DO) mouse model after ovariectomy (OVX) using transgenic mice with activated FGFR3 driven by Col2a1 promoter (Fgfr3 mice).

METHODS

The OVX or sham operations were performed in 8-week-old female Fgfr3 and wild-type mice. After 8 weeks of OVX surgery, DO surgery in the lower limb was performed. The 5-day-latency period followed by performing distraction for 9 days. Bone mineral density (BMD) and bone regeneration was assessed by micro-computed tomography (micro-CT) scan and soft X-ray. Bone volume in the distraction area was also evaluated by histological analysis after 7 days at the end of distraction. Osteogenic differentiation and mineralization of bone marrow-derived mesenchymal stem cells (BMSCs) derived from each mouse after 8 weeks of the OVX or sham operations were also evaluated with and without an inhibitor for FGFR3 signaling (meclozine).

RESULTS

BMD decreased after OVX in both groups, and it further deteriorated in Fgfr3 mice. Poor callus formation after DO was also observed in both groups with OVX, and the amount of regenerated bone was further decreased in Fgfr3 mice. Similarly, histological analysis revealed that Fgfr3 OVX mice showed lower bone volume. Osteogenic differentiation and mineralization of BMSCs were also deteriorated in Fgfr3 OVX mice. An inhibitor for FGFR3 signaling dramatically reversed the inhibitory effect of OVX and FGFR3 signaling on BMSC mineralization.

CONCLUSION

Upregulated FGFR3 decreased newly regenerated bone after DO and BMD in OVX mice. FGFR3 signaling can be a potential therapeutic target in patients with postmenopausal osteoporosis.

摘要

背景

绝经后骨质疏松症是老年人中普遍存在的健康问题,且与骨折风险增加有关。骨再生的下调会延迟骨折愈合。激活的成纤维细胞生长因子受体 3(FGFR3)可加速青少年时期的骨再生,并在所有年龄段下调骨矿化。然而,FGFR3 信号对绝经后骨再生和骨矿化的影响仍不清楚。本研究旨在通过使用 Col2a1 启动子驱动 FGFR3 激活的转基因小鼠(Fgfr3 小鼠)建立去卵巢(OVX)后牵张成骨(DO)小鼠模型,评估 FGFR3 信号对绝经后骨再生和骨矿化的影响。

方法

在 8 周龄的 Fgfr3 和野生型雌性小鼠中进行 OVX 或假手术。OVX 手术后 8 周,行下肢 DO 手术。5 天潜伏期后,行 9 天牵张。通过 micro-CT 扫描和软 X 射线评估骨密度(BMD)和骨再生。牵张结束后 7 天,通过组织学分析评估牵张区的骨体积。还评估了 OVX 或假手术后 8 周来自每个小鼠的骨髓间充质干细胞(BMSC)的成骨分化和矿化情况,同时还评估了 FGFR3 信号抑制剂(美克洛嗪)的作用。

结果

两组小鼠 OVX 后 BMD 均下降,Fgfr3 小鼠进一步恶化。两组 OVX 后 DO 后均可见骨痂形成不良,Fgfr3 小鼠再生骨量进一步减少。同样,组织学分析显示 Fgfr3 OVX 小鼠的骨体积较低。Fgfr3 OVX 小鼠的 BMSC 成骨分化和矿化也恶化。FGFR3 信号抑制剂可显著逆转 OVX 和 FGFR3 信号对 BMSC 矿化的抑制作用。

结论

上调的 FGFR3 减少了 OVX 小鼠 DO 后新再生骨和 BMD。FGFR3 信号可能是绝经后骨质疏松症患者的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6389/10018961/29c7e745da79/12891_2023_6318_Fig1_HTML.jpg

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