USP7 Inhibition Promotes Early Osseointegration in Senile Osteoporotic Mice

IF 5.7 1区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
F. Zhou, Z. Wang, H. Li, D. Wang, Z. Wu, F. Bai, Q. Wang, W. Luo, G. Zhang, Y. Xiong, Y. Wu
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引用次数: 0

Abstract

Although elderly osteoporotic patients have similar implant survival rates compared with those of normal individuals, they require longer healing periods to achieve proper osseointegration. This may be related to chronic inflammatory responses and impaired stem cell repair functions in the osteoporotic bone microenvironment. Recently, the deubiquitinating enzyme, ubiquitin-specific peptidase 7 (USP7), was found to regulate the macrophage immune response and modulate stem cell osteogenic differentiation. The selective inhibitor of USP7, P5091, has also been found to promote bone repair and homeostasis in osteoporotic conditions. However, the roles of USP7 and P5091 in osteoimmunology and dental implant osseointegration under senile osteoporotic conditions remain unclear. In this study, USP7 depletion and P5091 were shown to inhibit inflammation in senescent bone marrow–derived macrophages (BMDMs) and promote osteogenic differentiation in aged bone marrow mesenchymal stromal cells (BMSCs). Furthermore, mRNA-Seq revealed that USP7 depletion could enhance efferocytosis in senescent BMDMs through the EPSIN1/low-density lipoprotein receptor-related protein 1 (LRP1) pathway and selectively induce apoptosis (senolysis) in aged BMSCs. In senile osteoporotic mice, we found that the osseointegration period was prolonged compared with young mice, and P5091 promoted the early stage of osseointegration, which may be related to macrophage efferocytosis around the implant. Collectively, this study suggests that USP7 inhibition may accelerate the osseointegration process in senile osteoporotic conditions by promoting macrophage efferocytosis and aged BMSCs apoptosis. This has implications for understanding the cellular interactions and signaling mechanisms in the peri-implant bone microenvironment under osteoporotic conditions. It may also provide clinical significance in developing new therapies to enhance osseointegration quality and shorten the edentulous period in elderly osteoporotic patients.
虽然老年骨质疏松症患者的植入物存活率与正常人相似,但他们需要更长的愈合期才能实现正常的骨结合。这可能与骨质疏松症骨微环境中的慢性炎症反应和干细胞修复功能受损有关。最近,研究发现去泛素化酶--泛素特异性肽酶7(USP7)可调节巨噬细胞免疫反应,并调节干细胞成骨分化。研究还发现,USP7 的选择性抑制剂 P5091 能促进骨质疏松情况下的骨修复和骨平衡。然而,USP7 和 P5091 在骨免疫学和老年性骨质疏松症条件下的牙种植体骨结合中的作用仍不清楚。本研究表明,USP7耗竭和P5091可抑制衰老骨髓源性巨噬细胞(BMDMs)的炎症反应,并促进衰老骨髓间充质基质细胞(BMSCs)的成骨分化。此外,mRNA-Seq 发现,USP7 的缺失可通过 EPSIN1/低密度脂蛋白受体相关蛋白 1(LRP1)途径增强衰老骨髓巨噬细胞的渗出,并选择性地诱导衰老骨髓间充质基质细胞的凋亡(衰老溶解)。在老年性骨质疏松症小鼠中,我们发现与年轻小鼠相比,骨结合时间延长,而 P5091 能促进骨结合的早期阶段,这可能与植入物周围巨噬细胞的渗出有关。综上所述,本研究表明,USP7抑制剂可通过促进巨噬细胞脱落和老化BMSCs凋亡来加速老年性骨质疏松症的骨结合过程。这对了解骨质疏松条件下种植体周围骨微环境中的细胞相互作用和信号转导机制具有重要意义。它还可能为开发新的疗法以提高骨结合质量和缩短老年骨质疏松症患者的无牙期提供临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Dental Research
Journal of Dental Research 医学-牙科与口腔外科
CiteScore
15.30
自引率
3.90%
发文量
155
审稿时长
3-8 weeks
期刊介绍: The Journal of Dental Research (JDR) is a peer-reviewed scientific journal committed to sharing new knowledge and information on all sciences related to dentistry and the oral cavity, covering health and disease. With monthly publications, JDR ensures timely communication of the latest research to the oral and dental community.
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