Bone Marrow Mesenchymal Stem Cell Senescence in the Development of Osteoporosis: Mechanisms, Interventions, and Future Directions.

IF 2.2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Chengen Li, Bo Li, Jiuchao Zhang, Kun Liu, Gang Du, Cunliang Guo, Zhenguo Yang
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Abstract

Osteoporosis, a significant age-related disease, is marked by diminished bone density and an elevated risk of fractures, representing a considerable global health challenge. Bone marrow mesenchymal stem cells (BMSCs) are essential in maintaining bone integrity through their differentiation into osteoblasts, which are crucial for bone formation. Nevertheless, the aging of BMSCs diminishes their regenerative abilities and intensifies inflammation, thereby playing a critical role in osteoporosis pathogenesis. This review explores the intricate mechanisms of BMSC senescence and its influence on osteoporosis, detailing cellular and molecular markers, such as oxidative stress, the senescence-associated secretory phenotype (SASP), and pivotal signaling pathways, including P53, PI3K/mTOR, and autophagy. We assess current interventions aimed at reducing BMSC senescence, with an emphasis on pharmacological methods like melatonin and antioxidants, alongside nonpharmacological strategies, such as exercise and dietary supplementation with omega-3 fatty acids. Furthermore, the challenges and limitations of translating these strategies into clinical applications are addressed, highlighting the necessity for personalized medicine to accommodate treatment outcome variability. Future research directions should focus on emerging therapeutic targets and novel interventions, such as gene editing technologies and advanced tissue engineering techniques. By integrating these strategies, this review endeavors to enhance the understanding and treatment of osteoporosis, emphasizing the critical need to target BMSC senescence to develop effective therapies.

骨质疏松症发展中的骨髓间充质干细胞衰老:机制、干预和未来方向。
骨质疏松症是一种与年龄有关的重大疾病,其特点是骨密度降低,骨折风险增加,是一项相当大的全球健康挑战。骨髓间充质干细胞(BMSCs)分化为成骨细胞,对维持骨完整性至关重要,成骨细胞是骨形成的关键。然而,骨髓间充质干细胞的老化降低了其再生能力并加剧了炎症,从而在骨质疏松的发病机制中发挥了关键作用。这篇综述探讨了BMSC衰老的复杂机制及其对骨质疏松症的影响,详细介绍了细胞和分子标记,如氧化应激、衰老相关分泌表型(SASP)和关键信号通路,包括P53、PI3K/mTOR和自噬。我们评估了目前旨在减少BMSC衰老的干预措施,重点是褪黑素和抗氧化剂等药物方法,以及非药物策略,如运动和补充omega-3脂肪酸。此外,解决了将这些策略转化为临床应用的挑战和局限性,强调了个性化医疗以适应治疗结果可变性的必要性。未来的研究方向应关注新兴的治疗靶点和新的干预措施,如基因编辑技术和先进的组织工程技术。通过整合这些策略,本综述努力提高对骨质疏松症的认识和治疗,强调针对BMSC衰老开发有效治疗的迫切需要。
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
Current molecular medicine
Current molecular medicine 医学-医学:研究与实验
CiteScore
5.00
自引率
4.00%
发文量
141
审稿时长
4-8 weeks
期刊介绍: Current Molecular Medicine is an interdisciplinary journal focused on providing the readership with current and comprehensive reviews/ mini-reviews, original research articles, short communications/letters and drug clinical trial studies on fundamental molecular mechanisms of disease pathogenesis, the development of molecular-diagnosis and/or novel approaches to rational treatment. The reviews should be of significant interest to basic researchers and clinical investigators in molecular medicine. Periodically the journal invites guest editors to devote an issue on a basic research area that shows promise to advance our understanding of the molecular mechanism(s) of a disease or has potential for clinical applications.
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