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骨髓间充质干细胞的年轻化:机制及其在老年性骨质疏松症治疗中的应用

Rejuvenation of Bone Marrow Mesenchymal Stem Cells: Mechanisms and Their Application in Senile Osteoporosis Treatment.

作者信息

Tian Rui-Chuan, Zhang Ru-Ya, Ma Chu-Fan

机构信息

Department of Stomatology, Air Force Medical Center, The Fourth Military Medical University, Beijing 100142, China.

Graduate School, China Medical University, Shenyang 110002, China .

出版信息

Biomolecules. 2025 Feb 13;15(2):276. doi: 10.3390/biom15020276.

DOI:10.3390/biom15020276
PMID:40001580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11853522/
Abstract

Bone marrow mesenchymal stromal cells (BM-MSCs) are multipotent cells present in bone marrow; they play a crucial role in the process of bone formation. Cellular senescence is defined as a stable state of cell cycle arrest that impairs the functioning of cells. Research has shown that aging triggers a state of senescence in BM-MSCs, leading to a reduced capacity for osteogenic differentiation and the accumulation of senescent cells, which can accelerate the onset of various diseases. Therefore, it is essential to explore mechanisms and strategies for the rejuvenation of senescent BM-MSCs. Senile osteoporosis (SOP) is a metabolic bone disease characterized by reduced bone formation. The senescence of BM-MSCs is considered one of the most important factors in the occurrence and development of SOP. Therefore, the rejuvenation of BM-MSCs for the treatment of SOP represents a promising strategy. This work provides a summary of the functional alterations observed in senescent BM-MSCs and a systematic review of the mechanisms that facilitate the rejuvenation of senescent BM-MSCs. Additionally, we analyze the progress in and the limitations associated with the application of rejuvenated senescent BM-MSCs to treat SOP, with the aim of providing new insights for the prevention and treatment of SOP.

摘要

骨髓间充质基质细胞(BM-MSCs)是存在于骨髓中的多能细胞;它们在骨形成过程中发挥着关键作用。细胞衰老被定义为一种稳定的细胞周期停滞状态,会损害细胞功能。研究表明,衰老会引发BM-MSCs的衰老状态,导致成骨分化能力降低和衰老细胞积累,进而加速各种疾病的发生。因此,探索衰老BM-MSCs年轻化的机制和策略至关重要。老年性骨质疏松症(SOP)是一种以骨形成减少为特征的代谢性骨病。BM-MSCs的衰老被认为是SOP发生和发展的最重要因素之一。因此,使BM-MSCs年轻化以治疗SOP是一种很有前景的策略。这项工作总结了衰老BM-MSCs中观察到的功能改变,并对促进衰老BM-MSCs年轻化的机制进行了系统综述。此外,我们分析了应用年轻化的衰老BM-MSCs治疗SOP的进展及相关局限性,旨在为SOP的预防和治疗提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/7e3fd71a97e0/biomolecules-15-00276-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/28a7f7577e4e/biomolecules-15-00276-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/236cbc2e8fab/biomolecules-15-00276-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/cd8822e3a6b8/biomolecules-15-00276-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/de84651176d4/biomolecules-15-00276-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/7e3fd71a97e0/biomolecules-15-00276-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/28a7f7577e4e/biomolecules-15-00276-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/236cbc2e8fab/biomolecules-15-00276-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/cd8822e3a6b8/biomolecules-15-00276-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/de84651176d4/biomolecules-15-00276-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94b9/11853522/7e3fd71a97e0/biomolecules-15-00276-g005.jpg

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1
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2
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Nature. 2024 Oct;634(8036):1150-1159. doi: 10.1038/s41586-024-07972-2. Epub 2024 Oct 2.
3
Inhibition of IL-11 signalling extends mammalian healthspan and lifespan.抑制 IL-11 信号转导可延长哺乳动物的健康寿命和寿命。
间充质干细胞、诱导多能干细胞和细胞外囊泡在人类肌肉骨骼组织修复中的应用:最终的成功是否取决于开发出优良的植入材料以及为植入创造最佳环境?这些选择的依据是什么?
Int J Mol Sci. 2025 Jun 28;26(13):6250. doi: 10.3390/ijms26136250.
Nature. 2024 Aug;632(8023):157-165. doi: 10.1038/s41586-024-07701-9. Epub 2024 Jul 17.
4
PPIA dictates NRF2 stability to promote lung cancer progression.PPIA 决定 NRF2 的稳定性以促进肺癌的进展。
Nat Commun. 2024 Jun 3;15(1):4703. doi: 10.1038/s41467-024-48364-4.
5
Accurate structure prediction of biomolecular interactions with AlphaFold 3.利用 AlphaFold 3 进行生物分子相互作用的精确结构预测。
Nature. 2024 Jun;630(8016):493-500. doi: 10.1038/s41586-024-07487-w. Epub 2024 May 8.
6
Targeting adipocyte ESRRA promotes osteogenesis and vascular formation in adipocyte-rich bone marrow.靶向脂肪细胞 ESRRA 可促进富含脂肪细胞的骨髓中的成骨和血管形成。
Nat Commun. 2024 May 4;15(1):3769. doi: 10.1038/s41467-024-48255-8.
7
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8
Lipids and lipid metabolism in cellular senescence: Emerging targets for age-related diseases.细胞衰老中的脂质和脂质代谢:与年龄相关疾病的新兴靶点。
Ageing Res Rev. 2024 Jun;97:102294. doi: 10.1016/j.arr.2024.102294. Epub 2024 Apr 5.
9
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J Cachexia Sarcopenia Muscle. 2024 Jun;15(3):934-948. doi: 10.1002/jcsm.13459. Epub 2024 Mar 29.
10
Targeting Cell Senescence and Senolytics: Novel Interventions for Age-Related Endocrine Dysfunction.靶向细胞衰老和衰老细胞清除:与年龄相关的内分泌功能障碍的新干预措施。
Endocr Rev. 2024 Sep 12;45(5):655-675. doi: 10.1210/endrev/bnae010.