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衰老相关分泌表型在骨质流失中的作用。

The Role of Senescence-Associated Secretory Phenotype in Bone Loss.

作者信息

Zhu Runjiu, Wan Haoyang, Yang Hong, Song Mingrui, Chai Yu, Yu Bin

机构信息

Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Guangdong Provincial Key Laboratory of Bone and Cartilage Regenerative Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, China.

出版信息

Front Cell Dev Biol. 2022 Feb 9;10:841612. doi: 10.3389/fcell.2022.841612. eCollection 2022.

DOI:10.3389/fcell.2022.841612
PMID:35223858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8864518/
Abstract

As the population of most nations have a large proportion of older individuals, there is an increase in the prevalence of osteoporosis. Consequently, scientists have focused their attention on the pathogenic mechanisms of osteoporosis. Owing to an increase in studies on cellular senescence in recent years, research has begun to focus on the function of the senescent microenvironment in osteoporosis. With chronic inflammation, senescent cells in the bone marrow secrete a series of factors known as senescence-associated secretory phenotype (SASP) factors, acting on their own or surrounding healthy cells and consequently exacerbating ageing.The components of the SASP may differ depending on the cause of osteoporosis. This review aimed to summarize the relationship between SASP factors and osteoporosis and suggest new insights into the mechanistic investigation of osteoporosis.

摘要

由于大多数国家的人口中老年人占比很大,骨质疏松症的患病率有所上升。因此,科学家们将注意力集中在骨质疏松症的致病机制上。近年来,随着对细胞衰老研究的增加,研究开始关注衰老微环境在骨质疏松症中的作用。在慢性炎症的情况下,骨髓中的衰老细胞会分泌一系列称为衰老相关分泌表型(SASP)因子的物质,这些因子会作用于自身或周围的健康细胞,从而加剧衰老。SASP的成分可能因骨质疏松症的病因不同而有所差异。本综述旨在总结SASP因子与骨质疏松症之间的关系,并为骨质疏松症的机制研究提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/040d/8864518/f2c769ec3779/fcell-10-841612-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/040d/8864518/f2c769ec3779/fcell-10-841612-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/040d/8864518/f2c769ec3779/fcell-10-841612-g001.jpg

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Adv Sci (Weinh). 2022 Jan;9(1):e2104128. doi: 10.1002/advs.202104128. Epub 2021 Nov 5.
2
Senescent immune cells release grancalcin to promote skeletal aging.衰老免疫细胞释放粒酶来促进骨骼衰老。
Cell Metab. 2021 Oct 5;33(10):1957-1973.e6. doi: 10.1016/j.cmet.2021.08.009. Epub 2021 Sep 9.
3
Radiation-Induced Osteocyte Senescence Alters Bone Marrow Mesenchymal Stem Cell Differentiation Potential via Paracrine Signaling.
CNS Neurosci Ther. 2024 Oct;30(10):e70053. doi: 10.1111/cns.70053.
4
Inflammatory Processes Affecting Bone Health and Repair.炎症过程对骨骼健康和修复的影响。
Curr Osteoporos Rep. 2023 Dec;21(6):842-853. doi: 10.1007/s11914-023-00824-4. Epub 2023 Sep 28.
5
The Ins and Outs of Endosteal Niche Disruption in the Bone Marrow: Relevance for Myeloma Oncogenesis.骨髓中骨内膜龛破坏的来龙去脉:与骨髓瘤发生的相关性
Biology (Basel). 2023 Jul 12;12(7):990. doi: 10.3390/biology12070990.
6
Circulating Monocytes Act as a Common Trigger for the Calcification Paradox of Osteoporosis and Carotid Atherosclerosis TGFB1-SP1 and TNFSF10-NFKB1 Axis.循环单核细胞作为骨质疏松症和颈动脉粥样硬化钙化悖论的共同触发因素 TGFB1-SP1 和 TNFSF10-NFKB1 轴。
Front Endocrinol (Lausanne). 2022 Jul 22;13:944751. doi: 10.3389/fendo.2022.944751. eCollection 2022.
辐射诱导破骨细胞衰老通过旁分泌信号改变骨髓间充质干细胞的分化潜能。
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4
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5
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Cell Rep. 2021 Jul 20;36(3):109419. doi: 10.1016/j.celrep.2021.109419.
6
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7
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Front Immunol. 2021 Mar 4;12:631821. doi: 10.3389/fimmu.2021.631821. eCollection 2021.
8
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Cell Stem Cell. 2021 Jun 3;28(6):1057-1073.e7. doi: 10.1016/j.stem.2021.01.010. Epub 2021 Feb 10.
9
Pathological angiogenesis in retinopathy engages cellular senescence and is amenable to therapeutic elimination via BCL-xL inhibition.视网膜病变中的病理性血管生成涉及细胞衰老,并且可以通过 BCL-xL 抑制进行治疗性消除。
Cell Metab. 2021 Apr 6;33(4):818-832.e7. doi: 10.1016/j.cmet.2021.01.011. Epub 2021 Feb 5.
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