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骨硬化蛋白(SOST)在骨骼和骨外器官对机械刺激的反应中的作用。

Role of SOST in Response to Mechanical Stimulation in Bone and Extraosseous Organs.

作者信息

Chen Minyou, Li Wenjing, Lei Le, Zhang Lingli

机构信息

College of Athletic Performance, Shanghai University of Sport, Shanghai 200438, China.

School of Sport, Exercise and Health Sciences, Loughborough University, Loughborough LE11 3TU, UK.

出版信息

Biomolecules. 2025 Jun 11;15(6):856. doi: 10.3390/biom15060856.

DOI:10.3390/biom15060856
PMID:40563496
Abstract

Sclerostin (SOST) is a specific osteocyte protein. During the differentiation and proliferation of osteoblasts and osteoclasts, the high expression of SOST can inhibit bone formation and contribute to osteoporosis and the bone metastasis of malignant tumors. Most of the research on SOST has focused on bone cells, but studies have found that SOST is not a specific product of bone cells but that it is also expressed by articular chondrocytes. SOST can regulate the progression of osteoarthritis in bone and cartilage, promote subchondral bone sclerosis, and inhibit cartilage degeneration. A review of the literature found that SOST can not only regulate bone metabolism, but it is also expressed in cardiovascular, kidney, liver, and other tissues, influencing the occurrence and development of diseases in these organs and tissues. Studies have found that diseases of extra-bone organs, such as atherosclerosis, aneurysm, chronic kidney disease, and cirrhosis, may be related to the expression of SOST. Simultaneously, long-term exercise can reduce SOST levels, especially in areas of high bone strain. Prolonged exercise induces bone adaptation to mechanical stress, resulting in diminished responsiveness of bone cells to exercise and a reduction in serum SOST levels. Short-term acute exercise can elevate serum SOST levels, but these results are often limited by age, gender, and energy status. In general, serum SOST rises immediately after short-term acute exercise, returning to baseline or even decreasing after exercise.

摘要

硬化蛋白(SOST)是一种特定的骨细胞蛋白。在成骨细胞和破骨细胞的分化与增殖过程中,SOST的高表达会抑制骨形成,并导致骨质疏松和恶性肿瘤的骨转移。关于SOST的大多数研究都集中在骨细胞上,但研究发现SOST并非骨细胞的特异性产物,关节软骨细胞也可表达SOST。SOST能够调节骨与软骨中骨关节炎的进展,促进软骨下骨硬化,并抑制软骨退变。文献综述发现,SOST不仅能调节骨代谢,还在心血管、肾脏、肝脏等组织中表达,影响这些器官和组织疾病的发生与发展。研究发现,骨外器官的疾病,如动脉粥样硬化、动脉瘤、慢性肾病和肝硬化,可能与SOST的表达有关。同时,长期运动可降低SOST水平,尤其是在骨应变较高的部位。长时间运动可诱导骨骼适应机械应力,导致骨细胞对运动的反应性降低以及血清SOST水平下降。短期急性运动可使血清SOST水平升高,但这些结果常受年龄、性别和能量状态的限制。一般来说,短期急性运动后血清SOST会立即升高,运动后会恢复至基线水平甚至降低。

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本文引用的文献

1
Cardioprotective function of sclerostin by reducing calcium deposition, proliferation, and apoptosis in human vascular smooth muscle cells.骨硬化蛋白通过减少人血管平滑肌细胞中的钙沉积、增殖和凋亡发挥心脏保护作用。
Cardiovasc Diabetol. 2023 Nov 2;22(1):301. doi: 10.1186/s12933-023-02043-8.
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Elevated plasma sclerostin is associated with high brain amyloid-β load in cognitively normal older adults.血浆硬化蛋白水平升高与认知功能正常的老年人脑内高淀粉样蛋白β负荷相关。
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FGF-23 and sclerostin in serum and bone of CKD patients.
血清和骨组织中 CKD 患者的 FGF-23 和 Sclerostin。
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Associations of serum sclerostin levels with body composition, pulmonary function, and exacerbations in COPD patients.骨硬化蛋白水平与 COPD 患者的身体成分、肺功能和加重的相关性。
Pulmonology. 2024 Nov-Dec;30(6):512-521. doi: 10.1016/j.pulmoe.2022.06.003. Epub 2022 Aug 11.
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Sci Rep. 2022 Aug 4;12(1):13427. doi: 10.1038/s41598-022-17623-z.
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Importance of Sclerostin as Bone-Muscle Mediator Crosstalk.硬化蛋白作为骨-肌肉介质相互作用的重要性。
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Regulation of sclerostin by the SIRT1 stabilization pathway in osteocytes.成骨细胞中 SIRT1 稳定途径对骨硬化蛋白的调节。
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Endocrine Regulation of Extra-skeletal Organs by Bone-derived Secreted Protein and the effect of Mechanical Stimulation.骨源分泌蛋白对骨骼外器官的内分泌调节及机械刺激的作用
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Secreted Frizzled-Related Protein 5 Ameliorates Vascular Calcification in a Rat Model of Chronic Kidney Disease through the Wnt/β-Catenin Pathway.分泌型卷曲相关蛋白 5 通过 Wnt/β-连环蛋白通路减轻慢性肾脏病大鼠模型的血管钙化。
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