Department of Cell Biology, Histology and Pharmacology, Faculty of Medicine, University of Valladolid, 47003 Valladolid, Spain.
IOBA, University of Valladolid, 47011 Valladolid, Spain.
Int J Mol Sci. 2022 Mar 17;23(6):3233. doi: 10.3390/ijms23063233.
Bone is crucial for the support of muscles and the protection of vital organs, and as a reservoir of calcium and phosphorus. Bone is one of the most metabolically active tissues and is continuously renewed to adapt to the changes required for healthy functioning. To maintain normal cellular and physiological bone functions sufficient oxygen is required, as evidence has shown that hypoxia may influence bone health. In this scenario, this review aimed to analyze the molecular mechanisms involved in hypoxia-induced bone remodeling alterations and their possible clinical consequences. Hypoxia has been associated with reduced bone formation and reduced osteoblast matrix mineralization due to the hypoxia environment inhibiting osteoblast differentiation. A hypoxic environment is involved with increased osteoclastogenesis and increased bone resorptive capacity of the osteoclasts. Clinical studies, although with contradictory results, have shown that hypoxia can modify bone remodeling.
骨骼对于肌肉的支撑和重要器官的保护至关重要,同时也是钙和磷的储存库。骨骼是新陈代谢最活跃的组织之一,为了适应健康功能所需的变化,骨骼会不断更新。为了维持正常的细胞和生理骨骼功能,需要有足够的氧气,因为有证据表明,缺氧可能会影响骨骼健康。在这种情况下,本综述旨在分析缺氧诱导的骨骼重塑改变所涉及的分子机制及其可能的临床后果。由于缺氧环境抑制成骨细胞分化,缺氧与骨形成减少和成骨细胞基质矿化减少有关。缺氧环境与破骨细胞生成增加和破骨细胞的骨吸收能力增强有关。临床研究虽然结果相互矛盾,但表明缺氧可以改变骨重塑。