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1. 西南医科大学附属口腔医院 正畸科,泸州,646000
2. 四川大学华西口腔医院 唇腭裂外科,成都,610041
纸质出版日期:2024,
网络出版日期:2024-1-20,
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范智博, 魏绵兴, 李胜鸿, 等. 低氧条件下HIF-1α对骨生理中成骨和破骨的影响[J]. 西南医科大学学报, 2024,47(1):80-86.
Effects of HIF-1α on osteogenesis and osteoblastogenesis in bone physiology under hypoxic conditions[J]. Journal of Southwest Medical University, 2024,47(1):80-86.
范智博, 魏绵兴, 李胜鸿, 等. 低氧条件下HIF-1α对骨生理中成骨和破骨的影响[J]. 西南医科大学学报, 2024,47(1):80-86. DOI: 10.3969/j.issn.2096-3351.2024.01.016.
Effects of HIF-1α on osteogenesis and osteoblastogenesis in bone physiology under hypoxic conditions[J]. Journal of Southwest Medical University, 2024,47(1):80-86. DOI: 10.3969/j.issn.2096-3351.2024.01.016.
骨的吸收、生成及稳态的维持是建立在成骨和破骨事件基础上的,上述这些过程是由多种因子共同参与调控。其中缺氧诱导因子-1α(hypoxia inducible factor-1α
HIF-1α)作为低氧的标志物,已被证实参与了多种成骨及破骨过程。各种体内外低氧模型也提供了HIF-1α直接或间接调控成骨及破骨过程的相关证据,但其对成骨及破骨的影响及机制并未得到系统性总结。所以本文对HIF-1α参与成骨、破骨的调控机制及其所涉及的相关临床事件进行了综述。总的来说,低氧条件下HIF-1α主要是通过与成骨及破骨相关基因的缺氧反应元件(hypoxia response element,HRE)结合从而直接参与成骨及破骨过程。除此之外,HIF-1α还可以通过增强糖酵解从而维持成骨及破骨能量的需求,但与此同时酸化的环境会进一步刺激破骨的产生。通过文献回顾,我们发现低氧条件下HIF-1α调控的成骨及破骨两种不同事件可能与低氧的持续时间和浓度有着密切联系,而不同氧条件下所导致的糖酵解的酸化程度可能是决定HIF-1α介导成骨和破骨走向的关键因素。低氧持续时间作为“低氧剂量”的一个组成部分对骨生理反应有着重要影响,同时其激发的HIF亚型转化这一现象对骨生理的影响也至关重要。据此本文通过对低氧下HIF-1α在成骨破骨进程的调控作用进行综述,以期为低氧下骨生理调控的相关机制提供一定的理论参考。
Bone resorption
formation and homeostasis maintenance are based on osteogenic and osteoclastic phenomenon
which include the regulation of a variety of factors. HIF-1α
as a marker of hypoxia
has been confirmed participating in a variety of process related to osteogenesis and osteoclast. And various vivo and in vitro hypoxia models have further revealed that HIF-1α can regulate bone physiology. These studies provide direct or indirect evidence that HIF-1α regulates osteogenic and osteoclastic events
but the effects of HIF-1α on osteogenesis and osteoclasty have not been systematically summarized. This review summarized the mechanism of regulation of HIF-1α on osteogenesis and osteoclasty and its participation in relevant clinical events. HIF-1α directly participates in osteogenesis and osteoclasty mainly through combing with the hypoxia response element (HRE) of osteogenesis related gene and osteoclast related gene under hypoxia. In addition
HIF-1α can also achieve the energy demand of osteogenic and osteoclastic events by enhancing glycolysis. But at the same time
the acidified environment will further stimulate the actvition of osteoclasts. Through the above review
we found that the two different events of osteogenesis and osteoclast regulated by HIF-1α may be closely related to the duration and concentration of hypoxia
and the acidification degree of glycolysis under different oxygen conditions
mediated by HIF-1α
may be the key factors that determine the trend of osteogenesis and osteoclast. We believe that hypoxia duration
as a part of "hypoxia dose"
should have an important impact on bone physiology
which needs more attention in future research. At the same time
in the state of continuous hypoxia
the transformation of HIF subtypes is also worthy of more in-depth study on the impact of bone physiology.Therefore
this article focuses on the effect of HIF-1αon osteogenesis and osteoclasis process under hypoxia
and provide a theoretical basis for the regulation mechanisms of bone physiological changes under hypoxia.
低氧缺氧诱导因子-1α成骨破骨
HypoxiaHIF-1αOsteogenesisOsteoclastic
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