Department of Oral and Maxillofacial Surgery, School & Hospital of Stomatology, Tongji University, Shanghai, China.
Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Shanghai, China.
J Cell Physiol. 2019 Jul;234(7):11165-11175. doi: 10.1002/jcp.27765. Epub 2018 Dec 12.
The rapid bone remodeling after osteotomy has been reported for a long time. However, the underlying mechanism promoting the active bone reconstruction was still to be elucidated. Since not only the bone, blood vessels, and supportive tissues, but also the local microenvironment were destroyed, if the changes on the cell metabolism was contributed to the accelerated bone remodeling came into sight. In present study, we found that the mandibular osteotomy in rabbit activated osteoclasts, as well as the expression of hypoxia-inducible factor 1α (HIF-1α) in alveolar bone. Hypoxia or HIF-1α could enhanced osteoclastogenesis, bone absorption, and lactic acid concentration in receptor activator of nuclear factor κΒ ligand-induced RAW264.7 cells. Coincided with the upregulated HIF-1α expression, HIF-driven glycolytic enzymes, such as lactate dehydrogenase A (LDHA), glucokinase (GCK), pyruvate kinase M2 (PKM2), and phosphofructokinase1 (PFK1), were found massively increased in both hypoxic RAW264.7 cells and the alveolar HIF-1α-positive osteoclasts after mandibular osteotomy. Knockdown of HIF-1α suppressed not only the hypoxia-mediated glycolysis, but also the hypoxia-induced acid secretion and bone resorption in RAW264.7 cells. Application of inhibitor on glycolysis gave rise to the similar results as HIF-1α knockdown. Our findings suggested that hypoxia-driven glycolysis in osteoclasts was an adaptive mechanism to permit alveolar bone remodeling after mandibular osteotomy.
骨切开术后的快速骨重塑已经被报道了很长时间。然而,促进活跃骨重建的潜在机制仍有待阐明。由于不仅骨骼、血管和支持组织,而且局部微环境都被破坏了,如果细胞代谢的变化有助于加速骨重塑,那么这一变化就会引起人们的关注。在本研究中,我们发现兔下颌骨切开术激活了破骨细胞,以及牙槽骨中缺氧诱导因子 1α(HIF-1α)的表达。缺氧或 HIF-1α 可以增强核因子κB 受体激活剂配体诱导的 RAW264.7 细胞中的破骨细胞生成、骨吸收和乳酸浓度。与 HIF-1α 表达上调一致,HIF 驱动的糖酵解酶,如乳酸脱氢酶 A(LDHA)、葡萄糖激酶(GCK)、丙酮酸激酶 M2(PKM2)和磷酸果糖激酶 1(PFK1),在缺氧 RAW264.7 细胞和下颌骨切开术后牙槽骨中 HIF-1α 阳性破骨细胞中大量增加。HIF-1α 的敲低不仅抑制了缺氧介导的糖酵解,也抑制了 RAW264.7 细胞中的缺氧诱导的酸分泌和骨吸收。糖酵解抑制剂的应用产生了与 HIF-1α 敲低相似的结果。我们的研究结果表明,破骨细胞中的缺氧驱动的糖酵解是允许下颌骨切开术后牙槽骨重塑的一种适应机制。