College of Life Sciences, Nankai University, Tianjin 300071, China.
Department of Biochemistry, Rush University Medical Center, Chicago, IL 60612.
J Bone Miner Res. 2013 Sep;28(9):1870-1884. doi: 10.1002/jbmr.1958.
Activating transcription factor 4 (ATF4) is a critical transcription factor for bone remodeling; however, its role in bone angiogenesis has not been established. Here we show that ablation of the Atf4 gene expression in mice severely impaired skeletal vasculature and reduced microvascular density of the bone associated with dramatically decreased expression of hypoxia-inducible factor 1α (HIF-1α) and vascular endothelial growth factor (VEGF) in osteoblasts located on bone surfaces. Results from in vivo studies revealed that hypoxia/reoxygenation induction of HIF-1α and VEGF expression leading to bone angiogenesis, a key adaptive response to hypoxic conditions, was severely compromised in mice lacking the Atf4 gene. Loss of ATF4 completely prevented endothelial sprouting from embryonic metatarsals, which was restored by addition of recombinant human VEGF protein. In vitro studies revealed that ATF4 promotion of HIF-1α and VEGF expression in osteoblasts was highly dependent upon the presence of hypoxia. ATF4 interacted with HIF-1α in hypoxic osteoblasts, and loss of ATF4 increased HIF-1α ubiquitination and reduced its protein stability without affecting HIF-1α mRNA stability and protein translation. Loss of ATF4 increased the binding of HIF-1α to prolyl hydroxylases, the enzymes that hydroxylate HIF-1a protein and promote its proteasomal degradation via the pVHL pathway. Furthermore, parathyroid hormone-related protein (PTHrP) and receptor activator of NF-κB ligand (RANKL), both well-known activators of osteoclasts, increased release of VEGF from the bone matrix and promoted angiogenesis through the protein kinase C- and ATF4-dependent activation of osteoclast differentiation and bone resorption. Thus, ATF4 is a new key regulator of the HIF/VEGF axis in osteoblasts in response to hypoxia and of VEGF release from bone matrix, two critical steps for bone angiogenesis.
激活转录因子 4(ATF4)是骨重塑的关键转录因子;然而,其在骨血管生成中的作用尚未确定。在这里,我们显示在小鼠中敲除 Atf4 基因表达严重损害了骨骼脉管系统,并降低了与骨表面成骨细胞中缺氧诱导因子 1α(HIF-1α)和血管内皮生长因子(VEGF)表达显著降低相关的微血管密度。体内研究结果表明,缺氧/复氧诱导的 HIF-1α 和 VEGF 表达导致骨血管生成,这是对缺氧条件的关键适应性反应,在缺乏 Atf4 基因的小鼠中受到严重损害。ATF4 的缺失完全阻止了来自胚胎跖骨的内皮芽生,而添加重组人 VEGF 蛋白可恢复内皮芽生。体外研究表明,ATF4 在成骨细胞中促进 HIF-1α 和 VEGF 表达高度依赖于缺氧的存在。在缺氧的成骨细胞中,ATF4 与 HIF-1α 相互作用,而 ATF4 的缺失增加了 HIF-1α 的泛素化,并降低了其蛋白质稳定性,而不影响 HIF-1α mRNA 稳定性和蛋白质翻译。ATF4 的缺失增加了 HIF-1α 与脯氨酰羟化酶的结合,脯氨酰羟化酶是羟化 HIF-1a 蛋白并通过 pVHL 途径促进其蛋白酶体降解的酶。此外,甲状旁腺激素相关蛋白(PTHrP)和核因子-κB 受体激活剂配体(RANKL),这两种已知的破骨细胞激活剂,增加了骨基质中 VEGF 的释放,并通过蛋白激酶 C 和 ATF4 依赖的破骨细胞分化和骨吸收的激活促进血管生成。因此,ATF4 是成骨细胞中缺氧反应和骨基质中 VEGF 释放的 HIF/VEGF 轴的新的关键调节剂,这是骨血管生成的两个关键步骤。