Bozec Aline, Bakiri Latifa, Hoebertz Astrid, Eferl Robert, Schilling Arndt F, Komnenovic Vukoslav, Scheuch Harald, Priemel Matthias, Stewart Colin L, Amling Michael, Wagner Erwin F
Research Institute of Molecular Pathology (I.M.P.), Dr. Bohr-Gasse 7, A-1030 Vienna, Austria.
Nature. 2008 Jul 10;454(7201):221-5. doi: 10.1038/nature07019. Epub 2008 Jun 11.
Osteoclasts are multinucleated haematopoietic cells that resorb bone. Increased osteoclast activity causes osteoporosis, a disorder resulting in a low bone mass and a high risk of fractures. Increased osteoclast size and numbers are also a hallmark of other disorders, such as Paget's disease and multiple myeloma. The protein c-Fos, a component of the AP-1 transcription factor complex, is essential for osteoclast differentiation. Here we show that the Fos-related protein Fra-2 controls osteoclast survival and size. The bones of Fra-2-deficient newborn mice have giant osteoclasts, and signalling through leukaemia inhibitory factor (LIF) and its receptor is impaired. Similarly, newborn animals lacking LIF have giant osteoclasts, and we show that LIF is a direct transcriptional target of Fra-2 and c-Jun. Moreover, bones deficient in Fra-2 and LIF are hypoxic and express increased levels of hypoxia-induced factor 1alpha (HIF1alpha) and Bcl-2. Overexpression of Bcl-2 is sufficient to induce giant osteoclasts in vivo, whereas Fra-2 and LIF affect HIF1alpha through transcriptional modulation of the HIF prolyl hydroxylase PHD2. This pathway is operative in the placenta, because specific inactivation of Fra-2 in the embryo alone does not cause hypoxia or the giant osteoclast phenotype. Thus placenta-induced hypoxia during embryogenesis leads to the formation of giant osteoclasts in young pups. These findings offer potential targets for the treatment of syndromes associated with increased osteoclastogenesis.
破骨细胞是负责骨吸收的多核造血细胞。破骨细胞活性增加会导致骨质疏松症,这种病症会导致骨量降低以及骨折风险升高。破骨细胞大小和数量增加也是其他病症的一个标志,比如佩吉特氏病和多发性骨髓瘤。蛋白c-Fos是AP-1转录因子复合体的一个组成部分,对破骨细胞分化至关重要。我们在此表明,Fos相关蛋白Fra-2控制破骨细胞的存活和大小。Fra-2基因缺陷型新生小鼠的骨骼中有巨大破骨细胞,并且通过白血病抑制因子(LIF)及其受体的信号传导受损。同样,缺乏LIF的新生动物也有巨大破骨细胞,并且我们表明LIF是Fra-2和c-Jun的直接转录靶标。此外,缺乏Fra-2和LIF的骨骼处于低氧状态,并且缺氧诱导因子1α(HIF1α)和Bcl-2的表达水平升高。Bcl-2的过表达足以在体内诱导产生巨大破骨细胞,而Fra-2和LIF通过对HIF脯氨酰羟化酶PHD2的转录调节来影响HIF1α。这条通路在胎盘中起作用,因为仅在胚胎中特异性失活Fra-2不会导致缺氧或巨大破骨细胞表型。因此,胚胎发育过程中胎盘诱导的缺氧会导致幼崽体内形成巨大破骨细胞。这些发现为治疗与破骨细胞生成增加相关的综合征提供了潜在靶点。