Vaira Sergio, Alhawagri Muhammad, Anwisye Imani, Kitaura Hideki, Faccio Roberta, Novack Deborah Veis
Division of Bone and Mineral Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
J Clin Invest. 2008 Jun;118(6):2088-97. doi: 10.1172/JCI33392.
Osteoclasts (OCs) function to reabsorb bone and are responsible for the bone loss associated with inflammatory arthritis and osteoporosis. OC numbers are elevated in most disorders of accelerated bone destruction, reflecting altered rates of precursor differentiation and apoptosis. Both of these processes are regulated by the JNK family of MAP kinases. In this study, we have demonstrated that the NF-kappaB subunit RelA/p65 inhibits JNK-mediated apoptosis during a critical period of commitment to the OC phenotype in response to the cytokine RANKL. This RelA/p65-mediated arrest of cell death led to enhanced OC differentiation. Hence, Rela-/- OC precursors displayed prolonged JNK activation in response to RANKL, and this was accompanied by an increase in cell death that prevented efficient differentiation. Although complete blockade of JNK activity inhibits osteoclastogenesis, both short-term blockade in RelA-deficient cultures and suppression of the downstream mediator, Bid rescued apoptosis and differentiation. These antiapoptotic effects were RelA specific, as overexpression of RelA, but not RelB, blocked apoptosis and rescued differentiation in Rela-/- precursors. Thus, RelA blocks a RANKL-induced, apoptotic JNK-Bid pathway, thereby promoting OC differentiation. Consistent with this, mice lacking RelA/p65 in the hematopoietic compartment were shown to have a deficient osteoclastogenic response to RANKL and were protected from arthritis-induced osteolysis.
破骨细胞(OCs)的功能是重吸收骨骼,并导致与炎性关节炎和骨质疏松症相关的骨质流失。在大多数加速骨质破坏的疾病中,破骨细胞数量会增加,这反映了前体细胞分化和凋亡速率的改变。这两个过程均受丝裂原活化蛋白激酶(MAP激酶)的JNK家族调控。在本研究中,我们已经证明,核因子κB亚基RelA/p65在响应细胞因子RANKL而向破骨细胞表型分化的关键时期,抑制JNK介导的凋亡。这种RelA/p65介导的细胞死亡停滞导致破骨细胞分化增强。因此,RelA基因敲除的破骨细胞前体细胞在响应RANKL时显示出JNK的持续激活,同时伴随着细胞死亡增加,从而阻止了有效的分化。虽然完全阻断JNK活性会抑制破骨细胞生成,但在RelA缺陷型培养物中短期阻断以及抑制下游介质Bid均可挽救凋亡和分化。这些抗凋亡作用具有RelA特异性,因为RelA(而非RelB)的过表达可阻断RelA基因敲除前体细胞中的凋亡并挽救分化。因此,RelA阻断RANKL诱导的凋亡性JNK-Bid途径,从而促进破骨细胞分化。与此一致的是,造血系统中缺乏RelA/p65的小鼠对RANKL的破骨细胞生成反应不足,并免受关节炎诱导的骨质溶解。