Ageing Bone Research Program, Sydney Medical School Nepean, The University of Sydney, Penrith, NSW, Australia.
Stem Cells. 2012 May;30(5):1042-8. doi: 10.1002/stem.1063.
Interferon gamma (IFNγ) has been reported to induce osteoblastogenesis from mesenchymal stem cells (MSCs) both in vitro and in vivo. With ageing, adipocytes outnumber osteoblasts within the bone microenvironment leading to a decrease in bone formation. Since both osteoblasts and adipocytes are of mesenchymal origin, we hypothesized that IFNγ treatment might negatively affect adipogenesis while stimulating osteoblastogenesis in human MSC. To test this hypothesis, human MSCs were induced to differentiate into adipocytes in the presence or absence of osteogenic doses of IFNγ (1, 10, and 100 ng/ml). IFNγ-treated MSC showed a decrease in adipocyte differentiation and lipid deposition when compared with vehicle-treated controls. Additionally, adipogenic markers were significantly decreased by IFNγ treatment at the same doses that have been reported to have a strong osteogenic effect in vitro. Furthermore, DNA binding of peroxisome proliferator-activated receptor gamma was significantly lower in IFNγ-treated differentiating MSC. Subsequently, ovariectomized C57BL6 mice were treated with osteogenic doses of IFNγ three times a week for 6 weeks. In distal femur, treated mice showed significantly higher hematopoiesis concomitant with lower levels of fat volume/total volume, adipocyte number, and expression of adipogenic markers when compared with the vehicle-treated mice. Together, these findings demonstrate that, at osteogenic doses, IFNγ also acts as an inhibitor of adipogenesis in vitro and prevents marrow fat infiltration while favors hematopoiesis in ovariectomized mice.
干扰素 γ(IFNγ)已被报道在体外和体内均能诱导间充质干细胞(MSCs)向成骨细胞分化。随着年龄的增长,骨微环境中的脂肪细胞数量超过成骨细胞,导致骨形成减少。由于成骨细胞和脂肪细胞均来源于间充质,我们假设 IFNγ 治疗可能会抑制脂肪生成,同时刺激人 MSC 中的成骨细胞分化。为了验证这一假设,我们在存在或不存在成骨剂量 IFNγ(1、10 和 100ng/ml)的情况下诱导人 MSC 分化为脂肪细胞。与对照组相比,IFNγ 处理的 MSC 显示出脂肪细胞分化和脂质沉积减少。此外,在相同剂量下,IFNγ 处理还显著降低了脂肪生成标记物的表达,而这些剂量已被报道在体外具有很强的成骨作用。此外,IFNγ 处理的分化 MSC 中过氧化物酶体增殖物激活受体 γ 的 DNA 结合明显降低。随后,用成骨剂量 IFNγ 每周三次处理去卵巢 C57BL6 小鼠 6 周。在股骨远端,与对照组相比,治疗组小鼠的造血作用明显增强,同时脂肪体积/总体积、脂肪细胞数量和脂肪生成标记物的表达水平降低。综上所述,这些发现表明,在成骨剂量下,IFNγ 还能体外抑制脂肪生成,并防止骨髓脂肪浸润,同时促进去卵巢小鼠的造血作用。