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8-硝基-cGMP 是 RANKL 诱导的破骨细胞分化的促进剂。

8-Nitro-cGMP is a promoter of osteoclast differentiation induced by RANKL.

机构信息

Department of Biochemistry, Showa University School of Dentistry, Japan; Department of Oral and Maxillofacial Surgery, Tokyo Medical University, Japan.

Department of Biochemistry, Showa University School of Dentistry, Japan.

出版信息

Nitric Oxide. 2018 Jan 30;72:46-51. doi: 10.1016/j.niox.2017.11.006. Epub 2017 Nov 26.

Abstract

Osteoclasts are multinucleated giant cells differentiated from monocyte-macrophage-lineage cells under stimulation of receptor activator of nuclear factor κ-B (RANK) ligand (RANKL) produced by osteoblasts and osteocytes. Although it has been reported that nitric oxide (NO) and reactive oxygen species (ROS) are involved in this process, the mechanism by which these labile molecules promote osteoclast differentiation are not fully understood. In this study, we investigated the formation and function of 8-nitro-cGMP, a downstream molecule of NO and ROS, in the process of osteoclast differentiation in vitro. 8-Nitro-cGMP was detected in mouse bone marrow macrophages and osteoclasts differentiated from macrophages in the presence of RANKL. Inhibition of NO synthase suppressed the formation of 8-nitro-cGMP as well as RANKL-induced osteoclast differentiation from macrophages. On the other hand, RANKL-induced osteoclast differentiation was promoted by addition of 8-nitro-cGMP to the cultures. In addition, 8-nitro-cGMP enhanced the mRNA expression of RANK, the receptor for RANKL. However, 8-bromo-cGMP, a membrane-permeable derivative of cGMP, did not have an effect on either RANKL-induced osteoclast differentiation or expression of the RANK gene. These results suggest that 8-nitro-cGMP is a novel positive regulator of osteoclast differentiation, which might help to explain the roles of NO and ROS in osteoclast differentiation.

摘要

破骨细胞是由成骨细胞和骨细胞产生的核因子κ-B 受体激活剂(RANK)配体(RANKL)刺激单核细胞-巨噬细胞谱系细胞分化而来的多核巨细胞。虽然已经报道一氧化氮(NO)和活性氧(ROS)参与了这一过程,但这些不稳定分子促进破骨细胞分化的机制尚不完全清楚。在这项研究中,我们研究了 8-硝基-cGMP(NO 和 ROS 的下游分子)在体外破骨细胞分化过程中的形成和功能。在 RANKL 存在的情况下,在小鼠骨髓巨噬细胞和由巨噬细胞分化而来的破骨细胞中检测到 8-硝基-cGMP。NO 合酶的抑制抑制了 8-硝基-cGMP 的形成以及 RANKL 诱导的巨噬细胞向破骨细胞的分化。另一方面,向培养物中添加 8-硝基-cGMP 可促进 RANKL 诱导的破骨细胞分化。此外,8-硝基-cGMP 增强了 RANKL 诱导的破骨细胞分化中 RANK(RANKL 的受体)的 mRNA 表达。然而,cGMP 的膜通透衍生物 8-溴-cGMP 对 RANKL 诱导的破骨细胞分化或 RANK 基因的表达均没有影响。这些结果表明,8-硝基-cGMP 是破骨细胞分化的新型正调节剂,这可能有助于解释 NO 和 ROS 在破骨细胞分化中的作用。

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