Suppr超能文献

3-(4-甲氧基)-1-(2-(4-香豆素)丙基)-2-烯-1-酮抑制高邮鸭胚胎破骨细胞体外分化。

3-(4-methoxyl)-1-(2-(4-coumarin)prop)-2-en-1-one inhibits the differentiation of Gaoyou duck embryonic osteoclasts in vitro.

机构信息

Department of Biological Sciences, Bengbu Medical College, 2600 Donghai Road, Anhui, Bengbu, CN 233030, China.

State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Guizhou University, Huaxi North Campus, Guiyang, CN 550025, China.

出版信息

Poult Sci. 2019 Apr 1;98(4):1854-1860. doi: 10.3382/ps/pey542.

Abstract

This study determined the influence of 3-(4-methoxyl)-1-(2-(4-coumarin)prop)-2-en-1-one (MCPEO) on the differentiation of Gaoyou duck embryo osteoclasts cultured in vitro. Bone marrow mononuclear cells (BM-MNCs) were harvested from 23-day-old Gaoyou duck embryos and induced by receptor activator of nuclear factor κB ligand (RANKL) and macrophage colony-stimulating factor (M-CSF) in the presence of MCPEO at different concentrations (i.e., 1, 5, 10, 20, and 40 μM). Cell viability measurement, tartrate-resistant acid phosphatase (TRAP) staining, resorption activity assay, and co-staining with Tetramethylrhodamine (TRITC)-conjugated phalloidin and Hoechst 33,258 were conducted. Results indicated that MCPEO influenced the cell viability of the M-CSF + RANKL-induced BM-MNCs in a concentration-dependent manner, reduced the formation of positive multinucleated cells, and restrained the resorption capability of osteoclasts. Microfilament and nuclear staining indicated that MCPEO restricted the differentiation of BM-MNCs into large multinucleated osteoclasts. In short, MCPEO can inhibit the differentiation of BM-MNCs into mature osteoclasts in duck embryos. Therefore, MCPEO is a promising agent for the treatment of poultry osteoporosis.

摘要

本研究旨在探讨 3-(4-甲氧基)-1-(2-(4-香豆素)丙-2-烯-1-酮(MCPEO)对体外培养高邮鸭胚胎破骨细胞分化的影响。取 23 日龄高邮鸭胚胎骨髓单个核细胞(BM-MNCs),在核因子κB 受体激活剂配体(RANKL)和巨噬细胞集落刺激因子(M-CSF)的诱导下,加入不同浓度(1、5、10、20 和 40 μM)的 MCPEO,观察其对细胞活力、抗酒石酸酸性磷酸酶(TRAP)染色、吸光度值、TRITC-鬼笔环肽和 Hoechst 33258 共染色的影响。结果表明,MCPEO 呈浓度依赖性地影响 M-CSF+RANKL 诱导的 BM-MNCs 细胞活力,减少阳性多核细胞的形成,抑制破骨细胞的吸收能力。微丝和核染色表明,MCPEO 抑制了 BM-MNCs 向大型多核破骨细胞的分化。综上所述,MCPEO 可抑制鸭胚胎 BM-MNCs 向成熟破骨细胞的分化。因此,MCPEO 是一种有前途的治疗家禽骨质疏松症的药物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验