期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
Arbuscular mycorrhizal for-mation of crucifer leaf mus-tard induced by flavonoids apigenin and daidzein 被引量:2
1
作者 DONG Changjin1,2 & ZHAO Bin1 1. State Key Laboratory of Agricultural Microbiology, Huazhong Agri- cultural University, Wuhan 430070, China 2. Department of Biology, Hubei Normal University, Huangshi 435002, China 《Chinese Science Bulletin》 SCIE EI CAS 2004年第12期1254-1261,共8页
Flavonoids from legume root secretion may probably act as signal molecules for expression of Rhizobial “nod” nodulation genes and AM fungal symbiotic gene. Leaf mustard is a non-mycorrhizal plant; it does not contai... Flavonoids from legume root secretion may probably act as signal molecules for expression of Rhizobial “nod” nodulation genes and AM fungal symbiotic gene. Leaf mustard is a non-mycorrhizal plant; it does not contain fla- vonoids and other signal molecules. AM fungi could not in- fect the roots of leaf mustard and form a symbiont in nature, when it was treated with flavonoids (apigenin or daidzein). The results of trypan blue staining showed that two kinds of AM fungi (G. intraradices and G. mosseae) successfully in- fected the roots of non-mycorrhizal plant leaf mustard. AM fungi grew towards and colonized the roots of leaf mustard, producing young spores and completing the course of life. AM fungi are the only one kind of fungi with ALP activity. The result of ALP staining has also proved that AM fungi infected successfully the roots of leaf mustard. AM fungi (G. intraradices and G. mosseae) that existed in the roots of non-mycorrhizal plant leaf mustard were probed by nested PCR and special molecular probes. The above-mentioned proof chains have fully proved that flavonoids induced AM fungi (G. intraradices and G. mosseae) to infect non-my- corrhizal plant and establish symbiotic relationship. 展开更多
关键词 非菌根植物 免疫 十字花科叶芥菜 甙元 大豆黄酮 类黄酮 灌木菌根真菌 嵌套PCR trypan蓝色染色
原文传递
芹甙元抑制破骨细胞分化的机制研究 被引量:1
2
作者 穆培 丁欢 +1 位作者 许志兴 陆雄伟 《医学研究杂志》 2021年第10期115-119,共5页
目的探讨芹甙元抑制破骨细胞分化机制。方法小鼠骨髓巨噬细胞(BMMs)分不同浓度的芹甙元组,通过CCK-8法检测芹甙元对BMMs的细胞毒性,抗酒石酸酶(TRAP)染色法检测各组成熟破骨细胞数量,荧光定量聚合酶法(qPCR)检测各组破骨细胞分化标志基... 目的探讨芹甙元抑制破骨细胞分化机制。方法小鼠骨髓巨噬细胞(BMMs)分不同浓度的芹甙元组,通过CCK-8法检测芹甙元对BMMs的细胞毒性,抗酒石酸酶(TRAP)染色法检测各组成熟破骨细胞数量,荧光定量聚合酶法(qPCR)检测各组破骨细胞分化标志基因(NFATC1、TRAP、CTSK、Atp6v0d2、Dc-stamp、C-Fos)mRNA的表达,Western blot法检测核转录因子κB p65(NF-κB p65)中磷酸化蛋白的水平。结果CCK-8检测结果显示,芹甙元在50μmol/L范围内对BMMs无明显的细胞毒性;TRAP染色结果显示,TRAP染色阳性的破骨细胞数目随着芹甙元浓度的升高而减少;qPCR检测结果显示,随着芹甙元浓度的升高,破骨细胞分化基因(NFATC1、TRAP、CTSK、Atp6v0d2、Dc-stamp、C-Fos mRNA)mRNA的表达水平明显降低(P<0.05);Western blot法检测结果显示,芹甙元组p65的磷酸化水平相对于对照组明显降低(P<0.05)。结论芹甙元可以通过NF-κB通路抑制破骨细胞分化与成熟,有望作为治疗骨质疏松骨溶解的潜在药物。 展开更多
关键词 甙元 破骨细胞 骨质疏松
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部