首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Effect of Bacillus subtilis spore administration on activation of macrophages and natural killer cells in mice
Authors:T Kosaka  T Maeda  Y Nakada  M Yukawa  S Tanaka
Institution:

a Laboratory of Veterinary Surgery, School of Veterinary Medicine, Nihon University, Kameino 1866, Fujisawa, Kanagawa, 252, Japan

b Laboratory of Veterinary Radiology, School of Veterinary Medicine, Nihon University, Kameino 1866, Fujisawa, Kanagawa, 252, Japan

c Laboratory of Laboratory Animal, School of Veterinary Medicine, Nihon University, Kameino 1866, Fujisawa, Kanagawa, 252, Japan

Abstract:The effect of Bacillus subtilis (strain A102) spores on the activation of murine macrophages and natural killer cells (NK) was examined. The macrophage activity and NK activity were enhanced by oral administration of A102 spores, and slightly enhanced by oral administration of culture supernatant. There was no difference in the results of macrophage activity and NK activity using other live or dead spores. The NK activity and macrophage activity were increased with increments of concentration up to 0.1 g per mouse, and both activities were decreased at concentration of more than 0.15 g per mouse. The NK activity was increased 1 and 2 days after oral administration of A102 spores, and the activity level 2 days after administration was about 3-fold higher than the level prior to treatment. Macrophage activity was also increased from 1 to 3 days after oral administration of A102 spores, and the activity level 3 days after administration was about 3-fold higher than the level prior to treatment. The induction of interferons at 1 day after oral administration in mouse serum was 5-fold higher than that in controls. These findings indicate that oral administration of A102 gave rise to the induction of interferons, and it is likely that macrophages and NK cells were activated by interferons.
Keywords:Bacillus subtilis  Mouse  Interferon  Macrophages  Natural killer cells
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号