Inagawa Hiroyuki, Kobayashi Yutaro, Kohchi Chie, Zhang Ran, Shibasaki Yasuhiro, Soma Gen-Ichiro
Department of Integrated and Holistic Immunology, Faculty of Medicine, Kagawa University, Kagawa, Japan Control of Innate Immunity, Technology Research Association, Kagawa, Japan
Department of Integrated and Holistic Immunology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
In Vivo. 2016 May-Jun;30(3):205-11.
BACKGROUND/AIM: Bacterial lipopolysaccharide (LPS) is involved in the activation of the innate immune responses on monocytes/macrophages in vitro, and by intravenous injection. Although small quantities of LPS are usually found in traditional Chinese medicines, vegetables and fruits, the mode of action of orally administered LPS is still unclear.
LPS derived from Pantoea agglomerans (LPSp) was orally administered to C3H/HeN or C3H/HeJ mice ad libitum.
The LPSp treatment enhanced phagocytosis by resident peritoneal macrophages of C3H/HeN mice but not of C3H/HeJ mice. This activation can be defined as primed activation because no augmentation of inflammatory cytokines production was detected. LPSp in peritoneal fluid was detected and successfully quantified. Moreover, the LPSp reduced the expression of avian reticuloendotheliosis viral oncogene-related B (RelB) in the macrophages without degradation of nuclear factor of kappa light polypeptide gene enhancer in B-cell inhibitor, alpha (IκBα).
Orally administered LPSp can reach the peritoneum, and enhance phagocytosis via Toll-like receptor 4 signaling pathway in resident peritoneal macrophages.
背景/目的:细菌脂多糖(LPS)在体外以及通过静脉注射参与单核细胞/巨噬细胞固有免疫反应的激活。尽管在传统中药、蔬菜和水果中通常会发现少量LPS,但口服LPS的作用方式仍不清楚。
将来源于成团泛菌的LPS(LPSp)随意口服给予C3H/HeN或C3H/HeJ小鼠。
LPSp处理增强了C3H/HeN小鼠而非C3H/HeJ小鼠的驻留腹膜巨噬细胞的吞噬作用。这种激活可被定义为预激活,因为未检测到炎性细胞因子产生的增加。检测并成功定量了腹膜液中的LPSp。此外,LPSp降低了巨噬细胞中禽网状内皮组织增生症病毒癌基因相关B(RelB)的表达,而未降解B细胞抑制剂α(IκBα)中的κ轻链多肽基因增强子的核因子。
口服LPSp可到达腹膜,并通过Toll样受体4信号通路增强驻留腹膜巨噬细胞的吞噬作用。