Effects of Benzoxazole Derivative PO- 296 on Dendritic Cell Differentiation and Related Indexes
- VernacularTitle:苯并噁唑衍生物PO-296对树突状细胞分化及相关指标的影响
- Author:
Xinying ZHU
1
;
Miao YANG
2
;
Can XU
2
;
Xu PENG
1
;
Jiayi DUAN
1
;
Dan LIU
1
;
Yantang WANG
1
Author Information
1. School of Pharmacy，Chengdu Medical College，Chengdu 610083，China
2. School of Clinical Medicine，Chengdu Medical College，Chengdu 610083，China
- Publication Type:Journal Article
- Keywords:
PO-296;
Dendritic cell;
Specific surface molecules;
Inflammatory cytokines;
Phagocytic function;
Cytotoxicity
- From:
China Pharmacy
2019;30(18):2474-2480
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE： To investigate the effects of benzoxazole derivative 2-（chlorobenzoxazolyl-2-yl）-4，5，6，7-tetrahydro- dihydro-indazole-3-ol （PO-296） on the differentiation of murine bone marrow-derived dendritic cells（DC） and their related indexes as specific surface molecules and inflammatory cytokines. METHODS： Bone marrow nuclear cells of mice were isolated， and immature DC （imDC） was obtained by recombinant mice granulocyte macrophage colony-stimulating factor and recombinant mice IL-4. After pretreated with low-dose， medium-dose and high-dose （1， 5， 25 μmol/L） of PO-296， DC was obtained by lipopolysaccharide induction. Flow cytometry was used to detect the expression of DC specific surface molecules [i.e. the proportion of class Ⅱ major histocompatibility complex （MHC Ⅱ）， CD80， CD86 and chemokine receptor 7 （CCR7） positive cells]， imDC phagocytosis （i.e. the proportion of dextran positive cells） and DC survival （i.e. the proportion of survival cells）. ELISA method was used to detect the levels of inflammatory cytokines （IL-10， IL-12 and TNF-α） in cell culture medium. RESULTS： Compared with imDC group， the proportion of MHC Ⅱ， CD80 and CD86 positive cells were increased significantly in non-loading group （P＜0.05）. Compared with non-loading group， the levels of IL-10 in cell culture medium were increased significantly in PO-296 groups. The proportions of MHC Ⅱ， CD80 and CD86 positive cells in positive group and PO-296 medium-dose and high-dose groups as well as the levels of IL-12 and TNF-α in cell culture medium in administration groups were decreased significantly （P＜0.05）. There was no statistical significance in the proportion of CCR7 positive cells， dextran positive cells and survival cells in administration groups， compared with non-loading group （P＞0.05）. CONCLUSIONS： PO-296 has no obvious cytotoxicity and does not affect the phagocytic function of imDC. At the same time， the compound can inhibit the expression of DC specific surface molecules and regulate the secretion of inflammatory cytokines.
