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Computer-aided discovery of novel aryl hydrocarbon receptor ligands to regulate CYP1A1 expression in inflammatory macrophages
被引:0
|作者:
Chen, Kerui
[1
]
Luo, Li
[2
]
Tu, Gao
[3
]
Yang, Jingyi
[3
]
Pu, Wang
[1
]
Zhu, Junyu
[2
]
Xue, Weiwei
[3
]
Zhang, Rui
[1
]
机构:
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Resp & Crit Care Med, 1 Youyi Rd, Chongqing 400016, Peoples R China
[2] Army Med Univ, Army Med Ctr, Res Dept 1, Chongqing, Peoples R China
[3] Chongqing Univ, Sch Pharmaceut Sci, Chongqing 401331, Peoples R China
关键词:
anti-inflammation;
aryl hydrocarbon receptor;
CYP1A1;
ensemble docking;
ligand;
POLYCYCLIC AROMATIC-HYDROCARBONS;
PAS-B DOMAIN;
AHR;
BINDING;
INHIBITION;
RISK;
D O I:
10.1111/cbdd.14572
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The environmental factor aryl hydrocarbon receptor (AhR), a key protein connecting the external environmental signals (e.g., environmental endocrine disruptor TCDD) to internal cellular processes, is involved in the activation of peripheral macrophages and inflammatory response in human body. Thus, there is widespread interest in finding compounds to anti-inflammatory response in macrophages by targeting human AhR. Here, ensemble docking based-virtual screening was first used to screen a library (similar to 200,000 compounds) against human AhR ligand binding domain (LBD) and 25 compounds were identified as potential inhibitors. Then, 9 out of the 25 ligands were found to down-regulate the mRNA expression of CYP1A1 (a downstream gene of AhR signaling) in AhR overexpressing macrophages. The most potent compound AE-411/41415610 was selected for further study and found to reduce both mRNA and protein expressions level of CYP1A1 in mouse peritoneal macrophage. Moreover, protein chip signal pathway analysis indicated that AE-411/41415610 play a role in regulating JAK-STAT and AKT-mTOR pathways. In sum, the discovered hits with novel scaffolds provided a starting point for future design of more effective AhR-targeted lead compounds to regulate CYP1A1 expression of inflammatory peritoneal macrophages.
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