Novel irreversible caspase-1 inhibitor attenuates the maturation of intracellular interleukin-1β

Author:

Ma Xue-Qin12,Zhang Hua-Jie12,Zhang Ya-Hui12,Chen Yi-Hua12,Wu Fang12,Du Jun-Qing12,Yu Hai-Ping12,Zhou Zhong-Liang12,Li Jing-Ya12,Nan Fa-Jun12,Li Jia12

Affiliation:

1. National Center for Drug Screening, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 201203, P.R. China.

2. East China Normal University, Academy of life science, Shanghai 200062, P.R. China.

Abstract

. Caspase-1, the most efficient enzyme in processing the proinflammatory cytokines interleukin 1β and interleukin 18 in humans, is associated with inflammatory diseases such as rheumatoid arthritis, osteoarthritis, and some neuronal diseases. We previously reported that isoquinoline-1,3,4-trione and its derivatives are novel caspase-3 inhibitors that could attenuate apoptosis in vitro and in vivo. Here we report a novel derivative of isoquinoline-1,3,4-trione that is highly potent in inhibiting caspase-1 activity in an irreversible and slow-binding manner, thus inhibiting cellular caspase-1 activity and the maturation of interleukin 1β in U-937 cells.

Publisher

Canadian Science Publishing

Subject

Cell Biology,Molecular Biology,Biochemistry

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