AN INHIBITOR OF PROSTAGLANDIN BIOSYNTHESIS FROM HUMAN DECIDUA - PARTIAL-PURIFICATION AND PROPERTIES

被引:11
作者
ISHIHARA, O
KINOSHITA, K
SATOH, K
MIZUNO, M
SHIMIZU, T
机构
[1] SAITAMA MED SCH,SAITAMA MED CTR,DEPT OBSTET & GYNAECOL,KAWAGOE,SAITAMA 350,JAPAN
[2] UNIV TOKYO,FAC MED,DEPT PHYSIOL CHEM & NUTR,TOKYO 113,JAPAN
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 1990年 / 40卷 / 03期
关键词
D O I
10.1016/0952-3278(90)90102-Q
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
An inhibitor of prostaglandin synthetase which catalyzes the conversion of arachidonic acid into prostaglandin E2 was partially purified from the 105 00 × g supernatant fraction of the human decidual cell homogenate. By means of ammonium sulfate fractionation, Mono Q ion-exchange chromatography, and gel filtration chromatography, the inhibitor was purified about 15-fold, giving a preparation with a molecular weight of 55-60 KDa. The 50% inhibitory concentration of the purified substance was approximately 0.2 mg/ml. The inhibitor may play a role in suppression of prostaglandin production by decidua in early pregnancy. © 1990.
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页码:223 / 226
页数:4
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