15-deoxy-Δ12,14-prostalandin J2, a ligand for peroxisome proliferator-activated receptor-γ, induces apoptosis in JEG3 choriocarcinoma cells

被引:110
作者
Keelan, JA [1 ]
Sato, TA [1 ]
Marvin, KW [1 ]
Lander, J [1 ]
Gilmour, RS [1 ]
Mitchell, MD [1 ]
机构
[1] Univ Auckland, Sch Med, Fac Med & Hlth Sci, Dept Pharmacol & Clin Pharmacol, Auckland, New Zealand
关键词
D O I
10.1006/bbrc.1999.1257
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
Apoptosis has been described in placental (trophoblast) tissues during both normal and abnormal pregnancies. We have studied the effects of the cyclopentenone prostaglandins (PGs) on trophoblast cell death using JEG3 choriocarcinoma cells. PGJ(2), Delta(12)PGJ(2), and 15-deoxy-Delta(12,14)-PGJ(2) (15dPGJ(2)) (10 mu M) significantly reduced mitochondrial activity (MTT assay) over 16 h by 17.4 +/- 4.7%, 28 +/- 9.3%, and 62.5 +/- 2.8%, respectively (mean +/- sem), while PGA(2) and PGD(2) had no effect. The synthetic PPAR-gamma ligand ciglitizone (12.5 mu M) had a potency similar to 15dPGJ(2) (69 +/- 3% reduction). Morphological examination of cultures treated with PGJ(2) and its derivatives revealed the presence of numerous cells with dense, pyknotic nuclei, a hallmark of apoptosis. FACS analysis revealed an abundance (similar to 40%) of apoptotic cells after 16-h treatment with 15dPGJ(2) (10 mu M). The caspase inhibitor ZVAD-fmk (5 mu M) significantly diminished the apoptotic effects of Delta(12)PGJ(2) and 15dPGJ(2). JEG3 cells expressed PPAR-gamma mRNA by Northern analysis. These novel findings imply a role for PPAR-gamma ligands in various processes associated with pregnancy and parturition. (C) 1999 Academic Press.
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页码:579 / 585
页数:7
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