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过氧化物酶体增殖物激活受体γ以配体特异性方式调节人滋养层细胞的分化。

Peroxisome proliferator-activated receptor-gamma modulates differentiation of human trophoblast in a ligand-specific manner.

作者信息

Schaiff W T, Carlson M G, Smith S D, Levy R, Nelson D M, Sadovsky Y

机构信息

Department of Obstetrics and Gynecology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

J Clin Endocrinol Metab. 2000 Oct;85(10):3874-81. doi: 10.1210/jcem.85.10.6885.

Abstract

The ligand-dependent nuclear receptor peroxisome proliferator-activated receptor-gamma (PPARgamma) regulates the differentiation of several tissues and cell types. PPARgamma was recently determined to be essential for murine placental development and differentiation. We therefore assessed the influence of PPARgamma on differentiation of human placental trophoblasts. We initially used immunohistochemistry to examine term human placentas for PPARgamma expression and found that PPARgamma is present in syncytiotrophoblasts and cytotrophoblasts in placental villi. We correlated the expression of PPARgamma with differentiation of primary human trophoblasts and found that 8-bromo-cAMP, a known enhancer of trophoblast differentiation, stimulates PPARgamma activity, but has no effect on PPARgamma expression. We demonstrated that the PPARgamma ligand 15-deoxy-delta12,14-prostaglandin J2 (15deltaPGJ2) and the thiazolidinedione troglitazone stimulate PPARgamma activity in the trophoblast cell line BeWo. Importantly, whereas exposure of cultured primary trophoblasts to troglitazone enhances biochemical and morphological trophoblast differentiation, 15deltaPGJ2 diminishes trophoblast differentiation. Furthermore, 15deltaPGJ2, but not troglitazone, up-regulates p53 expression and promotes trophoblast apoptosis. These data indicate that PPARgamma is expressed in human placental trophoblasts, and that ligand-specific activation of PPARgamma results in opposing effects on trophoblast differentiation. Our results suggest that PPARgamma plays an important role in placental differentiation during human pregnancy.

摘要

配体依赖性核受体过氧化物酶体增殖物激活受体γ(PPARγ)调节多种组织和细胞类型的分化。最近确定PPARγ对小鼠胎盘发育和分化至关重要。因此,我们评估了PPARγ对人胎盘滋养层细胞分化的影响。我们最初使用免疫组织化学检查足月人胎盘的PPARγ表达,发现PPARγ存在于胎盘绒毛的合体滋养层细胞和细胞滋养层细胞中。我们将PPARγ的表达与原代人滋养层细胞的分化相关联,发现8-溴环磷腺苷(8-bromo-cAMP)是一种已知的滋养层细胞分化增强剂,可刺激PPARγ活性,但对PPARγ表达没有影响。我们证明PPARγ配体15-脱氧-Δ12,14-前列腺素J2(15d-PGJ2)和噻唑烷二酮类药物曲格列酮可刺激滋养层细胞系BeWo中的PPARγ活性。重要的是,虽然将培养的原代滋养层细胞暴露于曲格列酮可增强滋养层细胞的生化和形态学分化,但15d-PGJ2会减弱滋养层细胞分化。此外,15d-PGJ2而非曲格列酮上调p53表达并促进滋养层细胞凋亡。这些数据表明PPARγ在人胎盘滋养层细胞中表达,并且PPARγ的配体特异性激活对滋养层细胞分化产生相反的影响。我们的结果表明PPARγ在人类妊娠期间的胎盘分化中起重要作用。

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