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基因表达谱分析显示 Cyp26b1 是一种激活素调节基因,参与卵巢颗粒细胞增殖。

Gene expression profiling reveals Cyp26b1 to be an activin regulated gene involved in ovarian granulosa cell proliferation.

机构信息

Department of Biological Sciences, DePaul University, 2325 North Clifton Avenue, Chicago, Illinois 60614, USA.

出版信息

Endocrinology. 2011 Jan;152(1):303-12. doi: 10.1210/en.2010-0749. Epub 2010 Nov 17.

Abstract

Activin, a member of the TGF-β superfamily, is an important modulator of FSH synthesis and secretion and is involved in reproductive dysfunctions and cancers. It also regulates ovarian follicle development. To understand the mechanisms and pathways by which activin regulates follicle function, we performed a microarray study and identified 240 activin regulated genes in mouse granulosa cells. The gene most strongly inhibited by activin was Cyp26b1, which encodes a P450 cytochrome enzyme that degrades retinoic acid (RA). Cyp26b1 has been shown to play an important role in male germ cell meiosis, but its expression is largely lost in the ovary around embryonic d 12.5. This study demonstrated that Cyp26b1 mRNA was expressed in granulosa cells of follicles at all postnatal developmental stages. A striking inverse spatial and temporal correlation between Cyp26b1 and activin-βA mRNA expression was observed. Cyp26b1 expression was also elevated in a transgenic mouse model that has decreased activin expression. The Cyp26 inhibitor R115866 stimulated the proliferation of primary cultured mouse granulosa cells, and a similar effect was observed with RA and activin. A pan-RA receptor inhibitor, AGN194310, abolished the stimulatory effect of either RA or activin on granulosa cell proliferation, indicating an involvement of RA receptor-mediated signaling. Overall, this study provides new insights into the mechanisms of activin action in the ovary. We conclude that Cyp26b1 is expressed in the postnatal mouse ovary, regulated by activin, and involved in the control of granulosa cell proliferation.

摘要

激活素是 TGF-β 超家族的成员,是 FSH 合成和分泌的重要调节剂,参与生殖功能障碍和癌症。它还调节卵巢卵泡发育。为了了解激活素调节卵泡功能的机制和途径,我们进行了微阵列研究,在小鼠颗粒细胞中鉴定出 240 个激活素调节基因。受激活素抑制最强的基因是 Cyp26b1,它编码一种 P450 细胞色素酶,可降解视黄酸 (RA)。Cyp26b1 在雄性生殖细胞减数分裂中发挥重要作用,但在胚胎第 12.5 天左右卵巢中其表达大量丢失。本研究表明 Cyp26b1mRNA 在出生后所有发育阶段的卵泡颗粒细胞中表达。Cyp26b1 和 activin-βA mRNA 表达之间观察到明显的空间和时间反向相关性。在 activin 表达降低的转基因小鼠模型中,Cyp26b1 的表达也升高。Cyp26 抑制剂 R115866 刺激原代培养的小鼠颗粒细胞增殖,并且在 RA 和激活素中观察到类似的作用。泛 RA 受体抑制剂 AGN194310 消除了 RA 或激活素对颗粒细胞增殖的刺激作用,表明 RA 受体介导的信号转导参与其中。总体而言,这项研究提供了关于激活素在卵巢中作用机制的新见解。我们得出结论,Cyp26b1 在出生后小鼠卵巢中表达,受激活素调节,并参与控制颗粒细胞增殖。

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本文引用的文献

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