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细胞视黄酸结合蛋白II在大鼠卵巢中的诱导表达:黄体发育过程中的促性腺激素调节。

Inducible expression of cellular retinoic acid-binding protein II in rat ovary: gonadotropin regulation during luteal development.

作者信息

Bucco R A, Melner M H, Gordon D S, Leers-Sucheta S, Ong D E

机构信息

Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.

出版信息

Endocrinology. 1995 Jun;136(6):2730-40. doi: 10.1210/endo.136.6.7750498.

Abstract

Two members of the superfamily of small intracellular carrier proteins for lipophilic compounds are cellular retinoic acid-binding protein and cellular retinoic acid-binding protein II [CRABP(II)]. CRABP is found in many adult tissues, whereas CRABP(II) is more restricted and is reported as abundant primarily in skin. Here we report a much greater expression of CRABP(II) in rat corpus luteum than in any other organ/tissue examined, including skin. A rat complementary DNA clone encoding CRABP(II) was isolated and the ovarian expression followed during gonadotropin induction of follicular development in the pseudopregnant rat. The pattern of rat CRABP(II) messenger RNA and protein expression correlated with the appearance of corpora lutea and the rise in progesterone production as the corpora lutea developed, and was similar to the induction of 3 beta-hydroxysteroid dehydrogenase. Immunohistochemical localization revealed that CRABP(II) appeared in luteal cells and was dramatically restricted to their cytoplasmic compartment, with no apparent presence in the nucleus. This suggests that CRABP(II) may be expressed to restrict retinoic acid from occupying nuclear retinoic acid receptors, implying that the differentiation and maintenance of the rat corpus luteum may involve in part a release of certain pathways from retinoid suppression.

摘要

亲脂性化合物的小细胞内载体蛋白超家族的两个成员是细胞视黄酸结合蛋白和细胞视黄酸结合蛋白II [CRABP(II)]。CRABP存在于许多成年组织中,而CRABP(II)分布更局限,据报道主要在皮肤中含量丰富。在此我们报告,与包括皮肤在内的任何其他所检测的器官/组织相比,大鼠黄体中CRABP(II)的表达要高得多。分离出了编码CRABP(II)的大鼠互补DNA克隆,并在假孕大鼠促性腺激素诱导卵泡发育过程中追踪其在卵巢中的表达。随着黄体的发育,大鼠CRABP(II)信使核糖核酸和蛋白质表达模式与黄体的出现以及孕酮产生的增加相关,并且与3β - 羟基类固醇脱氢酶的诱导相似。免疫组织化学定位显示,CRABP(II)出现在黄体细胞中,并且显著局限于其细胞质区室,在细胞核中无明显存在。这表明CRABP(II)的表达可能是为了限制视黄酸占据核视黄酸受体,这意味着大鼠黄体的分化和维持可能部分涉及从类维生素A抑制中释放某些途径。

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