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小鼠胚胎在响应致畸剂量的视黄酸时,提高细胞视黄醇结合蛋白mRNA水平的能力有限。

Mouse conceptuses have a limited capacity to elevate the mRNA level of cellular retinoid binding proteins in response to teratogenic doses of retinoic acid.

作者信息

Harnish D C, Soprano K J, Soprano D R

机构信息

Department of Biochemistry, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.

出版信息

Teratology. 1992 Aug;46(2):137-46. doi: 10.1002/tera.1420460207.

Abstract

In these studies, we wished to determine the effect of teratogenic doses of retinoic acid on the expression of cellular retinoic acid binding protein I (CRABP-I) mRNA, cellular retinoic acid binding protein II (CRABP-II) mRNA, cellular retinol binding protein I (CRBP-I) mRNA, and cellular retinol binding protein II (CRBP-II) mRNA in mouse conceptuses. Levels of CRABP-II mRNA and CRBP-I mRNA were modestly elevated (2.5-fold and 1.5-fold, respectively) in 9-day gestation conceptuses following treatment of dams with 100 mg/kg b.w. of retinoic acid. These levels were elevated by 6 hr following treatment and remained elevated until 48 and 24 hr, respectively. Two other retinoids, etretinate and retinoyl beta-glucuronide, also moderately elevated CRABP-II mRNA and CRBP-I mRNA levels in conceptuses. In contrast, the levels of CRABP-I mRNA in the conceptuses remained unaffected by treatment with any of these three retinoids. These results demonstrate that conceptuses have a limited capacity to elevate the cellular retinoid binding proteins mRNA levels and presumably the synthesis of their respective proteins in response to high, teratogenic doses of retinoic acid. As a result, an excess of free retinoic acid becomes available to the nuclear retinoic acid receptors, which may lead to inappropriate gene expression and eventual maldevelopment.

摘要

在这些研究中,我们希望确定致畸剂量的视黄酸对小鼠胚胎中细胞视黄酸结合蛋白I(CRABP-I)mRNA、细胞视黄酸结合蛋白II(CRABP-II)mRNA、细胞视黄醇结合蛋白I(CRBP-I)mRNA和细胞视黄醇结合蛋白II(CRBP-II)mRNA表达的影响。在用100mg/kg体重的视黄酸处理母鼠后,妊娠9天的胚胎中CRABP-II mRNA和CRBP-I mRNA水平适度升高(分别为2.5倍和1.5倍)。处理后6小时这些水平升高,并分别持续升高至48小时和24小时。另外两种类视黄醇,依曲替酯和视黄酰β-葡萄糖醛酸,也使胚胎中的CRABP-II mRNA和CRBP-I mRNA水平适度升高。相比之下,这三种类视黄醇中的任何一种处理都不会影响胚胎中CRABP-I mRNA的水平。这些结果表明,胚胎响应高剂量致畸视黄酸而升高细胞类视黄醇结合蛋白mRNA水平以及推测其各自蛋白质合成的能力有限。结果,过量的游离视黄酸可被核视黄酸受体利用,这可能导致不适当的基因表达和最终的发育异常。

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