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多种哺乳动物垂体和肾上腺中的嗜铬粒蛋白A、嗜铬粒蛋白B和分泌粒蛋白II信使核糖核酸。雌激素对嗜铬粒蛋白A、嗜铬粒蛋白B和分泌粒蛋白II信使核糖核酸水平的调节。

Chromogranin A, chromogranin B and secretogranin II mRNAs in the pituitary and adrenal glands of various mammals. Regulation of chromogranin A, chromogranin B and secretogranin II mRNA levels by estrogen.

作者信息

Lloyd R V, Hawkins K, Jin L, Kulig E, Fields K

机构信息

Department of Pathology, University of Michigan, Ann Arbor.

出版信息

Lab Invest. 1992 Sep;67(3):394-404.

PMID:1405495
Abstract

BACKGROUND

The chromogranin/secretogranin (Cg/Sg) acidic proteins are widely distributed in vertebrate species. They are thought to play a role in hormone packaging within secretory granules, in hormone secretion, and serve as prohormones for various proteolytic cleavage products. The genes for most members of the Cg/Sg family have been cloned, so hybridization analysis can be used to analyze the distribution and regulation of Cg/Sg mRNAs in various vertebrate species.

EXPERIMENTAL DESIGN

The method of in situ hybridization was used to localize chromogranin A, chromogranin B, and secretogranin II in adrenal and pituitary tissues from laboratory animals and from humans in order to analyze the distribution of various Cg/Sg mRNAs in these tissues. To gain some insight into the regulation and possible functions of specific Cg/Sg members, female rats were ovariectomized for different periods with and without estrogen replacement and the pituitaries were subsequently analyzed by in situ hybridization and Northern hybridization analyses. Combined ISH and immunohistochemistry were used to localize the specific cell types in normal rat pituitary that expressed the mRNA for chromogranin A, chromogranin B, and secretogranin II.

RESULTS

All three Cg/Sg mRNAs were detected in pituitary and adrenal tissues of rats, mice, dogs, monkeys, and humans. Combined in situ hybridization and immunohistochemistry using rat pituitary revealed that the glycoprotein hormone-secreting cells expressed all three Cg/Sg mRNAs in approximately equal amounts. Ovariectomy followed by estrogen replacement resulted in decreased levels of CgA and SgII mRNAs. In contrast, the level of CgB mRNA, that was not changed by ovariectomy, was increased after estrogen treatment, probably secondary to prolactin cell hyperplasia.

CONCLUSIONS

The three principal Cg/Sg mRNAs are present in the adrenal and pituitary of various vertebrates. Estrogen plays a significant role in regulating the mRNA levels of different Cgs/Sgs suggesting functional and regulatory differences in Cg/Sg proteins.

摘要

背景

嗜铬粒蛋白/分泌粒蛋白(Cg/Sg)酸性蛋白广泛分布于脊椎动物物种中。它们被认为在分泌颗粒内的激素包装、激素分泌中发挥作用,并作为各种蛋白水解裂解产物的前体激素。Cg/Sg家族大多数成员的基因已被克隆,因此杂交分析可用于分析Cg/Sg mRNA在各种脊椎动物物种中的分布和调控。

实验设计

采用原位杂交方法对实验动物和人类的肾上腺及垂体组织中的嗜铬粒蛋白A、嗜铬粒蛋白B和分泌粒蛋白II进行定位,以分析这些组织中各种Cg/Sg mRNA的分布。为了深入了解特定Cg/Sg成员的调控及可能的功能,对雌性大鼠进行不同时期的卵巢切除,有无雌激素替代,随后通过原位杂交和Northern杂交分析垂体。联合原位杂交和免疫组化用于定位正常大鼠垂体中表达嗜铬粒蛋白A、嗜铬粒蛋白B和分泌粒蛋白II mRNA的特定细胞类型。

结果

在大鼠、小鼠、狗、猴子和人类的垂体和肾上腺组织中均检测到所有三种Cg/Sg mRNA。使用大鼠垂体进行的联合原位杂交和免疫组化显示,分泌糖蛋白激素的细胞以大致相等的量表达所有三种Cg/Sg mRNA。卵巢切除后雌激素替代导致CgA和SgII mRNA水平降低。相反,卵巢切除未改变的CgB mRNA水平在雌激素处理后升高,可能继发于催乳素细胞增生。

结论

三种主要的Cg/Sg mRNA存在于各种脊椎动物的肾上腺和垂体中。雌激素在调节不同Cg/Sg的mRNA水平中起重要作用,提示Cg/Sg蛋白在功能和调控上存在差异。

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