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豚鼠精囊分离上皮中的特异性蛋白质合成。去势及雄激素替代的影响。

Specific protein synthesis in isolated epithelium of guinea-pig seminal vesicle. Effects of castration and androgen replacement.

作者信息

Veneziale C M, Burns J M, Lewis J C, Büchi K A

出版信息

Biochem J. 1977 Aug 15;166(2):167-73. doi: 10.1042/bj1660167.

Abstract

Four intrinsic soluble secretory proteins are synthesized in vitro by isolated seminal-vesicle mucosa from sexually mature guinea pigs. Newly synthesized specific proteins labelled with [(14)C]glycine and [(14)C]lysine were precipitated by using double-antibody immunoprecipitation techniques and their radioactivity was assessed. Rates of synthesis were determined on each of 5 days after castration. By 5 days after castration the wet weight of the epithelium decreased to 42% of intact control values; the absolute amount of specific protein synthesized in vitro after 60min incubation decreased to 28% and the 27500g cytoplasmic protein content decreased to 31%. Thus androgen deprivation leads to a decrease in general protein synthesis in vivo, as well as to a decrease in specific protein synthesis in vitro. Specific protein synthesis comprised 76% of the total protein formed in isolated tissue from animals 5 days after castration as compared with 99-100% in tissue from intact animals. At 72h after an injection of testosterone or dihydrotestosterone, seminal-vesicle epithelium wet weight, cytoplasmic protein content and capability for synthesizing specific proteins in vitro were restored to approx. 70% of normal values. At 72h after onset of therapy with 3alpha-androstanediol, both epithelium wet weight and cytoplasmic protein content had increased significantly, but without a corresponding increase in the capability of the isolated tissue to synthesize specific proteins. The soluble labelled proteins synthesized in vitro by isolated epithelium from intact animals during 60 or 120min incubation were essentially entirely immunoprecipitable, i.e. specific. In contrast, approx. 29% of all soluble protein newly synthesized by isolated epithelium from animals 5 days after castration was acid-precipitable, but not immunoprecipitable, i.e. ;non-specific'. The injection of testosterone into castrated animals inhibited the synthesis of the non-specific fraction by isolated tissue. The effects of castration on the ultrastructure of guinea-pig seminal-vesicle epithelium are also presented.

摘要

从性成熟豚鼠分离出的精囊黏膜在体外合成了四种内在可溶性分泌蛋白。利用双抗体免疫沉淀技术沉淀用[(14)C]甘氨酸和[(14)C]赖氨酸标记的新合成的特异性蛋白,并评估其放射性。在去势后的5天内每天测定合成速率。去势后5天,上皮组织的湿重降至完整对照值的42%;孵育60分钟后体外合成的特异性蛋白的绝对量降至28%,27500g细胞质蛋白含量降至31%。因此,雄激素剥夺导致体内总蛋白合成减少,以及体外特异性蛋白合成减少。与完整动物组织中的99 - 100%相比,去势5天后动物分离组织中形成的总蛋白中特异性蛋白合成占76%。注射睾酮或二氢睾酮72小时后,精囊上皮湿重、细胞质蛋白含量和体外合成特异性蛋白的能力恢复到正常水平的约70%。用3α - 雄甾二醇治疗开始72小时后,上皮湿重和细胞质蛋白含量均显著增加,但分离组织合成特异性蛋白的能力没有相应增加。完整动物分离上皮在60或120分钟孵育期间体外合成的可溶性标记蛋白基本上完全可被免疫沉淀,即具有特异性。相比之下,去势5天后动物分离上皮新合成的所有可溶性蛋白中约29%可被酸沉淀,但不能被免疫沉淀,即“非特异性”。给去势动物注射睾酮可抑制分离组织中非特异性部分的合成。还呈现了去势对豚鼠精囊上皮超微结构的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea64/1164991/35aad90f92cf/biochemj00503-0037-a.jpg

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