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大鼠精囊分泌泡中不同区室的免疫电子显微镜证据。

Immunoelectron microscopic evidence for different compartments in the secretory vacuoles of the rat seminal vesicles.

作者信息

Aumüller G, Seitz J

出版信息

Histochem J. 1986 Jan;18(1):15-23. doi: 10.1007/BF01676193.

DOI:10.1007/BF01676193
PMID:2423477
Abstract

Immunoelectron microscopy of the rat seminal vesicle was performed using specific antibodies to secretory proteins. Proteins were precipitated from rat seminal vesicle secretion and were separated by SDS-polyacrylamide gel electrophoresis. Among the great number of bands the two most prominent bands were selected and designated SVS II and IV. Their apparent molecular weights were 48 kDa and 16.5 kDa respectively. The bands were excised from the gels and used for antibody production in rabbits. The respective antisera were used for immunohistochemical studies both at the light and electron microscopic levels in the rat seminal vesicle and the different prostatic lobes in infantile, adult and castrated animals. A positive immunoreaction was observed in seminal vesicle and lateral prostatic epithelium of the intact adult rat, while it was lacking in prepubertal and castrated animals. The subcellular distribution of both proteins was clearly different: SVS II was exclusively confined to the electron dense core of the secretory vacuoles, while SVS IV was detected only in the clear halo surrounding the central granule. It is suggested that the spatial arrangement of both proteins in the seminal vesicle secretion vacuole reflects a particular functional significance of each of these proteins. These proteins may serve as a tool in the study of regulation of androgen-dependent protein synthesis.

摘要

利用针对分泌蛋白的特异性抗体对大鼠精囊进行免疫电子显微镜检查。从大鼠精囊分泌物中沉淀蛋白质,并通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳进行分离。在众多条带中,选择了两条最明显的条带,分别命名为SVS II和IV。它们的表观分子量分别为48 kDa和16.5 kDa。从凝胶中切下这些条带,用于在兔体内制备抗体。各自的抗血清用于在光镜和电镜水平对大鼠精囊以及幼年、成年和去势动物的不同前列腺叶进行免疫组织化学研究。在完整成年大鼠的精囊和前列腺外侧上皮中观察到阳性免疫反应,而在青春期前和去势动物中则没有。两种蛋白质的亚细胞分布明显不同:SVS II仅局限于分泌泡的电子致密核心,而SVS IV仅在围绕中央颗粒的透明晕中检测到。有人认为,这两种蛋白质在精囊分泌泡中的空间排列反映了每种蛋白质的特定功能意义。这些蛋白质可作为研究雄激素依赖性蛋白质合成调控的工具。

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本文引用的文献

1
A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPY.一种用于电子显微镜的简化柠檬酸铅染色法。
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Effects of testosterone on protein synthesis in rat seminal vesicles analysed by two-dimensional gel electrophoresis.
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Sperm-coating antigens secreted by the epididymis and seminal vesicle of the rat.
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Effect of castration on the synthesis of seminal vesicle secretory protein IV in the rat.去势对大鼠精囊分泌蛋白IV合成的影响。
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Development of secretory protein synthesis in the seminal vesicles and ventral prostate of the male rat.雄性大鼠精囊和腹侧前列腺中分泌蛋白合成的发育
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Sizing of protein A-colloidal gold probes for immunoelectron microscopy.用于免疫电子显微镜的蛋白A-胶体金探针的大小测定
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Seminal vesicle secretion IV gene: allelic difference due to a series of 20-base-pair direct tandem repeats within an intron.精囊分泌IV基因:由于内含子内一系列20个碱基对的直接串联重复序列导致的等位基因差异。
Proc Natl Acad Sci U S A. 1983 Nov;80(21):6460-4. doi: 10.1073/pnas.80.21.6460.
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Isolation and culture of rat seminal vesicle epithelial cells. The use of the secretory protein SVS IV as a functional probe.大鼠精囊上皮细胞的分离与培养。使用分泌蛋白SVS IV作为功能探针。
Exp Cell Res. 1983 May;145(2):293-304. doi: 10.1016/0014-4827(83)90008-3.
9
The seminal vesicle secretion IV gene: detection of S1 nuclease-sensitive sites in supercoiled plasmid pSVS 3.3.精囊分泌IV基因:超螺旋质粒pSVS 3.3中S1核酸酶敏感位点的检测
DNA. 1983;2(2):105-11. doi: 10.1089/dna.1983.2.105.
10
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