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朊病毒蛋白以可溶形式分泌于附睾液中,并在精浆中进行蛋白水解加工和运输。

Prion protein is secreted in soluble forms in the epididymal fluid and proteolytically processed and transported in seminal plasma.

作者信息

Gatti Jean-Luc, Métayer Sonia, Moudjou Mohammed, Andréoletti Olivier, Lantier Frédéric, Dacheux Jean-Louis, Sarradin Pierre

机构信息

Equipe Spermatozoïdes, Station de Pathologie Infectieuse et Immunologie, Institut National de la Recherche Agronomique, INRA Nouzilly, 37380 Monnaie, France.

出版信息

Biol Reprod. 2002 Aug;67(2):393-400. doi: 10.1095/biolreprod67.2.393.

Abstract

The presence of prion protein in sperm and fluids collected from different parts of the ram genital tract was investigated by immunoblotting with monoclonal antibodies. A slightly immunoreactive 25- to 30-kDa protein was recognized on Western blots of testicular and epididymal sperm extracts. Immunoreactivity increased on ejaculated sperm extracts and 2 other bands at 35 and 43 kDa also reacted. Seminal plasma showed several immunoreactive bands, the main bands being detected at 43 and 35 kDa, whereas less reactive bands were observed at 30, 25, 20, and <14 kDa. All these bands strongly decreased in the seminal plasma after vasectomy, indicating a testicular or an epididymal origin. Testicular fluid showed almost no reactivity, whereas caudal epididymal fluid contained the 2 strong immunoreactive bands at 43 and 35 kDa and in some cases a faint 30-kDa band. The 43-kDa band was also found in the fluid from the proximal caput, whereas the 35-kDa band appeared in the distal caput. Immunoprecipitation of (35)S-labeled proteins secreted in the epididymal fluid indicated that the 43-kDa form was synthesized in caput and caudal regions and the 35-kDa form in the distal caput to the distal corpus. Treatment of caudal fluid and seminal plasma by N-glycosidase resulted in the formation of 3 bands: 1 highly reactive at about 25 kDa, a second less reactive at about 28 kDa, and a third at approximately 20 kDa. The pattern of prion protein distribution in epididymal fluids was found to be similar in scrapie-infected rams to that of healthy rams. Cauda epididymal fluid and seminal plasma from infected animals could not be treated directly with proteinase K, because of the presence of protease inhibitors. However, the prion protein immunoprecipitated from these fluids was completely cleaved by proteinase K, whereas in the same conditions this from an infected sheep brain gave the usual resistant band pattern.

摘要

采用单克隆抗体免疫印迹法,研究了从公羊生殖道不同部位采集的精子和精液中朊病毒蛋白的存在情况。在睾丸和附睾精子提取物的蛋白质免疫印迹中,识别出一种略有免疫反应性的25至30 kDa蛋白质。射精精子提取物的免疫反应性增强,并且在35 kDa和43 kDa处的另外两条带也发生反应。精浆显示出几条免疫反应带,主要条带在43 kDa和35 kDa处检测到,而在30 kDa、25 kDa、20 kDa和<14 kDa处观察到反应较弱的条带。输精管结扎后,精浆中所有这些条带的反应性均大幅下降,表明其起源于睾丸或附睾。睾丸液几乎没有反应性,而附睾尾液含有43 kDa和35 kDa处的两条强免疫反应带,在某些情况下还有一条微弱的30 kDa条带。在附睾头近端的液体中也发现了43 kDa条带,而35 kDa条带出现在附睾头远端。对附睾液中分泌的(35)S标记蛋白进行免疫沉淀表明,43 kDa形式在附睾头和附睾尾区域合成,35 kDa形式在附睾头远端至附睾体远端合成。用N-糖苷酶处理附睾尾液和精浆后形成三条带:一条在约25 kDa处反应性高,第二条在约28 kDa处反应性较低,第三条在约20 kDa处反应性较低。发现瘙痒病感染公羊附睾液中朊病毒蛋白的分布模式与健康公羊相似。由于存在蛋白酶抑制剂,感染动物的附睾尾液和精浆不能直接用蛋白酶K处理。然而,从这些液体中免疫沉淀的朊病毒蛋白被蛋白酶K完全切割,而在相同条件下,来自感染绵羊大脑的朊病毒蛋白呈现出通常的抗性条带模式。

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