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推测曼氏血吸虫雄性向雌性的多肽转移。

Putative polypeptide transfer from male to female Schistosoma mansoni.

作者信息

Popiel I, Basch P F

出版信息

Mol Biochem Parasitol. 1984 Apr;11:179-88. doi: 10.1016/0166-6851(84)90064-1.

DOI:10.1016/0166-6851(84)90064-1
PMID:6749178
Abstract

Mature males and females, and unisexual females of Schistosoma mansoni were incubated in medium containing [14C]leucine. By use of polyacrylamide gel electrophoresis and fluorography no differences were detected in their ability to synthesize polypeptides. Male worms thus labelled were paired for various periods with unlabelled mature or unisexual females both in vitro and by surgical implantation into hamsters. Female worms paired in vitro had two controls: an accompanying female that did not pair and an additional female placed in the conditioned medium after removal of the other worms. After separation and washing, only small amounts of label were found in females by liquid scintillation counting despite the release by males of substantial amounts of label into the medium. No label was detected in fluorograms of polyacrylamide electrophoresis gels of re-paired females after 7 days' exposure to X-ray film, but a faint pattern of normal polypeptides above 50 kDa did develop after 6 weeks. In light microscope autoradiographs a low grain count was found over sections of unlabelled females paired with labelled males but this was no greater than that over females incubated in medium that had formerly held males. We have been unable to detect any polypeptide reported to be synthesized exclusively by male worms and transferred in large amounts to females. Although female worms did take up small amounts of male-derived metabolic products, the transfer of a specific polypeptide of 66 kDa in significant quantities did not take place under the conditions investigated.

摘要

将曼氏血吸虫的成熟雄虫和雌虫以及孤雌生殖雌虫置于含有[14C]亮氨酸的培养基中培养。通过聚丙烯酰胺凝胶电泳和荧光自显影法,未检测到它们在合成多肽能力上的差异。用这种方法标记的雄虫,在体外以及通过手术植入仓鼠体内的方式,与未标记的成熟雌虫或孤雌生殖雌虫配对不同时长。体外配对的雌虫有两个对照:一个未配对的伴雌,以及在移除其他虫体后置于条件培养基中的另一只雌虫。分离并洗涤后,尽管雄虫向培养基中释放了大量标记物,但通过液体闪烁计数法在雌虫中仅发现少量标记物。重新配对的雌虫聚丙烯酰胺电泳凝胶的荧光自显影片在X射线胶片曝光7天后未检测到标记,但在6周后确实出现了50 kDa以上正常多肽的微弱图谱。在光学显微镜放射自显影片中,未标记的雌虫与标记雄虫配对的切片上发现的颗粒计数较低,但这并不比在曾放置过雄虫的培养基中培养的雌虫切片上的颗粒计数高。我们未能检测到任何据报道仅由雄虫合成并大量转移至雌虫的多肽。尽管雌虫确实摄取了少量源自雄虫的代谢产物,但在所研究的条件下,并未发生大量转移特定的66 kDa多肽的情况。

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