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小鼠精子上一种精液蛋白酶抑制剂-透明带结合成分的特征

Features of a seminal proteinase inhibitor- zona pellucida-binding component on murine spermatozoa.

作者信息

Robinson R, Richardson R, Hinds K, Clayton D, Poirier G R

机构信息

Department of Biology, University of Alabama 35294.

出版信息

Gamete Res. 1987 Mar;16(3):217-28. doi: 10.1002/mrd.1120160304.

Abstract

Murine cauda epididymal sperm contain sites on the plasma membrane over the apical portion of the acrosome that recognize proteinase inhibitors and the homologous zona pellucida. Ten times more of the component can be extracted from cauda and ductus sperm than from equal numbers of caput and corpus sperm. Likewise, few sperm from the upper epididymal regions are able to bind seminal inhibitor, while the majority of sperm from the cauda and ductus do bind. Cauda epididymal and ductus sperm lose little of their ability to bind inhibitor after a 4-hour in vitro incubation in either a capacitating or a noncapacitating medium. The percentage of naturally inseminated sperm with the seminal inhibitor bound to their surface decreases to about 10 after 4 hours in utero. Approximately 80% of these sperm show positive fluorescence when given the opportunity to rebind the the inhibitor, and these sperm do have an intact plasma membrane over the apical portion of the acrosome. Furthermore, after 4 hours in utero, the inhibitor bound in the same region of the sperm head as it did on freshly ejaculated sperm. The seminal inhibitor inhibits the binding of sperm to the zona if added during the first 15 minutes of incubation but has no effect on attachment. The data indicate that sperm gain the ability to bind the seminal inhibitor during the epididymal sojourn. Furthermore, this binding capacity is not lost during in vitro or in utero incubation. The site is not involved in sperm-zona attachment but does participate in the binding of sperm to the zona.

摘要

小鼠附睾尾部精子的顶体部质膜上存在能识别蛋白酶抑制剂和同源透明带的位点。从附睾尾部和输精管精子中提取的该成分比从等量的附睾头部和体部精子中提取的多10倍。同样,来自附睾上部区域的精子很少能结合精液抑制剂,而来自附睾尾部和输精管的大多数精子则能结合。附睾尾部和输精管精子在获能或非获能培养基中体外孵育4小时后,其结合抑制剂的能力几乎没有丧失。自然受精的精子表面结合精液抑制剂的比例在子宫内4小时后降至约10%。当有机会重新结合抑制剂时,这些精子中约80%显示阳性荧光,并且这些精子在顶体部有完整的质膜。此外,在子宫内4小时后,抑制剂结合在精子头部的同一区域,就像在新鲜射出的精子上一样。如果在孵育的前15分钟加入精液抑制剂,它会抑制精子与透明带的结合,但对附着没有影响。数据表明,精子在附睾停留期间获得了结合精液抑制剂的能力。此外,这种结合能力在体外或子宫内孵育期间不会丧失。该位点不参与精子与透明带的附着,但确实参与精子与透明带的结合。

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