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家畜附睾液中一种分子量为105至94千道尔顿的蛋白质是血管紧张素I转换酶(ACE);有证据表明精子是这种ACE的来源。

A 105- to 94-kilodalton protein in the epididymal fluids of domestic mammals is angiotensin I-converting enzyme (ACE); evidence that sperm are the source of this ACE.

作者信息

Gatti J L, Druart X, Guérin Y, Dacheux F, Dacheux J L

机构信息

URA 1291 INRA-CNRS, Institut National de la Recherche Agronomique, Station de Physiologie de la Reproduction des Mammifères Domestiques, 37380 Monnaie,

出版信息

Biol Reprod. 1999 Apr;60(4):937-45. doi: 10.1095/biolreprod60.4.937.

Abstract

SDS-PAGE analysis of luminal fluid from the ram testis and epididymis revealed a protein of about 105 kDa in the fluid in the caput epididymal region. The molecular mass of this fluid protein shifted from 105 kDa to 94 kDa in the distal caput epididymidis and remained at 94 kDa in the lower regions of the epididymis. The possible sperm origin of this protein was suggested by the decrease in intensity of a 105-kDa compound on the sperm plasma membrane extract and by its total disappearance from the fluid of animals with impaired sperm production caused by scrotal heating. The 94-kDa protein was purified from ram cauda epididymal fluid, and a rabbit polyclonal antiserum was obtained. This antiserum showed that membranes of testicular sperm and sperm from the initial caput were positive for the presence of an immunologically related antigen. The protein was immunolocalized mainly on the flagellar intermediate piece, whereas in some corpus and caudal sperm, only the apical ridge of the acrosomal vesicle was labeled. The purified protein was microsequenced: its N-terminal was not found in the sequence database, but its tryptic fragments matched the sequence of the angiotensin I-converting enzyme (ACE). Indeed, the purified 94-kDa protein exhibited a carboxypeptidase activity inhibited by specific blockers of ACE. All the soluble seminal plasma ACE activity in the ram was attributable to the 94-kDa epididymal fluid ACE. The polyclonal antiserum also showed that a soluble form of ACE appeared specifically in the caput epididymal fluid of the boar, stallion, and bull. This soluble form was responsible for all the ACE activity observed in the fluid from the distal caput to the cauda epididymidis in these species. Our results strongly suggest that the epididymal fluid ACE derives from the germinal form of ACE that is liberated from the testicular sperm in a specific epididymal area.

摘要

对公羊睾丸和附睾管腔液进行的SDS - PAGE分析显示,在附睾头区域的液体中有一种约105 kDa的蛋白质。这种液体蛋白的分子量在附睾头远端从105 kDa转变为94 kDa,并在附睾下部区域保持在94 kDa。精子质膜提取物上105 kDa化合物强度的降低以及阴囊加热导致精子生成受损的动物的液体中该化合物完全消失,提示了这种蛋白质可能来源于精子。从公羊附睾尾液中纯化出了94 kDa的蛋白质,并获得了兔多克隆抗血清。该抗血清显示,睾丸精子和附睾头起始段精子的膜上存在免疫相关抗原呈阳性。该蛋白质主要免疫定位在鞭毛中间段,而在一些附睾体和附睾尾精子中,仅顶体泡的顶嵴被标记。对纯化的蛋白质进行了微量测序:其N端未在序列数据库中找到,但其胰蛋白酶片段与血管紧张素I转换酶(ACE)的序列匹配。实际上,纯化的94 kDa蛋白质表现出被ACE特异性阻滞剂抑制的羧肽酶活性。公羊精液中所有可溶性精浆ACE活性都归因于94 kDa的附睾液ACE。多克隆抗血清还显示,可溶性形式的ACE特异性出现在公猪、种马和公牛的附睾头液中。这种可溶性形式负责在这些物种中从附睾头远端到附睾尾的液体中观察到的所有ACE活性。我们的结果强烈表明,附睾液ACE来源于在特定附睾区域从睾丸精子释放的ACE的生殖形式。

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