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12千道尔顿的FK506结合蛋白FKBP12在雄性生殖道中释放,并刺激精子活力。

The 12 kD FK 506 binding protein FKBP12 is released in the male reproductive tract and stimulates sperm motility.

作者信息

Walensky L D, Dawson T M, Steiner J P, Sabatini D M, Suarez J D, Klinefelter G R, Snyder S H

机构信息

Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Mol Med. 1998 Aug;4(8):502-14.

Abstract

BACKGROUND

The 12 kD FK506 binding protein FKBP12 is a cytosolic receptor for the immunosuppressant drugs FK506 and rapamycin. In addition to its critical role in drug-induced T-cell immunosuppression, FKBP12 associates physiologically with ryanodine and inositol 1,4,5-trisphosphate (IP3) receptors, regulating their ability to flux calcium. We investigated a role for FKBP12 in male reproductive physiology on the basis of our identification of extremely high levels of [3H]FK506 binding in male reproductive tissues.

MATERIALS AND METHODS

[3H]FK506 binding studies were performed to identify tissues enriched with FK506 binding sites. The abundant [3H]FK506 binding sites identified in the male reproductive tract were localized by [3H]FK506 autoradiography. FK506 affinity chromatography was employed to purify FKBP from epididymal fluid. Anti-FKBP12 Western analysis was used to confirm the identity of the purified FKBP. The binding of exogenous FKBP12 to sperm was evaluated by [32P]FKBP12 binding studies and [33P]FKBP12 autoradiography. The effect of recombinant FKBP12 on sperm motility was investigated using a Hamilton Thorne motility analyzer.

RESULTS

Male reproductive tissues contained high levels of [3H]FK506 binding. The localization of [3H]FK506 binding sites to the tubular epithelium of the caput epididymis and the lumen of the cauda and vas deferens suggested that FKBP is released in the male reproductive tract. FKBP12 was purified from epididymal plasma by FK506 affinity chromatography. Radiolabeled FKBP12 specifically bound to immature but not mature sperm. In sperm motility studies, FKBP12-treated caput sperm exhibited double the curvilinear velocity of untreated controls.

CONCLUSIONS

High levels of FKBP12 are released in the male reproductive tract and specifically associate with maturing sperm. Recombinant FKBP12 enhances the curvilinear velocity of immature sperm, suggesting a role for FKBP12 in motility initiation. The highest concentrations of soluble FKBP12 in the male reproductive tract occur in the lumen of the vas deferens, a site of sperm storage and the conduit for ejaculated sperm. Preservation of mammalian sperm for reproductive technologies may be optimized by supplementing incubation or storage media with FKBP12.

摘要

背景

12kD的FK506结合蛋白FKBP12是免疫抑制剂FK506和雷帕霉素的胞质受体。除了在药物诱导的T细胞免疫抑制中起关键作用外,FKBP12在生理上还与ryanodine和肌醇1,4,5-三磷酸(IP3)受体相关联,调节它们的钙通量能力。基于我们在雄性生殖组织中发现极高水平的[3H]FK506结合,我们研究了FKBP12在雄性生殖生理学中的作用。

材料与方法

进行[3H]FK506结合研究以鉴定富含FK506结合位点的组织。通过[3H]FK506放射自显影法对在雄性生殖道中鉴定出的丰富的[3H]FK506结合位点进行定位。采用FK506亲和层析从附睾液中纯化FKBP。使用抗FKBP12 Western分析来确认纯化的FKBP的身份。通过[32P]FKBP12结合研究和[33P]FKBP12放射自显影法评估外源性FKBP12与精子的结合。使用Hamilton Thorne运动分析仪研究重组FKBP12对精子活力的影响。

结果

雄性生殖组织含有高水平的[3H]FK506结合。[3H]FK506结合位点定位于附睾头的管状上皮以及附睾尾和输精管的管腔,这表明FKBP在雄性生殖道中释放。通过FK506亲和层析从附睾血浆中纯化出FKBP12。放射性标记的FKBP12特异性结合未成熟但不结合成熟精子。在精子活力研究中,经FKBP12处理的附睾头精子的曲线速度是未处理对照的两倍。

结论

高水平的FKBP12在雄性生殖道中释放,并特异性地与成熟精子相关联。重组FKBP12提高未成熟精子的曲线速度,表明FKBP12在活力启动中起作用。雄性生殖道中可溶性FKBP12的最高浓度出现在输精管管腔中,输精管是精子储存部位和射精精子的通道。通过在孵育或储存培养基中补充FKBP12,可能会优化用于生殖技术的哺乳动物精子的保存。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248d/2230403/b5dca283684f/molmed00020-0021-a.jpg

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