Department of Animal Sciences and Institute of Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Division of Animal Sciences, University of Missouri, Columbia, Missouri, USA.
Reproduction. 2021 Apr;161(4):449-457. doi: 10.1530/REP-20-0474.
In mammals, the oviduct retains sperm, forming a reservoir from which they are released in synchrony with ovulation. However, the mechanisms underlying sperm release are unclear. Herein, we first examined in greater detail the release of sperm from the oviduct reservoir by sex steroids, and secondly, if the ubiquitin-proteasome system (UPS) mediates this release in vitro. Sperm were allowed to bind to oviductal cells or immobilized oviduct glycans, either bi-SiaLN or a suLeX, and channeled with steroids in the presence or absence of proteasome inhibitors. Previously, we have demonstrated progesterone-induced sperm release from oviduct cells and immobilized glycans in a steroid-specific manner. Herein, we found that the release of sperm from an immobilized oviduct glycan, a six-sialylated branched structure, and from immobilized fibronectin was inhibited by the CatSper blocker NNC 055-0396, akin to the previously reported ability of NNC 055-0396 to inhibit sperm release from another oviduct glycan, sulfated Lewis-X trisaccharide. Thus, CatSper may be required for release of sperm from a variety of adhesion systems. One possible mechanism for sperm release is that glycan receptors on sperm are degraded by proteasomes or shed from the sperm surface by proteasomal degradation. Accordingly, the inhibition of proteasomal degradation blocked sperm release from oviduct cell aggregates both immobilized oviduct glycans as well as fibronectin. In summary, progesterone-induced sperm release requires both active CatSper channels and proteasomal degradation, suggesting that hyperactivation and proteolysis are vital parts of the mechanism by which sperm move from the oviduct reservoir to the site of fertilization.
在哺乳动物中,输卵管保留精子,形成一个储存库,精子从中同步释放,与排卵同步。然而,精子释放的机制尚不清楚。在此,我们首先更详细地检查了性类固醇对输卵管储存库中精子释放的影响,其次,如果泛素-蛋白酶体系统 (UPS) 介导了这种体外释放。允许精子与输卵管细胞或固定的输卵管糖结合,无论是双唾液酸化 LN 还是 suLeX,并在存在或不存在蛋白酶体抑制剂的情况下用类固醇进行通道化。以前,我们已经证明孕激素以类固醇特异性的方式诱导输卵管细胞和固定糖从精子中释放。在此,我们发现,从固定的输卵管糖,即六唾液酸化分支结构,以及从固定的纤维连接蛋白中释放精子被 CatSper 阻滞剂 NNC 055-0396 抑制,类似于以前报道的 NNC 055-0396 抑制另一种输卵管糖,硫酸化 Lewis-X 三糖的精子释放的能力。因此,CatSper 可能是精子从各种粘附系统释放所必需的。精子释放的一种可能机制是,精子上的糖受体被蛋白酶体降解,或者通过蛋白酶体降解从精子表面脱落。因此,蛋白酶体降解的抑制阻断了输卵管细胞聚集体中固定的输卵管糖以及纤维连接蛋白的精子释放。总之,孕激素诱导的精子释放需要活性 CatSper 通道和蛋白酶体降解,这表明超活化和蛋白水解是精子从输卵管储存库移动到受精部位的机制的重要组成部分。