Kew D, Muffly K E, Kilpatrick D L
Neurobiology Group, Worcester Foundation for Experimental Biology, Shrewsbury, MA 01545.
Proc Natl Acad Sci U S A. 1990 Dec;87(23):9143-7. doi: 10.1073/pnas.87.23.9143.
Previous studies have shown that spermatogenic cells are a major source of testicular RNA encoding the opioid peptide precursor proenkephalin, suggesting that proenkephalin-derived peptides may function as intratesticular paracrine factors produced by male germ cells. However, direct evidence for the production of proenkephalin by spermatogenic cells has been lacking. In this report, we have used polysome profile analysis, peptide quantitation, and immunocytochemistry to show that proenkephalin products are synthesized during spermatogenesis and are retained within spermatozoa of humans, hamsters, rats, and sheep. We further show that these peptides are stored in the sperm acrosome and are depleted from sperm following the acrosome reaction, an exocytotic event required for fertilization. Proenkephalin products thus may serve a dual function as sperm acrosomal factors released during the fertilization process as well as intratesticular regulators secreted by spermatogenic cells.
先前的研究表明,生精细胞是睾丸中编码阿片肽前体脑啡肽原的RNA的主要来源,这表明脑啡肽原衍生的肽可能作为雄性生殖细胞产生的睾丸内旁分泌因子发挥作用。然而,一直缺乏生精细胞产生脑啡肽原的直接证据。在本报告中,我们使用多核糖体谱分析、肽定量和免疫细胞化学来表明,脑啡肽原产物在精子发生过程中合成,并保留在人类、仓鼠、大鼠和绵羊的精子内。我们进一步表明,这些肽储存在精子顶体中,并在顶体反应(受精所需的胞吐事件)后从精子中耗尽。因此,脑啡肽原产物可能具有双重功能,既是受精过程中释放的精子顶体因子,也是生精细胞分泌的睾丸内调节剂。