Poirier G R, Nicholson N
J Exp Zool. 1984 Jun;230(3):465-71. doi: 10.1002/jez.1402300315.
Monoclonal antibodies to a low molecular weight, acid-stable acrosin-trypsin inhibitor isolated from epididymal homogenates were used to localize the inhibitor in tissues and secretions of the male reproductive tract of mice. The inhibitor, identified by indirect immunofluorescence, is present in the testes and in the apical portion of the epithelial cells from the caput region of the epididymis of both intact and efferentiectomized animals. Sperm isolated from the testes and caput epididymal region show inhibitor-positive fluorescence on the anterior acrosomal region. The inhibitor could not be localized on ductus or electroejaculated sperm or ductus sperm previously incubated in a purified inhibitor solution. Furthermore, the inhibitor was not visible in the copulatory plug of recently inseminated animals or on sperm recovered from the uterus or from an artificial capacitating medium. The inhibitor could be detected by an enzyme-linked immunosorbent assay in the supernatants of detergent treated or frozen-thawed caput sperm but not of ductus sperm. The data suggest that the inhibitor, made in both the testes and caput epididymis where it associates with the sperm, is lost from the sperm or irreversibly masked during the epididymal sojourn.
利用从附睾匀浆中分离出的一种低分子量、酸稳定的顶体蛋白酶 - 胰蛋白酶抑制剂的单克隆抗体,在小鼠雄性生殖道的组织和分泌物中定位该抑制剂。通过间接免疫荧光鉴定,该抑制剂存在于完整和去输出管动物附睾头区域的睾丸和上皮细胞顶端部分。从睾丸和附睾头区域分离的精子在前顶体区域呈现抑制剂阳性荧光。在输精管或电刺激射精的精子上,或在先前在纯化抑制剂溶液中孵育过的输精管精子上,均未检测到该抑制剂。此外,在近期授精动物的交配栓中,或从子宫或人工获能培养基中回收的精子上,也未见到该抑制剂。通过酶联免疫吸附测定法可在经去污剂处理或冻融的附睾头精子的上清液中检测到该抑制剂,但在输精管精子的上清液中未检测到。数据表明,在睾丸和附睾头中产生并与精子结合的该抑制剂,在附睾停留期间从精子上丢失或被不可逆地掩盖。