Boilard M, Reyes-Moreno C, Lachance C, Massicotte L, Bailey J L, Sirard M-A, Leclerc P
Département des Sciences Animales, Centre de Recherche en Biologie de la Reproduction, Université Laval, Québec, QC, Canada G1K 7P4.
Biol Reprod. 2004 Dec;71(6):1879-89. doi: 10.1095/biolreprod.103.026849. Epub 2004 Jul 30.
Upon their transit through the female genital tract, bovine spermatozoa bind to oviduct epithelial cells, where they are maintained alive for long periods of time until fertilization. Although carbohydrate components of the oviduct epithelial cell membrane are involved in these sperm/oviduct interactions, no protein candidate has been identified to play this role. To identify the oviduct factors involved in their survival, sperm cells were preincubated for 30 min with apical membranes isolated from oviduct epithelial cells, washed extensively, and further incubated for up to 12 h in the absence of apical membranes. During this incubation, sperm viability, motility, and acrosomal integrity were improved compared with cells preincubated in the absence of apical membranes. This suggests that, during the 30-min preincubation with apical membrane extracts, either an oviductal factor triggered intracellular events resulting in positive effects on spermatozoa or that such a factor strongly attached to sperm cells to promote a positive action. Similarly, spermatozoa were incubated with apical membranes isolated from oviduct epithelial cells labeled with [35S]-methionine and, upon extensive washes, proteins were separated by two-dimensional (2-D) gel electrophoresis to identify the factors suspected to have beneficial effects on spermatozoa. The six major proteins, according to their signal intensity on the autoradiographic film, were extracted from a 2-D gel of oviduct epithelial cell proteins run in parallel and processed for N-terminal sequencing of the first 15 amino acids. Of these, one was identical to heat shock protein 60 (HSP60) and one to the glucose-regulated protein 78 (GRP78). Their identities and association with spermatozoa were confirmed using an antibody directed against these proteins. This paper reports the localization of both GRP78 and HSP60 on the luminal/apical surface of oviduct epithelial cells, their binding to spermatozoa, and the presence of endogenous HSP60 in the sperm midpiece.
在穿过雌性生殖道的过程中,牛精子会与输卵管上皮细胞结合,在那里它们可以长时间保持存活状态,直至受精。虽然输卵管上皮细胞膜的碳水化合物成分参与了这些精子与输卵管的相互作用,但尚未鉴定出发挥这一作用的蛋白质候选物。为了确定参与精子存活的输卵管因子,精子细胞先与从输卵管上皮细胞分离的顶端膜预孵育30分钟,充分洗涤后,在无顶端膜的情况下进一步孵育长达12小时。在该孵育过程中,与未用顶端膜预孵育的细胞相比,精子活力、运动能力和顶体完整性均得到改善。这表明,在与顶端膜提取物预孵育的30分钟内,要么是一种输卵管因子触发了细胞内事件,从而对精子产生积极影响,要么是这样一种因子强烈附着于精子细胞以促进积极作用。同样,将精子与用[35S]-甲硫氨酸标记的输卵管上皮细胞分离的顶端膜一起孵育,经过充分洗涤后,通过二维(2-D)凝胶电泳分离蛋白质,以鉴定怀疑对精子有有益作用的因子。根据放射自显影片上的信号强度,从平行运行的输卵管上皮细胞蛋白质的2-D凝胶中提取六种主要蛋白质,并对其前15个氨基酸进行N端测序。其中,一种与热休克蛋白60(HSP60)相同,另一种与葡萄糖调节蛋白78(GRP78)相同。使用针对这些蛋白质的抗体证实了它们的身份以及与精子的关联。本文报道了GRP78和HSP60在输卵管上皮细胞腔面/顶端表面的定位、它们与精子的结合以及精子中段中内源性HSP60的存在。