Hermansson Ulrika, Axnér Eva, Holst Bodil Ström
Department of Clinical Sciences, Division of Diagnostic Imaging and Clinical Pathology, Swedish University of Agricultural Sciences (SLU), Box 7054, SE-750 07 Uppsala, Sweden.
Acta Vet Scand. 2007 Oct 1;49(1):28. doi: 10.1186/1751-0147-49-28.
Zona pellucida binding assays (ZBAs) have proven useful in determining the fertilising ability of spermatozoa in several species. Most ZBAs use fresh or salt-stored oocytes collected from fresh ovaries but because ovaries are not easy to obtain on a regular basis, chilled and frozen-thawed ovaries have been tested, with varying results. The present study tested the hypothesis that cat spermatozoa, either fresh or frozen-thawed, can bind to homologous zona pellucida of oocytes retrieved from frozen-thawed queen ovaries to a similar extent as they can bind to the zona pellucida of fresh, in vitro matured oocytes.
Ovaries were collected from queens after routine ovario-hysterectomy and either stored in NaCl at -20 degrees C until use (treatment animals), or used fresh (controls). Cumulus-oocyte complexes (COCs) were retrieved by ovarian slicing from either source and used directly (immature oocytes from frozen-thawed ovaries; treatment animals) or after in vitro maturation (IVM) (fresh ovaries; controls) for 24 hours in TCM 199, supplemented with 1 IU hCG/mL and 0.5 IU eCG/mL and 0.5% bovine serum albumin (BSA). The oocytes were incubated for 4 hours in 5% CO2 in air at 38 degrees C and 100% humidity in the presence of 5 x 106 fresh or frozen-thawed spermatozoa/mL. Representative samples of oocytes were processed for scanning electron microscopy (SEM).
Both fresh and frozen-thawed spermatozoa bound to the in vitro matured zona pellucida but significantly fewer, or no, spermatozoa bound to frozen-thawed, immature zona pellucida (P < 0.001). Also, more fresh spermatozoa than frozen-thawed spermatozoa bound to the zona pellucida (P < 0.001). The zona pellucida surface differed in morphology (SEM), with in vitro matured oocytes showing a dense surface with few fenestrations in contrast to their frozen-thawed, immature counterparts, where fenestrations were conspicuously larger.
In conclusion, under the conditions of the present study, immature oocytes recovered from ovaries frozen immersed in NaCl at -20 degrees C are less suitable for use in feline ZBA.
透明带结合试验(ZBAs)已被证明在确定几种物种精子的受精能力方面很有用。大多数透明带结合试验使用从新鲜卵巢收集的新鲜或盐储存的卵母细胞,但由于卵巢不容易定期获得,已对冷冻和冻融的卵巢进行了测试,结果各不相同。本研究检验了以下假设:新鲜或冻融的猫精子与从冻融的母猫卵巢中获取的卵母细胞的同源透明带结合的程度,与它们与新鲜的、体外成熟的卵母细胞的透明带结合的程度相似。
在常规卵巢子宫切除术后从母猫收集卵巢,要么在-20℃的氯化钠中储存直至使用(处理组动物),要么新鲜使用(对照组)。通过卵巢切片从任一来源获取卵丘-卵母细胞复合体(COCs),直接使用(来自冻融卵巢的未成熟卵母细胞;处理组动物)或在补充有1 IU hCG/mL、0.5 IU eCG/mL和0.5%牛血清白蛋白(BSA)的TCM 199中体外成熟(IVM)24小时后使用(新鲜卵巢;对照组)。将卵母细胞在38℃、含5%二氧化碳的空气和100%湿度条件下,在每毫升含5×106个新鲜或冻融精子的情况下孵育4小时。对代表性的卵母细胞样本进行扫描电子显微镜(SEM)处理。
新鲜和冻融的精子均能与体外成熟的透明带结合,但与冻融的未成熟透明带结合的精子明显较少或不结合(P < 0.001)。此外,与冻融精子相比,更多的新鲜精子与透明带结合(P < 0.001)。透明带表面在形态上有所不同(SEM),体外成熟的卵母细胞表面致密,开窗较少,而冻融的未成熟卵母细胞的开窗明显更大。
总之,在本研究条件下,从-20℃氯化钠中冷冻浸泡的卵巢中回收的未成熟卵母细胞不太适合用于猫的透明带结合试验。