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Liposomes for cryopreservation of bovine sperm

机译:冻存牛精子的脂质体

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In this study, the effect of various unilamellar liposomes on cryopreservation of bovine spermatozoa has been investigated. Liposomes were composed of saturated lipids with various acyl chain lengths: DSPC (18:0), DPPC (16:0), DMPC (14:0), or DLPC (12:0). Alternatively, liposomes were prepared using unsaturated egg phosphatidylcholine (EPC) or DOPC (18:1, neutral), alone or in combination with lipids with various head groups: DOPS (negatively charged), DOPG (negatively charged), and DOPE (neutral). Fourier transform infrared spectroscopy studies showed that bovine sperm membranes display a gradual phase transition from 10 to 24 degrees C. Phase transition temperatures of the liposomes varied from -20 to +53 degrees C. Sperm was incubated in the presence of liposomes for either 6 or 24 h at 4 degrees C prior to freezing. Postfreeze survival rates were determined based on the percentage of progressively motile cells as well as the percentage of acrosome- and plasma membrane-intact cells. With DOPC liposomes a postthaw progressive motility of 43% was obtained compared with 59% using standard egg yolk freezing extender. Postthaw progressive motility increased up to 52% using DOPC:DOPG (9:1) liposomes, whereas DOPC:DOPS or DOPC:DOPE liposomes did not increase survival compared with DOPC liposomes. Among the saturated lipids, only DMPC was found to increase cryosurvival, up to 44% based on progressive motility. DLPC liposomes caused a complete loss in cell viability, already prior to freezing, whereas DPPC and DSPC liposomes neither positively nor negatively affected cryosurvival. Taken together, the higher postthaw survival obtained with DOPC:DOPG liposomes as compared with DOPC liposomes can likely be attributed to increased liposome-sperm interactions between the charged phosphatidylglycerol groups and charged regions in the sperm membranes. Interestingly, the lipid phase state of the liposomes during preincubation is not the decisive factor for their cryoprotective action
机译:在这项研究中,已研究了各种单层脂质体对牛精子冷冻保存的影响。脂质体由具有各种酰基链长度的饱和脂质组成:DSPC(18:0),DPPC(16:0),DMPC(14:0)或DLPC(12:0)。或者,脂质体可使用不饱和卵磷脂酰胆碱(EPC)或DOPC(18:1,中性)单独或与具有不同首基的脂质组合使用:DOPS(带负电),DOPG(带负电)和DOPE(中性) 。傅里叶变换红外光谱研究表明,牛精子膜显示出从10到24摄氏度的逐渐相变。脂质体的相变温度从-20到+53摄氏度不等。将精子在脂质体存在下孵育6或7℃。冷冻前在4摄氏度下放置24小时。冻结后的存活率是根据渐进运动细胞的百分比以及顶体和质膜完整细胞的百分比确定的。使用DOPC脂质体后,解冻后进行性运动率为43%,而使用标准蛋黄冷冻增量剂为59%。与DOPC脂质体相比,使用DOPC:DOPG(9:1)脂质体后融化后的运动能力提高了52%,而DOPC:DOPS或DOPC:DOPE脂质体并未增加存活率。在饱和脂质中,仅DMPC被发现可提高冷冻存活率,基于进行性运动可高达44%。冷冻前,DLPC脂质体已引起细胞活力的完全丧失,而DPPC和DSPC脂质体既没有正面影响,也没有负面影响冷冻存活。两者合计,与DOPC脂质体相比,DOPC:DOPG脂质体获得的更高的解冻后存活率可能归因于带电的磷脂酰甘油基团与精子膜中带电区域之间脂质体-精子相互作用的增加。有趣的是,预孵育过程中脂质体的脂质相状态不是其防冻作用的决定性因素

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