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微流控精子分选器在猪卵母细胞体外受精中的应用降低了多精穿透的发生率。

Application of a microfluidic sperm sorter to the in-vitro fertilization of porcine oocytes reduced the incidence of polyspermic penetration.

机构信息

Department of Animal Science, Graduate School of Natural Science and Technology, Okayama University, Kita-Ku, Okayama, Japan.

出版信息

Theriogenology. 2010 Sep 15;74(5):863-70. doi: 10.1016/j.theriogenology.2010.04.011. Epub 2010 May 26.

Abstract

The objective of this study was to use a microfluidic sperm sorter (MFSS), designed to isolate motile human spermatozoa with laminar flows (no centrifugation), for porcine IVF. Boar spermatozoa were diluted at 1 x 10(8) cells/mL with a diluent containing 20% seminal fluid and flowed with modified TCM-199 (mM199, with 5 mM caffeine) to introduce motile sperm into the exit chamber for IVF. In Experiment 1, after flowing for 5 min, sperm concentration varied significantly among specific sites within the MFSS collecting chamber (range, 0.8 +/- 0.5 x 10(4) to 575.0 +/- 56.3 x 10(4) cells/mL; mean +/- SEM). In Experiment 2, when porcine IVM oocytes were placed at three locations in the MFSS exit chamber (where only motile spermatozoa accumulated) and subsequently cultured in caffeine-free mM199 for 8 h, sperm penetration rate was not significantly different among places (86.1 +/- 10.5 to 100%), but the monospermic penetration rate was lower (P < 0.05) in oocytes 3.5 mm from the exit position (12.5 +/- 4.8%) than those at 7.5 mm (53.1 +/- 6.0%) or further (41.9 +/- 2.8%) from the exit. In Experiment 3, the normal fertilization index (ratio of monospermic oocytes to number of oocytes examined) 8 h after insemination was higher (P < 0.05) in the MFSS-IVF system (0.375 +/- 0.040) than both standard IVF and transient IVF (0.222 +/- 0.028 and 0.189 +/- 0.027, respectively, with co-culture for 8 h and for 5 min). Developmental competence of fertilized oocytes (blastocyst formation) was higher (P < 0.05) in the MFSS-IVF system (40.9 +/- 2.3%) than in either standard or transient IVF (22.6 +/- 1.4 and 33.7 +/- 3.5%). In conclusion, brief co-culture of porcine oocytes with spermatozoa gradually accumulated in the MFSS chamber improved the efficiency of producing monospermic fertilized embryos and blastocysts. Furthermore, efficiencies were significantly affected by oocyte location within the chamber.

摘要

本研究旨在使用微流控精子分选器(MFSS),该分选器设计用于使用层流(无离心)分离具有活力的人精子,用于猪 IVF。将猪精子以 1 x 10(8)个细胞/mL 的浓度用含有 20%精液的稀释液稀释,并在改良的 TCM-199(mM199,含 5 mM 咖啡因)中流动,将有活力的精子引入出口室进行 IVF。在实验 1 中,在流动 5 分钟后,MFSS 收集室特定部位的精子浓度差异显著(范围,0.8 +/- 0.5 x 10(4) 至 575.0 +/- 56.3 x 10(4) 个细胞/mL;平均值 +/- SEM)。在实验 2 中,当猪 IVM 卵母细胞放置在 MFSS 出口室的三个位置(只有活力精子聚集的位置),随后在无咖啡因的 mM199 中培养 8 小时时,不同位置的精子穿透率没有显著差异(86.1 +/- 10.5 至 100%),但离出口位置 3.5 毫米处的卵母细胞的单精子穿透率较低(P < 0.05)(12.5 +/- 4.8%),而离出口位置 7.5 毫米(53.1 +/- 6.0%)或更远(41.9 +/- 2.8%)的卵母细胞穿透率较低。在实验 3 中,在 MFSS-IVF 系统中,受精后 8 小时的正常受精指数(单精子卵母细胞与检查卵母细胞数的比值)(0.375 +/- 0.040)高于标准 IVF(0.222 +/- 0.028)和瞬时 IVF(0.189 +/- 0.027)(分别在 8 小时和 5 分钟的共培养后)。受精卵母细胞的发育能力(囊胚形成)在 MFSS-IVF 系统中(40.9 +/- 2.3%)高于标准 IVF(22.6 +/- 1.4%)和瞬时 IVF(33.7 +/- 3.5%)。总之,将猪卵母细胞与在 MFSS 室中逐渐积累的精子短暂共培养,提高了产生单精子受精胚胎和囊胚的效率。此外,效率显著受到卵母细胞在室中的位置的影响。

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