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成熟培养液中的氨基酸以及受精时卵丘细胞的存在,可促进体外成熟并受精的猪卵母细胞雄原核的形成。

Amino acids in maturation medium and presence of cumulus cells at fertilization promote male pronuclear formation in porcine oocytes matured and penetrated in vitro.

作者信息

Ka H H, Sawai K, Wang W H, Im K S, Niwa K

机构信息

Division of Animal Science and Technology, Faculty of Agriculture, Okayama University, Japan.

出版信息

Biol Reprod. 1997 Dec;57(6):1478-83. doi: 10.1095/biolreprod57.6.1478.

Abstract

The present study was conducted to examine the ability of porcine oocytes to achieve male pronuclear (MPN) formation when they are matured and penetrated in vitro under various culture conditions. When cumulus-enclosed oocytes were cultured for 24-48 h in modified Whitten's medium (pH 7.4) supplemented with 10% porcine follicular fluid, 10 IU eCG/ml, and 10 IU hCG/ml (designated mWM-FG), nuclear maturation of oocytes reaching metaphase II was completed by 36 h after the start of culture. However, there were no differences in the proportions (94-95%) of oocytes penetrated in vitro by cryopreserved ejaculated spermatozoa or in the rates (35-45%) of MPN formation between oocytes cultured for 36 and 48 h. When cumulus-enclosed oocytes were cultured for 36 h in mWM-FG supplemented with 2% (v:v) minimal essential medium (MEM) essential amino acids (EAA) with the addition of 0.1 mM glutamine and/or 1% (v:v) MEM nonessential amino acids (NEAA) and inseminated in vitro, 93-97% of oocytes were penetrated regardless of the presence of amino acids during maturation, but the rates of MPN formation were higher in the presence (79-84%) than in the absence (51%) of any amino acids. The addition of EAA+NEAA and/or 0.57 mM cysteine to mWM-FG also did not affect sperm penetration in vitro, while it promoted MPN formation (76-83%) in penetrated oocytes as compared with those matured in the absence of amino acids and cysteine (53%). When oocytes were freed from cumulus cells after culture in mWM-FG, sperm penetration rates were not different between cumulus-enclosed (100%) and cumulus-free (92%) oocytes, but the rate of MPN formation was higher in cumulus-enclosed (53%) than in cumulus-free (28%) oocytes. When EAA+NEAA+cysteine was added to mWM-FG, MPN formation was not improved in cumulus-free oocytes but was much improved (78%) in cumulus-enclosed oocytes. These results indicate that MPN formation in porcine oocytes is promoted by the addition of amino acids and/or cysteine in simple maturation medium and by the presence of cumulus cells at fertilization in vitro.

摘要

本研究旨在检测猪卵母细胞在不同培养条件下体外成熟和受精时形成雄原核(MPN)的能力。当卵丘细胞包裹的卵母细胞在添加了10%猪卵泡液、10 IU促性腺激素(eCG)/ml和10 IU人绒毛膜促性腺激素(hCG)/ml的改良惠滕氏培养基(pH 7.4)(称为mWM-FG)中培养24 - 48小时时,培养开始后36小时,达到减数分裂中期II的卵母细胞核成熟完成。然而,冷冻保存的射出精子体外穿透卵母细胞的比例(94 - 95%)以及培养36小时和48小时的卵母细胞中MPN形成率(35 - 45%)之间没有差异。当卵丘细胞包裹的卵母细胞在添加了2%(v:v)基本培养基(MEM)必需氨基酸(EAA)并添加0.1 mM谷氨酰胺和/或1%(v:v)MEM非必需氨基酸(NEAA)的mWM-FG中培养36小时并进行体外受精时,无论成熟过程中是否存在氨基酸,93 - 97%的卵母细胞都能被穿透,但存在任何氨基酸时MPN形成率(79 - 84%)高于不存在时(51%)。向mWM-FG中添加EAA + NEAA和/或0.57 mM半胱氨酸也不影响精子体外穿透,而与在无氨基酸和半胱氨酸条件下成熟的卵母细胞相比,其促进了穿透卵母细胞中MPN的形成(76 - 83%)(53%)。当卵母细胞在mWM-FG中培养后去除卵丘细胞时,卵丘细胞包裹的卵母细胞(100%)和去卵丘细胞的卵母细胞(92%)的精子穿透率没有差异,但卵丘细胞包裹的卵母细胞(53%)的MPN形成率高于去卵丘细胞的卵母细胞(28%)。当向mWM-FG中添加EAA + NEAA + 半胱氨酸时,去卵丘细胞的卵母细胞中MPN形成没有改善,但在卵丘细胞包裹的卵母细胞中得到显著改善(78%)。这些结果表明,在简单的成熟培养基中添加氨基酸和/或半胱氨酸以及体外受精时卵丘细胞的存在可促进猪卵母细胞中MPN的形成。

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