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早期牛胚胎对纤溶酶原的激活作用。

Activation of plasminogen by the early bovine embryo.

作者信息

Menino A R, Williams J S

出版信息

Biol Reprod. 1987 Jun;36(5):1289-95. doi: 10.1095/biolreprod36.5.1289.

DOI:10.1095/biolreprod36.5.1289
PMID:2956997
Abstract

Activation of the plasma zymogen plasminogen to the enzyme plasmin by the early bovine embryo was evaluated. Sixteen-cell embryos to early morulae were collected at death from handmated synchronized and superovulated crossbred beef cows. Embryos were cultured in Ham's F-12 medium supplemented with 15 mg/ml bovine serum albumin containing 0, 15, 30, 60 or 120 micrograms/ml plasminogen in a humidified atmosphere of 5% CO2 in air at 37 degrees C. Cultures were observed every day, and stage of development was recorded. Medium was collected at 24-h intervals, starting at initiation and continuing through 288 h of culture. Plasminogen activator and plasmin levels in the culture media were determined, using a caseinolytic assay. The percentages of embryos developing to the initiating hatching blastocyst, hatched blastocyst, attached blastocyst, and attached blastocyst with trophoblastic outgrowth stages were not significantly different between the five levels of plasminogen. Initiation and completion of hatching, however, accelerated as plasminogen concentration increased in the culture media. Plasminogen activator production, expressed as milliunits X ml-1 X h-1 X viable embryo-1, was low for the first 48 h of culture, increased between 48-120 h, and tended to plateau thereafter. Plasminogen activation, measured indirectly as the plasmin concentration in a microdrop of medium and expressed as microgram plasmin X ml-1 X h-1 X viable embryo-1, followed plasminogen activator production, and was consistently low for the first 48-72 h of culture. Embryonic activation of plasminogen increased sharply thereafter, and also plateaued after 120 h.

摘要

对早期牛胚胎将血浆酶原纤溶酶原激活为酶纤溶酶的情况进行了评估。从经人工授精同步化且超排的杂交肉牛母牛处收集死亡时处于16细胞胚胎至早期桑葚胚阶段的胚胎。胚胎在补充有15mg/ml牛血清白蛋白的Ham's F - 12培养基中培养,该培养基含有0、15、30、60或120μg/ml纤溶酶原,在37℃、含5%二氧化碳的空气的湿润环境中培养。每天观察培养情况,并记录发育阶段。从培养开始每隔24小时收集培养基,持续至培养288小时。使用酪蛋白溶解测定法测定培养基中纤溶酶原激活剂和纤溶酶水平。在五个纤溶酶原水平之间,发育至开始孵化囊胚、孵化囊胚、附着囊胚以及带有滋养层生长阶段的附着囊胚的胚胎百分比无显著差异。然而,随着培养基中纤溶酶原浓度增加,孵化的开始和完成加速。以毫单位×ml-1×h-1×存活胚胎-1表示的纤溶酶原激活剂产量在培养的前48小时较低,在48 - 120小时之间增加,此后趋于平稳。纤溶酶原激活以培养基微滴中的纤溶酶浓度间接测量,并以微克纤溶酶×ml-1×h-1×存活胚胎-1表示,其变化趋势与纤溶酶原激活剂产量一致,在培养的前48 - 72小时一直较低。此后,胚胎对纤溶酶原的激活急剧增加,并在120小时后也趋于平稳。

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