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Enzymatic activity of mouse group X-sPLA2 improves in vitro production of preimplantation bovine embryos

机译:小鼠X-SPLA2的酶活性改善了牛胚的体外产生

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Assisted reproductive technologies (ART) are widely used for both humans and domestic animals. In bovine species, in vitro embryo production is increasingly used and significant efforts are being made to optimize media and culture conditions. Phospholipase A2 (PLA2) are lipolytic enzymes that hydrolyze glycerophospholipids to produce free fatty acids and lysophospholipids that have been found to be critical for many biological processes. Mouse group X secreted PLA(2) (mGX) is abundant in the male reproductive tract and its use during sperm capacitation has been shown to improve in vitro production of viable embryos in a mouse model. Here, we examined its effect in the bovine species, testing the impact of mGX on the three steps involved in vitro production of preimplantation embryos: oocyte maturation, fertilization and preimplantation development. We found that incubating cumulus oocyte complexes (COC) or gametes with mGX resulted in increased blastocyst hatching and blastocyst production, respectively. The increases of embryo production induced by the phospholipase mGX were not observed for the catalytically inactive mutant H48Q-mGX, suggesting that these effects require the enzymatic activity of mGX. We also tested bG1B, a bovine homolog of mGX. bGIB failed to improve blastocyst production, underlining the high specificity of mGX. In conclusion, the results presented show that the effects of mGX are not restricted to the mouse model and that it is potent in the bovine species as well. This result strengthens the potential of mGX as a "pro-fertility drug" for mammalian reproduction. (C) 2019 Elsevier Inc. All rights reserved.
机译:辅助生殖技术(ART)广泛用于人类和家畜。在牛种类中,越来越多地使用体外胚胎生产,并且正在大量努力优化培养基和培养条件。磷脂酶A2(PLA2)是脂解酶,其水解甘油磷脂以产生对许多生物过程至关重要的游离脂肪酸和溶血磷脂。小鼠组X分泌PLA(2)(MGX)在雄性生殖道中丰富,并且已经显示出在小鼠模型中改善活性胚胎的体外生产。在这里,我们在牛类中检查了它的效果,测试MGX对涉及预溶剂胚胎的三个步骤的影响:卵母细胞成熟,施肥和预热发育。我们发现孵育浓度卵母细胞配合物(COC)或用MGX的配子分别导致囊胚层孵化和胚泡产生增加。对于催化活性突变体H48Q-MGX未观察到磷脂酶MGX诱导的胚胎产生的增加,表明这些效应需要MGX的酶活性。我们还测试了BG1B,是MGX的牛同源物。 BGIB未能改善胚泡产生,强调MGX的高特异性。总之,提出的结果表明,MGX的影响不限于小鼠模型,也不限于牛种类。这一结果加强了MGX作为哺乳动物繁殖的“肥力药物”的潜力。 (c)2019 Elsevier Inc.保留所有权利。

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