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糖蛋白 130 促进人囊胚体外发育。

Glycoprotein 130 promotes human blastocyst development in vitro.

机构信息

Department of Clinical Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Fertil Steril. 2013 May;99(6):1592-9. doi: 10.1016/j.fertnstert.2012.12.041. Epub 2013 Jan 30.

DOI:10.1016/j.fertnstert.2012.12.041
PMID:23375201
Abstract

OBJECTIVE

To investigate the efficacy of leukemia inhibitory factor (LIF) and/or glycoprotein 130 (gp130) on in vitro growth of human embryos.

DESIGN

Laboratory study.

SETTING

University hospital-based IVF clinic.

PATIENT(S): A total of 164 frozen embryos that survived thawing were cultured in media supplemented with LIF and/or gp130 or control media.

INTERVENTION(S): Morphological development was evaluated by light microscopy. Protein expression profiles of single blastocysts were evaluated using matrix-assisted laser desorption/ionization time of flight-based intact cell mass spectrometry.

MAIN OUTCOME MEASURE(S): Embryo development and protein content.

RESULT(S): Addition of gp130 to culture media improved blastocyst formation (73% vs. 43%). Addition of LIF to the culture media did not improve embryo development. Protein fingerprint spectra were obtained that revealed significant intensity changes for multiple molecular species including thymosin beta-10, thymosin beta-4, histone H2A, histone H2B, histone H4, ubiquitin, ubiquitin-T, and acyl-CoA binding protein.

CONCLUSION(S): Glycoprotein 130, but not LIF, seems to be beneficial for preimplantation embryo development, implicating a physiological role in regulating preimplantation development in humans and thus ought to be included in culture media designed for embryo culture to the blastocyst stage. Furthermore, these findings highlight the great potential of matrix-assisted laser desorption/ionization time of flight mass spectrometry and intact cell mass spectrometry as a versatile tool in reproductive medicine research.

摘要

目的

研究白血病抑制因子(LIF)和/或糖蛋白 130(gp130)对人胚胎体外生长的疗效。

设计

实验室研究。

地点

大学医院的 IVF 诊所。

患者

共 164 个冷冻胚胎解冻后存活,在添加 LIF 和/或 gp130 的培养基或对照培养基中培养。

干预

通过相差显微镜评估形态发育。使用基质辅助激光解吸/电离飞行时间基于完整细胞质量谱法评估单个囊胚的蛋白质表达谱。

主要观察指标

胚胎发育和蛋白质含量。

结果

添加 gp130 到培养基中提高了囊胚形成率(73%对 43%)。添加 LIF 到培养基中并不能改善胚胎发育。获得了蛋白质指纹图谱,揭示了多个分子种类的显著强度变化,包括胸腺素β-10、胸腺素β-4、组蛋白 H2A、组蛋白 H2B、组蛋白 H4、泛素、泛素-T 和酰基辅酶 A 结合蛋白。

结论

糖蛋白 130,而不是 LIF,似乎对植入前胚胎发育有益,暗示其在调节人类植入前发育中具有生理作用,因此应该包含在设计用于胚胎培养至囊胚阶段的培养基中。此外,这些发现突出了基质辅助激光解吸/电离飞行时间质谱和完整细胞质谱作为生殖医学研究中通用工具的巨大潜力。

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