Mohammadi Roushandeh Amaneh, Haji Hosseinlou Hassan, Niknafs Behrouz, Halabian Raheleh, Mehdipour Ahmad, Habibi Roudkenar Mehryar
Dept. of Anatomical Sciences, Medicine Faculty, Medical University of Tabriz, Tabriz, Iran.
Research Center, Iranian Blood Transfusion Organization (IBTO), Tehran, Iran.
Iran Biomed J. 2010 Jul;14(3):103-7.
Leukemia inhibitory factor (LIF) is a 45-56 kDa glycoprotein that has an important role in proliferation and embryo implantation. Its effect on oocyte maturation and how to exert the function remained to be elucidated.
Immature mice superovulated with human menopausal gonadotropin and germinal vesicle (GV) oocytes were obtained from ovary 48 hours after. GV oocytes were cultured in tissue culture medium 199 with 0, 100, 500 and 1,000 U/ml LIF. Cumulus expansion and in vitro maturation (IVM) rate were assessed after culture. For reverse transcriptase PCR, total RNA from GV and metaphase II (MII) oocytes were extracted by Trizol reagent. The quantity and quality of RNA were determined by spectrophotometry and electrophoresis, respectively. Reverse transcription was performed by Super Script III reverse transcriptase with 1 µg of total RNA followed by DNase I treatment and heat inactivation. Expression of gp130 was determined by RT-PCR.
Our results showed that cumulus expansion was improved with 1,000 U/ml in culture medium compared to others. GV breakdown and MII rate in groups with LIF were higher than control group and were dose-dependent. In 1,000 U/ml, LIF rate of MII was significantly higher than control group (P less than 0.05). Our results also showed that gp130 is expressed neither in GV nor in MII oocytes during IVM of mouse oocytes.
gp130 is expressed in human oocyte but not in mouse. Our results suggest that in mouse, LIF could affect the oocyte via another receptor or via cumulus cells; however, further studies are warranted.
白血病抑制因子(LIF)是一种45 - 56 kDa的糖蛋白,在细胞增殖和胚胎着床中起重要作用。其对卵母细胞成熟的影响以及作用机制尚待阐明。
用人绝经期促性腺激素对未成熟小鼠进行超排卵,48小时后从卵巢获取生发泡(GV)期卵母细胞。将GV期卵母细胞在含有0、100、500和1000 U/ml LIF的199组织培养液中培养。培养后评估卵丘扩展和体外成熟(IVM)率。对于逆转录聚合酶链反应(RT-PCR),用Trizol试剂从GV期和中期II(MII)期卵母细胞中提取总RNA。分别通过分光光度法和电泳测定RNA的数量和质量。用1 μg总RNA通过Super Script III逆转录酶进行逆转录,随后进行DNA酶I处理和热灭活。通过RT-PCR测定gp130的表达。
我们的结果表明,与其他组相比,培养液中1000 U/ml的LIF可改善卵丘扩展。添加LIF组的GV期卵母细胞破裂和MII期比率高于对照组,且呈剂量依赖性。在1000 U/ml时,MII期比率显著高于对照组(P小于0.05)。我们的结果还表明,在小鼠卵母细胞IVM过程中,GV期和MII期卵母细胞均未表达gp130。
gp130在人卵母细胞中表达,但在小鼠中不表达。我们的结果表明,在小鼠中,LIF可能通过另一种受体或通过卵丘细胞影响卵母细胞;然而,仍需进一步研究。