Kim Jeong Hee, Hong Seok Ho, Nah Hee Young, Lee Ji Yun, Chae Hee Dong, Kim Chung Hoon, Kang Byung Moon, Bae In Ha
Department of Obstetrics and Gynecology, College of Medicine, Asan Medical Center, University of Ulsan, Seoul, South Korea.
J Assist Reprod Genet. 2002 May;19(5):232-9. doi: 10.1023/a:1015310919415.
This study was carried out to investigate the influence of transforming growth factor-alpha (TGF-alpha) on the expression of mRNA for matrix metalloproteinase-2 (MMP-2), MMP-9, and epidermal growth factor receptor (EGFR) in mouse blastocysts and the effect on the production and activation of MMP-2 and MMP- 9 during blastocyst outgrowth.
Two-cell mouse embryos were cultured for 96 h in the presence or absence of various concentrations of TGF-alpha. Reverse transcription-polymerase chain reaction (RT-PCR) was used to examine the expression of mRNA for MMP-2, MMP-9, and EGFR in in vitro cultured blastocysts. To investigate the effect on the production and activation of MMP-2 and MMP-9 during blastocyst outgrowth, the conditioned medium collected after 3 and 5 days of embryo culture were assayed for MMP activity by gelatin zymography.
The relative mRNA levels of MMP-2 and MMP-9 in blastocysts treated with TGF-alpha were higher than that of the control in a concentration-dependent manner. The relative mRNA level of EGFR in blastocysts treated with TGF-alpha was higher than that of the control. In conditioned medium collected after 3 days of embryo culture, TGF-alpha induced the gelatinase activities of proMMP-9 in all groups and activated MMP-2 in the 10 and 100 ng/mL TGF-alpha treated groups. In conditioned medium collected after 5 days, TGF-alpha induced the gelatinase activities of proMMP-9 in all groups and activated MMP-9 in the TGF-alpha treated group. TGF-alpha also induced the gelatinase activities of activated MMP-2 in the 1 and 10 ng/mL TGF-alpha treated groups and the control.
These results suggest that the addition of TGF-alpha to in vitro culture medium is proper to create a favorable environment for preimplantation embryo development and implantation.
本研究旨在探讨转化生长因子-α(TGF-α)对小鼠囊胚中基质金属蛋白酶-2(MMP-2)、MMP-9和表皮生长因子受体(EGFR)mRNA表达的影响,以及对囊胚孵出过程中MMP-2和MMP-9产生和激活的作用。
将二细胞期小鼠胚胎在存在或不存在不同浓度TGF-α的情况下培养96小时。采用逆转录-聚合酶链反应(RT-PCR)检测体外培养囊胚中MMP-2、MMP-9和EGFR的mRNA表达。为了研究对囊胚孵出过程中MMP-2和MMP-9产生和激活的影响,通过明胶酶谱法检测胚胎培养3天和5天后收集的条件培养基中的MMP活性。
用TGF-α处理的囊胚中,MMP-2和MMP-9的相对mRNA水平高于对照组,呈浓度依赖性。用TGF-α处理的囊胚中EGFR的相对mRNA水平高于对照组。在胚胎培养3天后收集的条件培养基中,TGF-α在所有组中诱导了proMMP-9的明胶酶活性,并在10和100 ng/mL TGF-α处理组中激活了MMP-2。在培养5天后收集的条件培养基中,TGF-α在所有组中诱导了proMMP-9的明胶酶活性,并在TGF-α处理组中激活了MMP-9。TGF-α还在1和10 ng/mL TGF-α处理组及对照组中诱导了激活的MMP-2的明胶酶活性。
这些结果表明,在体外培养基中添加TGF-α有利于为着床前胚胎发育和着床创造良好环境。