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The ErbB signaling network in embryogenesis and oncogenesis: signal diversification through combinatorial ligand-receptor interactions.胚胎发生和肿瘤发生中的表皮生长因子受体(ErbB)信号网络:通过组合配体-受体相互作用实现信号多样化
FEBS Lett. 1997 Jun 23;410(1):83-6. doi: 10.1016/s0014-5793(97)00412-2.
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Expression of transforming growth factor alpha (TGF-alpha) gene in mouse embryonic development.转化生长因子α(TGF-α)基因在小鼠胚胎发育中的表达
J Assist Reprod Genet. 1997 May;14(5):262-9. doi: 10.1007/BF02765827.
5
Matrix metalloproteinase expression during mouse peri-implantation development.小鼠着床前期发育过程中基质金属蛋白酶的表达
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6
MT-MMP, the cell surface activator of proMMP-2 (pro-gelatinase A), is expressed with its substrate in mouse tissue during embryogenesis.MT - 基质金属蛋白酶(proMMP - 2,即前明胶酶A的细胞表面激活剂)在胚胎发育过程中与其底物一同在小鼠组织中表达。
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Effects of epidermal growth factor and transforming growth factor alpha on the mouse trophoblast outgrowth in vitro.表皮生长因子和转化生长因子α对体外培养的小鼠滋养层细胞生长的影响。
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8
Matrix metalloproteinases: a review.基质金属蛋白酶:综述
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Human cytotrophoblast invasion is up-regulated by epidermal growth factor: evidence that paracrine factors modify this process.表皮生长因子上调人细胞滋养层细胞的侵袭:旁分泌因子调节此过程的证据。
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转化生长因子-α对小鼠囊胚中基质金属蛋白酶-2、基质金属蛋白酶-9及表皮生长因子受体基因表达的影响

Influence of transforming growth factor-alpha on expression of matrix metalloproteinase-2, matrix metalloproteinase-9, and epidermal growth factor receptor gene in the mouse blastocysts.

作者信息

Kim Jeong Hee, Hong Seok Ho, Nah Hee Young, Lee Ji Yun, Chae Hee Dong, Kim Chung Hoon, Kang Byung Moon, Bae In Ha

机构信息

Department of Obstetrics and Gynecology, College of Medicine, Asan Medical Center, University of Ulsan, Seoul, South Korea.

出版信息

J Assist Reprod Genet. 2002 May;19(5):232-9. doi: 10.1023/a:1015310919415.

DOI:10.1023/a:1015310919415
PMID:12099554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3468233/
Abstract

PURPOSE

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。