Thomas T, Dziadek M
Centre for Early Human Development, Monash Medical Centre, Clayton, Victoria, Australia.
Biol Reprod. 1993 Dec;49(6):1251-9. doi: 10.1095/biolreprod49.6.1251.
The expression patterns of laminin A, B1, B2, and nidogen genes were identified by in situ hybridization in postimplantation mouse extraembryonic tissues and maternal decidua during the period when the chorioallantoic placenta is established. Laminin and nidogen genes were not coordinately expressed either in the decidua or in trophoblast cells, indicating that these genes are regulated independently in these cell types during the establishment of the placenta. Laminin A mRNA was absent from the decidua except in the outer layer of cells adjacent to the myometrium and in the central decidual zone adjacent to the remnant of the uterine epithelium on Day 9. At this stage laminin B1, B2, and nidogen genes were strongly expressed in these cells and also in other regions of the decidua. Laminin B1 mRNA was present at higher levels in the decidua capsularis than in the decidua basalis, while nidogen mRNA showed highest expression in the decidua basalis. Laminin B2 mRNA was produced uniformly throughout the decidua at very high levels, suggesting that laminin B2 chains may be an important component of the decidual matrix. By Day 11, the nidogen gene was expressed only in endothelial cells lining the maternal blood spaces within the decidua. Laminin B1 and nidogen mRNAs were found at high levels within trophoblast giant cells at all stages, while laminin A mRNA was detected in trophoblast giant cells at later stages and laminin B2 mRNA was not produced in high levels by these cells. The patterns of gene expression show a very high degree of regional specialization, suggesting that the extracellular matrices in different regions of the decidua and extraembryonic membranes are likely to be composed of quite different ratios of laminin and nidogen polypeptides.(ABSTRACT TRUNCATED AT 250 WORDS)
在绒毛膜尿囊胎盘形成期,通过原位杂交技术鉴定了层粘连蛋白A、B1、B2和巢蛋白基因在植入后小鼠胚胎外组织和母体蜕膜中的表达模式。层粘连蛋白和巢蛋白基因在蜕膜或滋养层细胞中并非协同表达,这表明在胎盘形成过程中,这些基因在这些细胞类型中是独立调控的。在第9天,除了与子宫肌层相邻的外层细胞以及与子宫上皮残余相邻的中央蜕膜区外,蜕膜中不存在层粘连蛋白A mRNA。在此阶段,层粘连蛋白B1、B2和巢蛋白基因在这些细胞以及蜕膜的其他区域强烈表达。层粘连蛋白B1 mRNA在包蜕膜中的水平高于底蜕膜,而巢蛋白mRNA在底蜕膜中表达最高。层粘连蛋白B2 mRNA在整个蜕膜中均以非常高的水平均匀产生,这表明层粘连蛋白B2链可能是蜕膜基质的重要组成部分。到第11天,巢蛋白基因仅在蜕膜内母体血窦内衬的内皮细胞中表达。在所有阶段,滋养层巨细胞中均发现高水平的层粘连蛋白B1和巢蛋白mRNA,而在后期滋养层巨细胞中检测到层粘连蛋白A mRNA,这些细胞不产生高水平的层粘连蛋白B2 mRNA。基因表达模式显示出高度的区域特异性,这表明蜕膜和胚胎外膜不同区域的细胞外基质可能由比例差异很大的层粘连蛋白和巢蛋白多肽组成。(摘要截断于250字)