Slager H G, Lawson K A, van den Eijnden-van Raaij A J, de Laat S W, Mummery C L
Hubrecht Laboratory, The Netherlands Institute for Developmental Biology, Utrecht.
Dev Biol. 1991 Jun;145(2):205-18. doi: 10.1016/0012-1606(91)90120-r.
The localization of transforming growth factor type beta 2 (TGF-beta 2) has been followed during preimplantation and early postimplantation murine development using an anti-peptide antibody that specifically recognizes TGF-beta 2. The staining pattern showed that TGF-beta 2 is expressed from the four-cell stage onward and is differentially regulated as cells diverge to various lineages. High levels of staining were found in the trophectoderm of the blastocyst but no staining was observed in the inner cell mass. During postimplantation development the primitive and embryonic ectoderm also lacked detectable staining while visceral endoderm stained well. Parietal endoderm cells also showed positive staining reaction although to a lesser extent than visceral endoderm cells. These findings were confirmed in model systems of the embryo, namely, embryonal carcinoma and embryonic stem cells differentiated to to cells with either visceral or parietal endoderm characteristics. The possible regulatory role of this factor in early embryogenesis is discussed.
利用一种能特异性识别转化生长因子β2(TGF-β2)的抗肽抗体,对小鼠植入前和植入后早期发育过程中TGF-β2的定位进行了追踪研究。染色模式显示,TGF-β2从四细胞阶段开始表达,并且随着细胞分化为不同谱系而受到差异调节。在囊胚的滋养外胚层中发现了高水平的染色,但在内细胞团中未观察到染色。在植入后发育过程中,原始外胚层和胚胎外胚层也缺乏可检测到的染色,而脏内胚层染色良好。壁内胚层细胞也显示出阳性染色反应,尽管程度低于脏内胚层细胞。这些发现在胚胎的模型系统中得到了证实,即胚胎癌细胞和分化为具有脏内胚层或壁内胚层特征细胞的胚胎干细胞。本文讨论了该因子在早期胚胎发生中可能的调节作用。