Campbell W J, Kelly D, Rizzino A
Eppley Institute for Cancer Research and Allied Diseases, University of Nebraska Medical Center, Omaha 68198.
In Vitro Cell Dev Biol. 1990 Dec;26(12):1181-5. doi: 10.1007/BF02623696.
Utilizing the technique of reverse transcription-polymerase chain reaction (RT-PCR), we have examined the expression of transforming growth factor-beta 3 (TGF-beta 3) by embryonal carcinoma (EC) cells, EC-derived differentiated cells and early mammalian embryos. Using a TGF-beta bioassay, we determined that PYS-2 cells express considerable TGF-beta activity that cannot be completely neutralized by antibodies specific for TGF-beta 1 and TGF-beta 2. We also have determined that PYS-2 cells, as well as F9 EC cells and their differentiated cells, express transcripts for TGF-beta 3. In addition, we have determined that blastocysts, cultured for three days in serum-containing medium, express TGF-beta 3 transcripts. Thus, our data suggest that expression of TGF-beta 3 is initiated during early stages of mammalian development.
利用逆转录-聚合酶链反应(RT-PCR)技术,我们检测了胚胎癌细胞(EC)、EC来源的分化细胞以及早期哺乳动物胚胎中转化生长因子β3(TGF-β3)的表达。通过TGF-β生物测定法,我们确定PYS-2细胞表达相当量的TGF-β活性,而该活性不能被TGF-β1和TGF-β2的特异性抗体完全中和。我们还确定PYS-2细胞以及F9 EC细胞及其分化细胞表达TGF-β3的转录本。此外,我们确定在含血清培养基中培养三天的囊胚表达TGF-β3转录本。因此,我们的数据表明TGF-β3的表达在哺乳动物发育的早期阶段就已开始。