Gelly J L, Richoux J P, Grignon G, Bouhnik J, Baussant T, Alhenc-Gelas F, Corvol P
Laboratoire d'Histologie-Embryologie, Faculté de Médecine, Vandoeuvre-les-Nancy, France.
Histochemistry. 1991;96(1):7-12. doi: 10.1007/BF00266754.
Rat albumin, transferrin, angiotensinogen, T kininogen (TKg) and high molecular weight kininogen (HKg) gene expression was examined immunocytochemically in embryonic and fetal livers. All these plasmatic proteins, angiotensinogen excepted, are detected as early as day 11 of gestation in intestine epithelial cells and embryonic hepatocytes. Angiotensinogen becomes expressible only at day 13 of gestation. During the early fetal period, the protein immunostaining increases strikingly in parallel with the hepatocyte differentiation. Albumin and transferrin are highly expressed comparatively to kininogens and angiotensinogen. For the first time, specific HKg is demonstrated in the rat liver.
采用免疫细胞化学方法检测了大鼠胚胎和胎儿肝脏中白蛋白、转铁蛋白、血管紧张素原、T 激肽原(TKg)和高分子量激肽原(HKg)的基因表达。除血管紧张素原外,所有这些血浆蛋白早在妊娠第 11 天就在肠上皮细胞和胚胎肝细胞中被检测到。血管紧张素原仅在妊娠第 13 天才开始表达。在胎儿早期,蛋白质免疫染色随着肝细胞分化显著增加。与激肽原和血管紧张素原相比,白蛋白和转铁蛋白高度表达。首次在大鼠肝脏中证实了特异性 HKg 的存在。