Beckman D A, Pugarelli J E, Jensen M, Koszalka T R, Brent R L, Lloyd J B
Department of Pediatrics, Thomas Jefferson University, Philadelphia, PA 19107.
Placenta. 1990 Mar-Apr;11(2):109-21. doi: 10.1016/s0143-4004(05)80173-0.
Rat conceptuses on the 10th day of gestation were cultured for 27 h in whole rat serum. An addition of either [3H]leucine or [3H]leucine-labelled rat serum proteins was made once during the culture period, and the acid-soluble and acid-insoluble radioactivities of embryo and visceral yolk sac measured at harvesting. The extent of radiolabel incorporation into embryonic and yolk-sac proteins increased linearly with the duration of exposure of the conceptus to the radiolabelled leucine or radiolabelled serum proteins, indicating roughly constant rates of incorporation, per unit mass of tissue, throughout the culture period. The incorporation rates, expressed as clearances, were 0.73 and 0.78 microliter/mg tissue protein/h for embryo and yolk sac, respectively, when the source was [3H]leucine; and 1.8 and 1.3 microliters/mg tissue protein/h, for embryo and yolk sac, respectively, when the source was [3H]leucine-labelled serum proteins. It is estimated, from the known leucine and protein concentrations in serum, that protein contributed over 99 per cent of the leucine supplied to the conceptus for its protein synthesis. In parallel experiments, measurements were made on cultures conducted in the presence of an antiserum against rat visceral yolk sac (100 micrograms/ml). Antiserum profoundly inhibited incorporation of radioactivity into embryo and yolk-sac proteins, when the source was 3H-labelled protein, a result consistent with the known ability of the antiserum to inhibit pinocytosis in the yolk sac. Antiserum also decreased incorporation from [3H]leucine in the yolk sac, suggesting that a proportion of the free leucine entering the yolk sac does so by pinocytosis. The failure of antiserum to affect incorporation of [3H]leucine into the embryo probably indicates that leucine can enter the embryo without the mediation of yolk-sac pinocytosis. The primacy of protein, as a source of amino acids for the organogenesis-stage embryo, is consistent with the serious effects, in terms of embryonic death and malformation, that result from the interruption of amino acid supply when either pinocytosis or lysosomal proteolysis in the yolk sac is inhibited.
将妊娠第10天的大鼠胚胎在全大鼠血清中培养27小时。在培养期间添加一次[3H]亮氨酸或[3H]亮氨酸标记的大鼠血清蛋白,收获时测定胚胎和内脏卵黄囊的酸溶性和酸不溶性放射性。放射性标记掺入胚胎和卵黄囊蛋白的程度随胚胎暴露于放射性标记亮氨酸或放射性标记血清蛋白的时间呈线性增加,表明在整个培养期间,每单位组织质量的掺入率大致恒定。当来源为[3H]亮氨酸时,胚胎和卵黄囊的掺入率(以清除率表示)分别为0.73和0.78微升/毫克组织蛋白/小时;当来源为[3H]亮氨酸标记的血清蛋白时,胚胎和卵黄囊的掺入率分别为1.8和1.3微升/毫克组织蛋白/小时。根据血清中已知的亮氨酸和蛋白质浓度估计,蛋白质为胚胎蛋白质合成提供的亮氨酸超过99%。在平行实验中,对在抗大鼠内脏卵黄囊抗血清(100微克/毫升)存在下进行的培养物进行了测量。当来源为3H标记的蛋白质时,抗血清显著抑制放射性掺入胚胎和卵黄囊蛋白,这一结果与抗血清抑制卵黄囊胞饮作用的已知能力一致。抗血清也降低了卵黄囊中[3H]亮氨酸的掺入,表明进入卵黄囊的一部分游离亮氨酸是通过胞饮作用进入的。抗血清未能影响[3H]亮氨酸掺入胚胎可能表明亮氨酸可以在没有卵黄囊胞饮作用介导的情况下进入胚胎。蛋白质作为器官发生期胚胎氨基酸来源的首要地位,与卵黄囊中胞饮作用或溶酶体蛋白水解作用受到抑制时氨基酸供应中断所导致的胚胎死亡和畸形等严重影响是一致的。