Srivastava U S, Thakur M L, Majumdar P K, Bhatnagar G M, Supakar P C
J Nutr. 1987 Feb;117(2):242-6. doi: 10.1093/jn/117.2.242.
Synthesis of mRNA was studied in the spleen and thymus of rats that had been exposed to undernutrition early in life. To achieve this objective, lactating females were separated into two groups 1 wk after they gave birth to offspring. These control and experimental dams suckled 8-11 and 13-16 pups, respectively, for a period of 2 wk. The young of both groups were then killed, and their thymus and spleen were isolated. Polyadenylated RNA (poly A+ RNA) was fractionated by affinity chromatography on an oligo-dT-cellulose column. Poly A+ RNA content as well as the percentage of poly A+ RNA in relation to total RNA were both lower in the undernourished pups than in the controls. Analysis of the in vitro translation product primed by poly A+ RNA of the thymus and spleen revealed a rise in [35S]methionine incorporation in the undernourished offspring, the increase being greater in the thymus than in the spleen. Sodium dodecyl sulfate polyacrylamide-gel electrophoresis, autoradiography and densitometric autoradiographic tracings confirmed these findings and demonstrated that proteins were synthesized at a higher level in the spleen and thymus of the undernourished rats than in the controls. These results show that undernutrition early in life could modulate the metabolism of mRNA and, consequently, protein synthesis in the lymphoid organs of rats. Furthermore, the data suggest that cell-mediated immunity as well as humoral immunity are both deranged in protein energy undernutrition.
对生命早期遭受营养不良的大鼠的脾脏和胸腺中的mRNA合成进行了研究。为实现这一目标,在哺乳期雌性大鼠产仔1周后将其分为两组。这些对照组和实验组的母鼠分别哺育8 - 11只和13 - 16只幼崽,为期2周。然后将两组幼崽处死,并分离出它们的胸腺和脾脏。通过在寡聚dT - 纤维素柱上进行亲和层析对聚腺苷酸化RNA(poly A+ RNA)进行分级分离。营养不良幼崽的poly A+ RNA含量以及poly A+ RNA相对于总RNA的百分比均低于对照组。对胸腺和脾脏的poly A+ RNA引发的体外翻译产物的分析显示,营养不良后代中[35S]甲硫氨酸掺入量增加,胸腺中的增加幅度大于脾脏。十二烷基硫酸钠聚丙烯酰胺凝胶电泳、放射自显影和光密度放射自显影片证实了这些发现,并表明营养不良大鼠的脾脏和胸腺中蛋白质合成水平高于对照组。这些结果表明,生命早期的营养不良可调节mRNA的代谢,进而调节大鼠淋巴器官中的蛋白质合成。此外,数据表明在蛋白质能量营养不良中,细胞介导免疫和体液免疫均受到干扰。