Gordon A, Schwartz H, Gross J
Acta Endocrinol (Copenh). 1987 Jun;115(2):259-64. doi: 10.1530/acta.0.1150259.
T3 stimulated, in a dose dependent manner, the uptake of 2-deoxy-D-glucose (2-DOG) into cultured chick embryo carcass derived cells. A significant increase in sugar uptake was seen already at a T3 concentration of 1 pmol/l. The stimulation of 2-DOG uptake increased with time during the 6 h of exposure to T3. The hormone also stimulated, within 45 min, the incorporation of [3H]leucine and [3H]uridine into the trichloroacetic acid precipitable material of these cells. Actinomycin-D (100 micrograms/l) and cycloheximide (1 mg/l) each were capable of blocking the stimulatory effect of 10(-8) mol/l T3 on sugar uptake and on uridine and leucine incorporation. Thus, T3 in these cultured chick embryo cells stimulated sugar transport through processes dependent on neosynthesis of proteins. In this respect the effect of T3 is different from that seen in cultured chick embryo cardiomyocytes.
T3 以剂量依赖的方式刺激培养的鸡胚胴体来源细胞摄取 2-脱氧-D-葡萄糖(2-DOG)。在 T3 浓度为 1 pmol/l 时,糖摄取就已显著增加。在暴露于 T3 的 6 小时内,2-DOG 摄取的刺激作用随时间增加。该激素还在 45 分钟内刺激了 [3H]亮氨酸和 [3H]尿苷掺入这些细胞的三氯乙酸沉淀物质中。放线菌素-D(100 微克/升)和环己酰亚胺(1 毫克/升)均能够阻断 10(-8) 摩尔/升 T3 对糖摄取以及尿苷和亮氨酸掺入的刺激作用。因此,在这些培养的鸡胚细胞中,T3 通过依赖蛋白质新合成的过程刺激糖转运。在这方面,T3 的作用与在培养的鸡胚心肌细胞中观察到的不同。