Kistler A, Yoshizato K, Frieden E
Endocrinology. 1975 Oct;97(4):1036-42. doi: 10.1210/endo-97-4-1036.
The binding of L-triiodothyronine (T3) and L-thyroxine (T4) to cytoplasm and nuclei has been studied in isolated Rana catesbeiana tadpole liver cells. Nuclear binding for both thyroid hormones occurred more slowly at 4 C than at 25 C, but reached the same level as at 25 S. Scatchard analyses suggest high affinity, saturable binding sites for both hormones in the nuclear but not in the cytoplasmic fraction. Apparent equilibrium dissociation constants were 6.8 X 10(-10)M and 4.6 X 10(-10)M for T3 and T4, respectively. The maximum number of binding sites per nucleus for T3 was about 12,300 and for T4 about 2,300. Unlabeled T3 competed for the binding of [125I]T3 to nuclei more effectively than unlabeled T4. No difference in the competition of [125I]T4 binding with non-radioactive T3 or T4 was found. Chromatographic analysis of the bound nuclear radioactivity demonstrated no chemical modification for either hormone.
在分离的牛蛙蝌蚪肝细胞中,研究了L-三碘甲状腺原氨酸(T3)和L-甲状腺素(T4)与细胞质和细胞核的结合情况。两种甲状腺激素的核结合在4℃时比在25℃时发生得更慢,但最终达到与25℃时相同的水平。Scatchard分析表明,两种激素在细胞核部分存在高亲和力、可饱和的结合位点,而在细胞质部分则不存在。T3和T4的表观平衡解离常数分别为6.8×10⁻¹⁰M和4.6×10⁻¹⁰M。每个细胞核中T3的最大结合位点数约为12300个,T4约为2300个。未标记的T3比未标记的T4更有效地竞争[¹²⁵I]T3与细胞核的结合。未发现[¹²⁵I]T4与非放射性T3或T4竞争结合的差异。对结合的核放射性进行色谱分析表明,两种激素均未发生化学修饰。