Khramtsova S N, Alekhina R P, Potapova G I, Shapot V S
Biull Eksp Biol Med. 1985 Nov;100(11):602-5.
The tightness of DNA-protein binding in the nuclei of mouse spleen T- and B-lymphocytes was assessed, using nucleoprotein celite chromatography, and changes in the number of T- and B-suppressors in the course of o-AAT-induced chemical hepatocarcinogenesis were studied. Attenuation of DNA-protein bonds in T-lymphocytes at the early stages (up to 3 months) was observed, and by the time of hepatoma formation (8 months) about 50% of T-lymphocyte DNA was loosely bound to proteins, which is a typical feature of quiescent cells. In B-lymphocytes attenuation of DNA-protein interaction was only observed by the 8th month of carcinogenesis. By the time of hepatoma formation the number of T-suppressors in mouse spleen increased 2.8-fold, while the number of B-suppressors in lymph nodes remained unchanged.
利用核蛋白硅藻土色谱法评估了小鼠脾脏T淋巴细胞和B淋巴细胞细胞核中DNA与蛋白质结合的紧密程度,并研究了在邻氨基苯甲酰-L-酪氨酸(o-AAT)诱导的化学性肝癌发生过程中T抑制细胞和B抑制细胞数量的变化。在早期阶段(长达3个月)观察到T淋巴细胞中DNA与蛋白质结合键的减弱,到肝癌形成时(8个月),约50%的T淋巴细胞DNA与蛋白质松散结合,这是静止细胞的典型特征。在B淋巴细胞中,直到致癌作用的第8个月才观察到DNA与蛋白质相互作用的减弱。到肝癌形成时,小鼠脾脏中T抑制细胞的数量增加了2.8倍,而淋巴结中B抑制细胞的数量保持不变。