Silaeva S A, Danilova N I
Vopr Med Khim. 1979 Jul-Aug;25(4):415-9.
Isoenzyme composition of thymidine kinase was studied in submitochondrial fractions of liver tissue with various proliferative activity (intact, regenerating livers and Zhaidel ascites hepatoma) using polyacrylamide gel disc electrophoresis. Three zones, corresponding to proteins with Rf 0.1-0.2 (I), Rf 0.5-0.55 (II) and Rf 0.85-0.87 (III) and exhibiting thymidine kinase activity, were found in fractions of cytoplasmic and mitochondrial matrix proteins from resting and proliferating rat liver tissues. In fractions of outer and inner mitochondrial membranes three zones of the enzymatic activity were also observed but two of them did not coincide in the Rf value with the thymidine kinase isoenzymes from cytoplasmic fraction and mitochondrial matrix: I Rf 0.1-0.16, II Rf 0.35-0.4 and III Rf 0.62-0.68. Redistribution of the enzymatic activity between thymidine kinase isozymes occurred in conversion of liver tissue from the resting state to increased proliferation. In these cases slowly migrating enzymatic fraction (Rf 0.1-0.2) was activated in mitochondrial matrix and membranes; formation of TMP, catalyzed by isozymes with fast mobility (Rf 0.5-0.55 in matrix and Rf 0.62-0.68 in membrane fractions of mitochondria), which are typical for intact liver tissue, was decreased, respectively.
利用聚丙烯酰胺凝胶圆盘电泳法,对具有不同增殖活性(正常肝脏、再生肝脏和吉田腹水肝癌)的肝组织亚线粒体组分中的胸苷激酶同工酶组成进行了研究。在静止和增殖大鼠肝组织的细胞质和线粒体基质蛋白组分中,发现了三个具有胸苷激酶活性的区域,其相对迁移率(Rf)分别为0.1 - 0.2(I区)、0.5 - 0.55(II区)和0.85 - 0.87(III区)。在线粒体外膜和内膜组分中也观察到了三个酶活性区域,但其中两个区域的Rf值与细胞质组分和线粒体基质中的胸苷激酶同工酶不一致:I区Rf为0.1 - 0.16,II区Rf为0.35 - 0.4,III区Rf为0.62 - 0.68。在肝组织从静止状态转变为增殖增强的过程中,胸苷激酶同工酶之间的酶活性发生了重新分布。在这些情况下,迁移较慢的酶组分(Rf 0.1 - 0.2)在线粒体基质和膜中被激活;而由迁移较快的同工酶(线粒体基质中Rf为0.5 - 0.55,线粒体膜组分中Rf为0.62 - 0.68)催化生成胸苷一磷酸(TMP)的过程分别减少,这些较快迁移的同工酶是正常肝脏组织所特有的。