Maĭtesian E S, Kudriavtseva M V, Kudriavtsev E N
Tsitologiia. 1983 May;25(5):546-51.
Using a combined cytochemical method that allows to determine glycogen, DNA and 3H-thymidine label in the same cell, glycogen amounts were measured both in 3H-TdR-marked and non-marked hepatocytes of the regenerating 3H-thymidine. During mitosis, the glycogen amount is reduced if compared with that in cells being in presynthetic phase. It is proposed that the decrease in glycogen content in the regenerating liver may partly depend on energetic expenses of cells that started DNA synthesis and mitotic division. The phenotypic expression of genes responsible for glycogen synthesis and splitting in di-, tetra- and octoploid hepatocytes of the regenerating liver liver was proportional to the corresponding values.
使用一种能够在同一细胞中测定糖原、DNA和3H-胸腺嘧啶核苷标记的联合细胞化学方法,在再生的3H-胸腺嘧啶核苷标记和未标记的肝细胞中测量糖原含量。在有丝分裂期间,与处于合成前期的细胞相比,糖原含量降低。有人提出,再生肝脏中糖原含量的降低可能部分取决于开始DNA合成和有丝分裂的细胞的能量消耗。再生肝脏的二倍体、四倍体和八倍体肝细胞中负责糖原合成和分解的基因的表型表达与相应值成比例。