Ogura R, Kaneko N, Hidaka T
Arch Dermatol Res. 1986;278(5):382-5. doi: 10.1007/BF00418167.
DNA polymerase activity was determined in hyperkeratotic epidermis of the guinea pig by topical application of n.hexadecane. Epidermal cells were separated by Percoll gradient centrifugation. DNA polymerase alpha activity was higher in the basal cells, but polymerase beta activity was higher in granular cells than in cells from the other layers. The hyperkeratosis was accompanied by an increase in polymerase alpha activity in both the squamous and basal cells. However, polymerase beta activity decreased in the granular cells and was distributed almost uniformly across the epidermis. The distribution pattern of polymerase activities in the hyperkeratotic epidermis was not simply an enhancement of the pattern in normal epidermis.
通过局部涂抹正十六烷来测定豚鼠角化过度表皮中的DNA聚合酶活性。表皮细胞通过Percoll梯度离心法分离。DNA聚合酶α活性在基底细胞中较高,但聚合酶β活性在颗粒细胞中高于其他层的细胞。角化过度伴随着鳞状细胞和基底细胞中聚合酶α活性的增加。然而,颗粒细胞中的聚合酶β活性降低,且几乎均匀分布于整个表皮。角化过度表皮中聚合酶活性的分布模式并非简单地增强了正常表皮中的模式。