Reiners J J, Rupp T
Department of Carcinogenesis, University of Texas M.D. Anderson Cancer Center, Smithville 78957.
J Invest Dermatol. 1989 Jul;93(1):132-5. doi: 10.1111/1523-1747.ep12277382.
The distributions of xanthine dehydrogenase (XD) and xanthine oxidase (XO) in subpopulations of murine keratinocytes differing in their stages of terminal differentiation were determined by enzymatic analyses. Keratinocytes were isolated from the skins of female SENCAR mice that had been treated 72 h earlier with either acetone or 12-O-tetradecanoylphorbol-13-acetate (TPA). The ratio of XO/(XD + XO) specific activities was used as an index of the XD to XO conversion. The XO/(XD + XO) ratios for basal cell, suprabasal cell, granular cell plus squamae, and horny sheet preparations isolated from acetone- or TPA-treated mice were 0.35, 0.35, 0.45, 0.75 and 0.28, 0.29, 0.58, and 1.0, respectively. Total XD + XO and XO specific activities in each subpopulation derived from TPA-treated mice were approximately twice the values measured in their control counterparts. Suspension culturing of basal cell keratinocytes in methylcellulose induced terminal differentiation and a conversion of XD to XO. The kinetics of keratin disulfide crosslinking and the XD to XO conversion were similar and preceded cornification. Collectively, these studies demonstrate that the conversion of XD to XO occurs primarily during the later stages of keratinocyte terminal differentiation. Furthermore, the increases in XO activity measured in epidermal homogenates after TPA treatment are due to TPA-dependent increases in 1) the relative proportions of keratinocytes undergoing differentiation, 2) tissue XD content, and 3) increased conversion of XD to XO.
通过酶学分析确定了黄嘌呤脱氢酶(XD)和黄嘌呤氧化酶(XO)在终末分化阶段不同的小鼠角质形成细胞亚群中的分布。从雌性SENCAR小鼠的皮肤中分离角质形成细胞,这些小鼠在72小时前用丙酮或12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)处理过。XO /(XD + XO)比活性被用作XD向XO转化的指标。从丙酮或TPA处理的小鼠中分离的基底细胞、基底上层细胞、颗粒细胞加鳞屑以及角质层制剂的XO /(XD + XO)比值分别为0.35、0.35、0.45、0.75和0.28、0.29、0.58及1.0。来自TPA处理小鼠的每个亚群中的总XD + XO和XO比活性大约是其对照对应物测量值的两倍。在甲基纤维素中悬浮培养基底细胞角质形成细胞可诱导终末分化以及XD向XO的转化。角蛋白二硫键交联和XD向XO转化的动力学相似且先于角质化。总体而言,这些研究表明XD向XO的转化主要发生在角质形成细胞终末分化的后期。此外,TPA处理后表皮匀浆中测量到的XO活性增加是由于TPA依赖性增加:1)经历分化的角质形成细胞的相对比例,2)组织XD含量,以及3)XD向XO的转化增加。