Stenn K S, Core N G, Halaban R
J Invest Dermatol. 1986 Dec;87(6):754-7. doi: 10.1111/1523-1747.ep12456946.
In earlier studies, it was shown that the human plasma-spreading glycoprotein, epibolin (the 65 kD species of serum-spreading factor or vitronectin), requires a second plasma component, termed coepibolin, in order to support maximal dissociated epidermal cell spreading in tissue culture. Whereas epibolin alone in defined medium supports some cell spreading, the purified plasma coepibolin preparations do not effect spreading in the absence of epibolin. Although not yet entirely purified, coepibolin associates with some plasma fractions but not with others; it is certainly not a property of all proteins, e.g., while bovine serum albumin (BSA) has coepibolin activity, ovalbumin does not. The data presented here show that the phorbol ester, 12-tetra-decanoyl-1-phorbol-13-acetate (TPA) can act as a potent coepibolin and support maximal spreading over a concentration range of 10-100 ng/ml. In the absence of epibolin TPA does not stimulate the spreading of epidermal cells when given alone or in the presence of BSA or ovalbumin. Coepibolin activity appears to associate with tumor-promoting activity in that the phorbol derivative, phorbol-12,13-didecanoate, shows coepibolin activity, while its inactive non-tumor-promoting isomer, phorbol-4 alpha-phorbol-12,13-didecanoate, does not. These data suggest that the proteinaceous plasma-derived cofactor acts in a fashion similar to TPA and that this as yet unexplained mechanism of TPA action is important to the full expression of epibolin and to the early phase of epidermal cell spreading.
在早期研究中发现,人血浆扩散糖蛋白表皮生成素(血清扩散因子或玻连蛋白的65kD种类),为了在组织培养中支持最大程度的解离表皮细胞扩散,需要第二种血浆成分,称为共表皮生成素。虽然在限定培养基中单独的表皮生成素能支持一些细胞扩散,但纯化的血浆共表皮生成素制剂在没有表皮生成素时不会影响扩散。尽管尚未完全纯化,但共表皮生成素与一些血浆组分结合,而与其他组分不结合;它肯定不是所有蛋白质的特性,例如,牛血清白蛋白(BSA)具有共表皮生成素活性,而卵清蛋白则没有。此处给出的数据表明,佛波酯12 - 十四烷酰佛波醇-13 - 乙酸酯(TPA)可作为一种有效的共表皮生成素,并在10 - 100 ng/ml的浓度范围内支持最大程度的扩散。在没有表皮生成素的情况下,单独给予TPA或在有BSA或卵清蛋白存在时,TPA都不会刺激表皮细胞的扩散。共表皮生成素活性似乎与肿瘤促进活性相关,因为佛波醇衍生物佛波醇-12,13 - 二癸酸酯具有共表皮生成素活性,而其无活性的非肿瘤促进异构体佛波醇-4α-佛波醇-12,13 - 二癸酸酯则没有。这些数据表明,源自血浆的蛋白质辅因子的作用方式与TPA类似,并且TPA这种尚未得到解释的作用机制对于表皮生成素的充分表达以及表皮细胞扩散的早期阶段很重要。