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角质形成细胞衍生因子对人黑素细胞生长、树突形成及黑素化的调节

Regulation of human melanocyte growth, dendricity, and melanization by keratinocyte derived factors.

作者信息

Gordon P R, Mansur C P, Gilchrest B A

机构信息

USDA Human Nutrition Research Center on Aging, Tufts University, Boston, Massachusetts 02111.

出版信息

J Invest Dermatol. 1989 Apr;92(4):565-72. doi: 10.1111/1523-1747.ep12709595.

Abstract

Epidermal pigmentation involves the synthesis of melanin in melanocytes and its transfer to surrounding keratinocytes, where it functions in photoprotection. To investigate the possible role of the keratinocyte in regulating pigmentation, human keratinocytes were incubated for 24 h in a defined culture medium, which was then transferred to pure human melanocyte cultures. After 1 week, the conditioned medium produced a fourfold increase in melanocyte yield and a seven-fold increase in total melanin. Increased melanocyte dendricity was clearly visible within 24 h as well. Ultrafiltration of the keratinocyte-conditioned medium suggested approximately one-half of the growth promoting activity as well as most of the dendricity and melanization stimulating activities were of low molecular weight (less than 500 Da). High molecular weight fractions stimulated only melanocyte growth. Of the several known keratinocyte-derived factors tested, none could be implicated as a mediator of the observed effects. Basic fibroblast growth factor, known to stimulate melanocyte growth in some culture systems, failed to stimulate growth, dendricity, or melanin content when added to the complete non-conditioned medium. Interleukin-1 alpha, interleukin-1 beta, 12-hydroxyeicosatetraenoic acid, prostaglandin E2, leukotriene B4, and adenosine 3',5'-cyclic monophosphate analogues also had no effect. These studies demonstrate that keratinocytes in vitro release factors that modulate melanocyte behavior and expand our understanding of controls for human epidermal pigmentation.

摘要

表皮色素沉着涉及黑素细胞中黑色素的合成及其向周围角质形成细胞的转移,黑色素在角质形成细胞中发挥光保护作用。为了研究角质形成细胞在调节色素沉着中的可能作用,将人角质形成细胞在特定培养基中培养24小时,然后将该培养基转移至纯人黑素细胞培养物中。1周后,条件培养基使黑素细胞产量增加了四倍,总黑色素增加了七倍。在24小时内也明显可见黑素细胞树突增多。对角质形成细胞条件培养基进行超滤表明,大约一半的促生长活性以及大部分树突增多和黑素化刺激活性是低分子量的(小于500道尔顿)。高分子量组分仅刺激黑素细胞生长。在测试的几种已知的角质形成细胞衍生因子中,没有一种可被认为是观察到的效应的介质。已知在某些培养系统中刺激黑素细胞生长的碱性成纤维细胞生长因子,添加到完全无血清培养基中时,未能刺激生长、树突增多或黑色素含量。白细胞介素-1α、白细胞介素-1β、12-羟基二十碳四烯酸、前列腺素E2、白三烯B4和腺苷3',5'-环磷酸类似物也没有作用。这些研究表明,体外培养的角质形成细胞释放调节黑素细胞行为的因子,扩展了我们对人类表皮色素沉着控制的理解。

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