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在气液界面培养的人角质形成细胞培养物的屏障功能。

Barrier function of human keratinocyte cultures grown at the air-liquid interface.

作者信息

Mak V H, Cumpstone M B, Kennedy A H, Harmon C S, Guy R H, Potts R O

机构信息

Department of Pharmacy, University of California, San Francisco.

出版信息

J Invest Dermatol. 1991 Mar;96(3):323-7. doi: 10.1111/1523-1747.ep12465212.

Abstract

Stratum corneum (SC), the outermost and least permeable layer of skin, is the major barrier to passive transepidermal water loss. In the research described in this paper, we have used human keratinocyte cultures, grown at the air-liquid (A/L) interface, to examine the relationship between epidermal differentiation (including SC formation) and barrier function. Histologically, the A/L culture showed several markers of complete differentiation, including the presence of well-organized and defined epidermal cell layers, keratohyalin granules, and a multilayered SC. The permeability of tritiated water through epidermal cultures, which had grown for 3 weeks at the A/L interface, was measured with a microdiffusion apparatus. The results of these experiments demonstrated that: a) the human keratinocyte cultures developed a substantial barrier (i.e., a multilayered SC) to water diffusion across the entire surface. If the relative humidity of the culturing environment was lowered from 100% to around 75%, the barrier was significantly improved; b) the differentiation promoter, 1.25-dihydroxy-vitamin-D3, increased the number of SC layers and reduced water permeation through the culture; c) the nature of the keratinocyte support matrix could be altered to improve the morphology as well as the barrier function of the epidermal cultures. Overall, the observations are consistent with the relationship that is believed to exist between SC intercellular lipid content and percutaneous penetration. Confirmation of this hypothesis will further the considerable potential of human keratinocyte A/L cultures as a valuable and relevant model in which to study drug absorption and metabolism.

摘要

角质层(SC)是皮肤最外层且渗透性最低的一层,是被动经表皮水分流失的主要屏障。在本文所述的研究中,我们使用了在气液(A/L)界面生长的人角质形成细胞培养物,来研究表皮分化(包括SC形成)与屏障功能之间的关系。组织学上,A/L培养物显示出几种完全分化的标志物,包括组织结构良好且明确的表皮细胞层、透明角质颗粒和多层SC的存在。使用微扩散装置测量了在A/L界面生长3周的表皮培养物对氚标记水的渗透性。这些实验结果表明:a)人角质形成细胞培养物在整个表面形成了对水扩散的实质性屏障(即多层SC)。如果将培养环境的相对湿度从100%降低到约75%,屏障会显著改善;b)分化促进剂1,25 - 二羟基维生素D3增加了SC层数并降低了水通过培养物的渗透率;c)可以改变角质形成细胞支持基质的性质,以改善表皮培养物的形态以及屏障功能。总体而言,这些观察结果与SC细胞间脂质含量与经皮渗透之间被认为存在的关系一致。对这一假设的证实将进一步提升人角质形成细胞A/L培养物作为研究药物吸收和代谢的有价值且相关模型的巨大潜力。

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