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Effect of RNA interference of tight junction-related molecules on intercellular barrier function in cultured human keratinocytes
被引:0
|作者:
Takuya Yamamoto
Yuko Saeki
Masumi Kurasawa
Shohei Kuroda
Seiji Arase
Hiroyuki Sasaki
机构:
[1] The University of Tokushima Graduate School,Department of Dermatology, Institute of Health Biosciences
[2] Pola Chemical Industries Inc.,Department of Molecular Cell Biology
[3] Institute of DNA Medicine,undefined
[4] The Jikei University School of Medicine,undefined
来源:
关键词:
Tight junction;
Occludin;
Claudin-1;
Human epidermal keratinocyte;
Small interfering RNA;
Transepithelial electrical resistance;
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摘要:
Accumulating evidence shows that tight junctions (TJs) in the granular layer contribute to the epidermal barrier, suggesting that the regulation of TJ assembly in keratinocytes may provide a clue to understanding the role of barrier formation in epidermis. In this study, we investigated the behavior of TJ-related molecules in cultured human keratinocytes during keratinization induced by transfer to high-calcium medium, and the effect of RNA interference of TJ-related molecules on intercellular permeability and morphological features. The expression of TJ-related molecules and transepithelial electrical resistance were increased by transfer to high-calcium medium. In cells under the same conditions, we observed by freeze-fracture electron microscopy that TJ strands developed on the apposing cell membranes. In contrast, the transepithelial electrical resistance was clearly suppressed when the expression of claudin-1 or occludin was blocked by RNA interference. The morphological features of these knock-down cells were the same as those of MOCK cells, except for a marked decrease in the number of TJ strands. Furthermore, claudin-1 suppression inhibited occludin localization at the cell membrane, whereas suppression of occludin did not influence the localization of claudin-1. These results suggest that claudin-1 plays a crucial role in recruiting occludin to TJs, and that occludin is involved in intercellular barrier function.
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页码:517 / 524
页数:7
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