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在正常人表皮角质形成细胞中敲低多囊蛋白1(PKD1)可增加角蛋白10和兜甲蛋白的mRNA表达:角质形成细胞分化的早期标志物。

Knockdown of PKD1 in normal human epidermal keratinocytes increases mRNA expression of keratin 10 and involucrin: early markers of keratinocyte differentiation.

作者信息

Ivanova Petya, Atanasova Ganka, Poumay Yves, Mitev Vanyo

机构信息

Department Chemistry and Biochemistry, Medical University, Sofia, Bulgaria.

出版信息

Arch Dermatol Res. 2008 Mar;300(3):139-45. doi: 10.1007/s00403-008-0832-7. Epub 2008 Feb 8.

DOI:10.1007/s00403-008-0832-7
PMID:18259765
Abstract

Subconfluent normal human keratinocytes exhibit autonomous (autocrine growth factor driven) proliferation and express the specific markers for keratinocyte proliferation K5 (keratin 5) and K14 (keratin 14). Utilizing this model the effects of PKD1 (Protein kinase D1) knockdown on activation of differentiation was studied. siRNA approach was applied to achieve specific knockdown of PKD1 and the mRNA levels of different keratinocyte markers -- K14 and PCNA (markers of basal proliferating keratinocytes), involucrin and K10 (early differentiation markers) were analyzed. Treatment of cultured keratinocytes with siRNA for PKD1 resulted in reduction of mRNA levels of PKD1, altered cell phenotype and promotion of keratinocyte differentiation, demonstrated by increased expression of involucrin and K10 mRNAs. No significant changes in K14 mRNA expression levels were detected, but the expression of PCNA mRNA was markedly diminished. This study was the first to show that mRNA expression of PKD1 in subconfluent normal human keratinocytes is very low, the PKD1 mRNA levels were more than 8-fold lower than the same ones in hTert keratinocytes. These findings suggest antidifferentiative role of PKD1 in normal human keratinocytes, contrary to the prodiferentiative role of PKD1 in human hTert keratinocytes. We came to the conclusion that there are differences between transduction pathways involving PKD1 in primary human keratinocyte cultures and these in immortalized hTert keratinocytes.

摘要

亚汇合状态的正常人角质形成细胞表现出自主(自分泌生长因子驱动)增殖,并表达角质形成细胞增殖的特异性标志物K5(角蛋白5)和K14(角蛋白14)。利用该模型研究了PKD1(蛋白激酶D1)敲低对分化激活的影响。应用siRNA方法实现PKD1的特异性敲低,并分析了不同角质形成细胞标志物——K14和PCNA(基底增殖角质形成细胞的标志物)、兜甲蛋白和K10(早期分化标志物)的mRNA水平。用PKD1的siRNA处理培养的角质形成细胞导致PKD1的mRNA水平降低、细胞表型改变以及角质形成细胞分化的促进,这通过兜甲蛋白和K10 mRNA表达的增加得以证明。未检测到K14 mRNA表达水平的显著变化,但PCNA mRNA的表达明显减少。该研究首次表明,亚汇合状态的正常人角质形成细胞中PKD1的mRNA表达非常低,PKD1的mRNA水平比hTert角质形成细胞中的低8倍以上。这些发现表明PKD1在正常人角质形成细胞中具有抗分化作用,这与PKD1在人hTert角质形成细胞中的促增殖作用相反。我们得出结论,原代人角质形成细胞培养物中涉及PKD1的转导途径与永生化hTert角质形成细胞中的转导途径存在差异。

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