首页> 外文期刊>Archives of dermatological research. >Knockdown of PKD1 in normal human epidermal keratinocytes increases mRNA expression of keratin 10 and involucrin: early markers of keratinocyte differentiation.
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Knockdown of PKD1 in normal human epidermal keratinocytes increases mRNA expression of keratin 10 and involucrin: early markers of keratinocyte differentiation.

机译:正常人表皮角质形成细胞中PKD1的敲低可增加角蛋白10和involucrin的mRNA表达:角质形成细胞分化的早期标志物。

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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 normalhuman 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.
机译:次汇合的正常人角质形成细胞表现出自主性(自分泌生长因子驱动的)增殖,并表达角质形成细胞增殖的特异性标记物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。 siRNA方法用于实现PKD1的特异性敲低,并分析了不同的角质形成细胞标志物K14和PCNA(基底增殖性角化细胞标志物),整合素和K10(早期分化标志物)的mRNA水平。 siRNA处理PKD1对培养的角质形成细胞的作用导致PKD1的mRNA水平降低,细胞表型改变和角质形成细胞分化的促进,这主要是通过整合素和K10 mRNA的表达增加所证实的。没有检测到K14 mRNA表达水平的显着变化,但是PCNA mRNA的表达显着降低。这项研究首次表明,亚汇合的正常人角质形成细胞中PKD1的mRNA表达非常低,PKD1 mRNA的水平比hTert角质形成细胞中的PKD1 mRNA低8倍以上。这些发现表明PKD1在正常人角质形成细胞中的抗分化作用,与PKD1在人hTert角质形成细胞中的增生作用相反。我们得出的结论是,涉及PKD1的转导途径在原代人角质形成细胞培养物中和永生化的hTert角质形成细胞中存在差异。

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