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激动素诱导体外衰老的正常人角质形成细胞分化。

Kinetin-induced differentiation of normal human keratinocytes undergoing aging in vitro.

作者信息

Berge Ulrich, Kristensen Peter, Rattan Suresh I S

机构信息

Laboratory of Cellular Ageing, Danish Centre for Molecular Gerontology, Department of Molecular Biology, University of Aarhus, Denmark.

出版信息

Ann N Y Acad Sci. 2006 May;1067:332-6. doi: 10.1196/annals.1354.045.

Abstract

Kinetin (N(6)-furfuryladenine) is a cytokinin growth factor having several anti-aging effects reported for human cells and fruit flies. We have observed that short-term culturing of human keratinocytes in the presence of 40 to 200 microM kinetin results in a significant inhibition of cell growth. Studies were undertaken to analyze the process of differentiation as a reason for growth inhibition. Keratinocytes at different passage levels were treated with fetal calf serum (FCS) and calcium as differentiation-inducing positive controls, with different concentrations of kinetin, and with a combination of kinetin and calcium. The induction and progression of differentiation was monitored by morphological observations and by using several differentiation markers, including keratins (K10 and K14), involucrin, epidermal transglutaminase, and some new keratinocyte-specific antibodies isolated by the phage display method. In young keratinocytes, two days of calcium treatment reduced the K14 level by 78%, and increased the levels of K10 and involucrin by 40% and 29%, respectively. In comparison, 40 microM kinetin had no effect on the K14 level, but increased the K10 level by 28% and that of involucrin by four-fold. The combination of calcium and 40 microM kinetin led to a decrease by 23% in the K14 level, to an increase in the level of K10 by 55%, and to a two-fold rise in the involucrin level. These results suggest that the rate, extent, and quality of differentiation depend on the inducing agent, and that kinetin may be useful in promoting the differentiation of human keratinocytes, especially in the presence of calcium.

摘要

激动素(N⁶-糠基腺嘌呤)是一种细胞分裂素生长因子,据报道对人类细胞和果蝇具有多种抗衰老作用。我们观察到,在40至200微摩尔激动素存在的情况下对人角质形成细胞进行短期培养会导致细胞生长受到显著抑制。开展了研究以分析分化过程作为生长抑制的原因。用胎牛血清(FCS)和钙作为诱导分化的阳性对照、不同浓度的激动素以及激动素与钙的组合处理不同传代水平的角质形成细胞。通过形态学观察以及使用多种分化标志物来监测分化的诱导和进程,这些标志物包括角蛋白(K10和K14)、内披蛋白、表皮转谷氨酰胺酶以及一些通过噬菌体展示法分离的新的角质形成细胞特异性抗体。在年轻的角质形成细胞中,两天的钙处理使K14水平降低了78%,使K10和内披蛋白水平分别提高了40%和29%。相比之下,40微摩尔激动素对K14水平没有影响,但使K10水平提高了28%,使内披蛋白水平提高了四倍。钙与40微摩尔激动素的组合导致K14水平降低了23%,K10水平提高了55%,内披蛋白水平提高了两倍。这些结果表明,分化的速率、程度和质量取决于诱导剂,并且激动素可能有助于促进人角质形成细胞的分化,尤其是在有钙存在的情况下。

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