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视黄酸上调正常人表皮角质形成细胞 P2Y2 受体。

Upregulation of P2Y2 receptors by retinoids in normal human epidermal keratinocytes.

机构信息

Division of Biosignaling, National Institute of Health Science, 1-18-1 Kamiyoga, Setagaya, Tokyo, Japan.

出版信息

Purinergic Signal. 2006 Sep;2(3):491-8. doi: 10.1007/s11302-005-7331-5. Epub 2006 Aug 11.

Abstract

Retinoids, vitamin A derivatives, are important regulators of the growth and differentiation of skin cells. Although retinoids are therapeutically used for several skin ailments, little is known about their effects on P2 receptors, known to be involved in various functions in the skin. DNA array analysis showed that treatment of normal human epidermal keratinocytes (NHEKs) with all-trans-retinoic acid (ATRA), an agonist to RAR (retinoic acid receptor), enhanced the expression of mRNA for the P2Y2 receptor, a metabotropic P2 receptor that is known to be involved in the proliferation of the epidermis. The expression of other P2 receptors in NHEKs was not affected by ATRA. ATRA increased the mRNA for the P2Y2 receptor in a concentration-dependent fashion (1 nM to 1 muM). Am80, a synthesized agonist to RAR, showed a similar enhancement, whereas 9-cis-retinoic acid (9-cisRA), an agonist to RXR (retinoid X receptor), enhanced P2Y2 gene expression to a lesser extent. Ca(2+) imaging analysis showed that ATRA also increased the function of P2Y2 receptors in NHEKs. Retinoids are known to enhance the turnover of the epidermis by increasing both proliferation and terminal differentiation. The DNA microarray analysis also revealed that ATRA upregulates various genes involved in the differentiation of NHEKs. Our present results suggest that retinoids, at least in part, exert their proliferative effects by upregulating P2Y2 receptors in NHEKs. This effect of retinoids may be closely related to their therapeutic effect against various ailments or aging events in skins such as over-keratinization, pigmentation and re-modeling.

摘要

视黄醇类,维生素 A 的衍生物,是皮肤细胞生长和分化的重要调节剂。尽管视黄醇类药物被用于治疗多种皮肤疾病,但人们对它们对 P2 受体的影响知之甚少,已知 P2 受体参与皮肤的各种功能。DNA 芯片分析显示,全反式视黄酸(ATRA),一种 RAR(视黄酸受体)激动剂,处理正常人表皮角质形成细胞(NHEKs)可增强 P2Y2 受体的 mRNA 表达,P2Y2 受体是一种代谢型 P2 受体,已知参与表皮增殖。ATRA 不影响 NHEKs 中其他 P2 受体的表达。ATRA 以浓度依赖的方式增加 P2Y2 受体的 mRNA(1 nM 至 1 μM)。Am80,一种合成的 RAR 激动剂,表现出相似的增强作用,而 9-顺式视黄酸(9-cisRA),一种 RXR(视黄醇 X 受体)激动剂,对 P2Y2 基因表达的增强作用较小。钙成像分析显示 ATRA 也增加了 NHEKs 中 P2Y2 受体的功能。视黄醇类药物通过增加增殖和终末分化来增强表皮的更新。DNA 微阵列分析还表明,ATRA 上调了 NHEKs 中参与分化的各种基因。我们目前的结果表明,视黄醇类药物至少部分通过上调 NHEKs 中的 P2Y2 受体发挥其增殖作用。这种视黄醇类药物的作用可能与其治疗各种皮肤疾病或老化事件的疗效密切相关,如过度角化、色素沉着和重塑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c7/2104003/bfbf2dbcdbff/11302_2005_Article_7331_Fig1.jpg

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