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使用特异性抗体对紫外线诱导的DNA损伤进行定量和可视化:在色素细胞生物学中的应用

Quantitation and visualization of ultraviolet-induced DNA damage using specific antibodies: application to pigment cell biology.

作者信息

Kobayashi N, Katsumi S, Imoto K, Nakagawa A, Miyagawa S, Furumura M, Mori T

机构信息

Department of Dermatology, Nara Medical University, Kashihara, Japan.

出版信息

Pigment Cell Res. 2001 Apr;14(2):94-102. doi: 10.1034/j.1600-0749.2001.140204.x.

DOI:10.1034/j.1600-0749.2001.140204.x
PMID:11310797
Abstract

The major types of DNA damage induced by sunlight in the skin are DNA photoproducts, such as cyclobutane pyrimidine dimers (CPDs), (6-4)photoproducts (6-4PPs) and Dewar isomers of 6-4PPs. A sensitive method for quantitating and visualizing each type of DNA photoproduct induced by biologically relevant doses of ultraviolet (UV) or sunlight is essential to characterize DNA photoproducts and their biological effects. We have established monoclonal antibodies specific for CPDs, 6-4PPs or Dewar isomers. Those antibodies allow one to quantitate photoproducts in DNA purified from cultured cells or from the skin epidermis using an enzyme-linked immunosorbent assay. One can also use those specific antibodies with in situ laser cytometry to visualize and measure DNA photoproducts in cultured cells or in the skin, using indirect immunofluorescence and a laser-scanning confocal microscope. This latter method allows us to reconstruct three-dimensional images of nuclei containing DNA photoproducts and to simultaneously examine DNA photoproducts and histology in multilayered epidermis. Using those techniques, one can determine the induction and repair of these three distinct types of DNA photoproducts in cultured cells and in the skin exposed to sublethal or suberythematous doses of UV or solar simulated radiation. As examples of the utility of these techniques and antibodies, we describe the DNA repair kinetics following irradiation of human cell nuclei and the photoprotective effect of melanin against DNA photoproducts in cultured pigmented cells and in human epidermis.

摘要

阳光在皮肤中诱导产生的主要DNA损伤类型是DNA光产物,如环丁烷嘧啶二聚体(CPD)、(6-4)光产物(6-4PP)以及6-4PP的杜瓦异构体。一种用于定量和可视化由生物学相关剂量的紫外线(UV)或阳光诱导产生的每种DNA光产物的灵敏方法,对于表征DNA光产物及其生物学效应至关重要。我们已经制备了针对CPD、6-4PP或杜瓦异构体的单克隆抗体。这些抗体能够使人们利用酶联免疫吸附测定法定量从培养细胞或皮肤表皮中纯化出的DNA中的光产物。人们还可以将这些特异性抗体与原位激光细胞仪结合使用,通过间接免疫荧光和激光扫描共聚焦显微镜来可视化并测量培养细胞或皮肤中的DNA光产物。后一种方法使我们能够重建含有DNA光产物的细胞核的三维图像,并同时检查多层表皮中的DNA光产物和组织学情况。利用这些技术,人们可以确定在培养细胞以及暴露于亚致死或亚红斑剂量的UV或太阳模拟辐射的皮肤中这三种不同类型DNA光产物的诱导和修复情况。作为这些技术和抗体实用性的实例,我们描述了照射人细胞核后的DNA修复动力学以及黑色素对培养的色素细胞和人表皮中DNA光产物的光保护作用。

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