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三维与二维皮肤免疫彗星芯片筛选局部毒物和皮肤特异性细胞色素诱导剂。

Skin Immuno-CometChip in 3D vs. 2D Cultures to Screen Topical Toxins and Skin-Specific Cytochrome Inducers.

机构信息

Department of Biochemistry and Molecular & Cellular Biology, Georgetown University School of Medicine, Washington, DC 20057, USA.

Amelia Technologies, LLC, Washington, DC 20001, USA.

出版信息

Genes (Basel). 2023 Mar 2;14(3):630. doi: 10.3390/genes14030630.

Abstract

The targets of topical genotoxic agents are basal and stem cells of the skin. These cells may misrepair DNA lesions, resulting in deleterious mutations of tumor suppressors or oncogenes. However, the genotoxicity of many compounds has not as yet been determined and needs to be tested using a relevant skin model. To this end, we designed a new high-throughput assay for the detection of agents that create DNA damage in epidermal stem and basal cells and used it to test known DNA-damaging agents. We utilized either 2D epidermal cells or 3D skin equivalents and topically exposed them to different compounds. The Skin Immuno-CometChip assay uses arrays of microwells formed in a collagen/agarose mixture to capture single basal cells in each microwell by virtue of collagen binding to α2β1 integrin, which is present only on basal and stem cells. The presence of β1 integrin was verified by immunofluorescent labeling cells that were then subjected to an electrical field, allowing for the migration of nicked DNA out of the nucleoid in alkali, with the resulting DNA comets stained and imaged. Furthermore, using improved comet detection software allowed for the automated and rapid quantification of DNA damage. Our study indicates that we can accurately predict genotoxicity by using 3D skin cultures, as well as keratinocytes grown in 2D monolayers.

摘要

局部遗传毒性药物的作用靶点是皮肤的基底细胞和干细胞。这些细胞可能会错误修复 DNA 损伤,导致肿瘤抑制因子或癌基因的有害突变。然而,许多化合物的遗传毒性尚未确定,需要使用相关的皮肤模型进行测试。为此,我们设计了一种新的高通量检测表皮干细胞和基底细胞中产生 DNA 损伤的药物的方法,并将其用于测试已知的 DNA 损伤药物。我们利用 2D 表皮细胞或 3D 皮肤等效物,并将其局部暴露于不同的化合物中。Skin Immuno-CometChip 检测法利用胶原蛋白/琼脂糖混合物中形成的微井阵列,通过胶原蛋白与仅存在于基底细胞和干细胞上的 α2β1 整合素结合,捕获每个微井中的单个基底细胞。β1 整合素的存在通过免疫荧光标记细胞进行验证,然后对这些细胞施加电场,使核小体中的切口 DNA 在碱性条件下迁移,用彗星染色和成像来检测产生的 DNA 彗星。此外,使用改进的彗星检测软件可以自动快速地定量 DNA 损伤。我们的研究表明,我们可以通过使用 3D 皮肤培养物以及在 2D 单层中培养的角质形成细胞来准确预测遗传毒性。

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