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一种双重荧光染色方法提高了胞质分裂阻断微核试验的灵敏度。

A Double Fluorescent Staining Method Increases the Sensitivity of the Cytokinesis-Block Micronucleus Assay.

作者信息

Udroiu Ion

机构信息

Dipartimento di Scienze, Università degli Studi "Roma Tre", 00146 Rome, Italy.

出版信息

Methods Protoc. 2025 Jan 4;8(1):3. doi: 10.3390/mps8010003.

Abstract

The micronucleus test is one of the most popular genotoxicity assays. In order to avoid underestimation of micronuclei frequencies by counting non-replicating cells, the cytokinesis-blocked micronucleus test has been developed. In this technique, only binucleated cells are scored. One underestimated problem is the potential difficulty in discriminating binucleated from mononucleated cells when using DAPI staining, i.e., the possibility that two neighboring mononucleated cells could be mistaken for a binucleated one. The new protocol presented here comprises the addition of acridine orange in order to stain the cytoplasm (in addition to DAPI to stain nuclei and micronuclei). This new technique can increase the sensitivity of the cytokinesis-blocked micronucleus test and avoid underestimation of micronuclei frequencies, an important issue when high doses are employed.

摘要

微核试验是最常用的遗传毒性检测方法之一。为避免因对非复制细胞计数而低估微核频率,人们开发了胞质分裂阻滞微核试验。在该技术中,仅对双核细胞进行评分。一个被低估的问题是,使用4′,6-二脒基-2-苯基吲哚(DAPI)染色时,区分单核细胞和双核细胞可能存在潜在困难,即两个相邻单核细胞可能被误认作双核细胞。本文介绍的新方案包括添加吖啶橙以对细胞质进行染色(除了用DAPI对细胞核和微核进行染色)。这项新技术可以提高胞质分裂阻滞微核试验的灵敏度,避免微核频率被低估,这在使用高剂量时是一个重要问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8139/11755469/e7235d6c6d8a/mps-08-00003-g001.jpg

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