Zalacain M, Sierrasesúmaga L, Patiño A
Laboratorio de Pediatría, Universidad de Navarra, Pamplona, 31080, Spain.
An Sist Sanit Navar. 2005 May-Aug;28(2):227-36. doi: 10.4321/s1137-66272005000300007.
Human genetic integrity is compromised by the intense industrial activity, which emphasizes the importance to determine an "acceptable" genetic damage level and to carry out routine genotoxicity assays in the populations at risk. Micronuclei are cytoplasmatic bodies of nuclear origin which correspond to genetic material that is not correctly incorporated in the daughter cells in the cellular division; they reflect the existence of chromosomal aberrations and are originated by chromosomal breaks, replication errors followed by cellular division of the DNA and/or exposure to genotoxic agents. There are several factors able to modify the number of micronuclei present in a given cell, among them are age, gender, vitamins, medical treatments, daily exposure to genotoxic agents, etc. The cytogenetic assay for the detection of micronuclei (CBMN: cytokinesis-block micronucleus) is based on the use of a chemical agent, cytochalasin-B, which is able to block cytocinesis but allowing the nuclear division, therefore yielding binucleated and monodivided cells. The micronuclei scoring is performed on 1000 binucleated cells and the starting sample may vary, although most studies are performed on peripheral blood lymphocytes. The micronuclei assay is considered a practical, universally validated and technically feasible protocol which is useful to evaluate the genetic instability induced by genotoxic agents.
高强度的工业活动损害了人类的基因完整性,这凸显了确定“可接受”的基因损伤水平以及对高危人群进行常规基因毒性检测的重要性。微核是源于细胞核的细胞质体,对应于细胞分裂时未正确整合到子细胞中的遗传物质;它们反映了染色体畸变的存在,由染色体断裂、DNA细胞分裂后的复制错误和/或接触基因毒性剂引起。有几个因素能够改变给定细胞中微核的数量,其中包括年龄、性别、维生素、医疗治疗、日常接触基因毒性剂等。用于检测微核的细胞遗传学检测方法(CBMN:胞质分裂阻断微核法)基于使用一种化学试剂细胞松弛素B,它能够阻断胞质分裂但允许核分裂,从而产生双核和单核分裂细胞。微核计数是在1000个双核细胞上进行的,起始样本可能会有所不同,尽管大多数研究是在外周血淋巴细胞上进行的。微核检测被认为是一种实用、普遍验证且技术上可行的方案,有助于评估基因毒性剂诱导的基因不稳定。