Métézeau P
Institut Pasteur, Unité de Biochimie des Régulations Cellulaires, Paris, France.
Pathol Biol (Paris). 1988 Jan;36(1):46-51.
Human chromosomes can be observed after coloration with ADN specific fluorochromes. Measurement of fluorescence intensity may be done by flow cytometry and it allows achievement of flow karyotypes. It is possible to define a standard karyotype and-by comparison-to bring to the fore chromosomes abnormalities (translocation, deletion, polysomy). Various genomic abnormalities are observed with leukemia. Flow cytometry allows a multiparameter analysis which could be used to detect rare events, unknown in classic karyotyping. With Flow Cytometry and cell sorting, the abnormal chromosomes could be separated and secondly observed after Q banding or analysed after molecular hybridization to confirm leukemia diagnosis or prognostic. Flow cytometry, an analytical technology already used in onco-hematology, allows, which chromosome analysis associated with other technics (molecular biology,...) a new approach of particular diagnosis.
用特异性的DNA荧光染料染色后可观察到人类染色体。可通过流式细胞术测量荧光强度,进而获得流式核型。有可能确定标准核型,并通过比较发现染色体异常(易位、缺失、多体性)。白血病患者可观察到各种基因组异常。流式细胞术可进行多参数分析,用于检测经典核型分析中未知的罕见事件。通过流式细胞术和细胞分选,可分离出异常染色体,其次在Q显带后观察或在分子杂交后进行分析,以确诊白血病或判断预后。流式细胞术是一种已应用于肿瘤血液学的分析技术,它与其他技术(分子生物学等)相结合进行染色体分析,为特殊诊断提供了一种新方法。