Moreira C F A, Brito L C, Lemos J A R
Universidade Federal do Pará, Instituto de Ciências Biológicas, Belém, PA, Brasil.
Genet Mol Res. 2008;7(4):1353-9. doi: 10.4238/vol7-4gmr510.
The main feature of Fanconi anemia (FA) is the high sensitivity of the cells to the clastogenic agent, diepoxybutane (DEB). Thus, differential diagnosis of this syndrome can be made by cytogenetic analysis; adding DEB to lymphocytes in culture (DEB test) increases the number of chromosome breaks. Fanconi anemia cells have an abnormal cell cycle, with an increased frequency of cells arrested at G2. In order to determine if flow cytometry can be utilized for FA diagnosis, we cultivated lymphocytes with DEB and analyzed them for G2 accumulation. Lymphocytes cultivated for 72 h were labeled with CD3 antibody and propidium iodide for analysis of the cells in the G2 phase. Cultures of lymphocytes from two FA patients who were diagnosed by the DEB test and six control individuals with a negative DEB test had 55.26% (SD +/- 6.97) and 2.81% (SD +/- 0.22) cells arrested at G2, respectively. We conclude that flow-cytometry analysis of cells exposed to DEB can be useful for FA diagnosis.
范可尼贫血(FA)的主要特征是细胞对致断裂剂二环氧丁烷(DEB)高度敏感。因此,该综合征的鉴别诊断可通过细胞遗传学分析进行;在培养的淋巴细胞中添加DEB(DEB试验)会增加染色体断裂的数量。范可尼贫血细胞具有异常的细胞周期,停滞在G2期的细胞频率增加。为了确定流式细胞术是否可用于FA诊断,我们用DEB培养淋巴细胞并分析其G2期积累情况。培养72小时的淋巴细胞用CD3抗体和碘化丙啶标记,用于分析G2期的细胞。通过DEB试验诊断的两名FA患者和六名DEB试验阴性的对照个体的淋巴细胞培养物中,分别有55.26%(标准差±6.97)和2.81%(标准差±0.22)的细胞停滞在G2期。我们得出结论,对暴露于DEB的细胞进行流式细胞术分析可用于FA诊断。