G2修复与衰老:供体年龄对人淋巴细胞染色体畸变的影响

J. Pincheira , C. Gallo , M. Bravo , M.H. Navarrete , J.F. Lopez-Saez
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引用次数: 33

摘要

研究了咖啡因对三组正常供体人淋巴细胞染色体畸变频率和平均G2持续时间的影响。II: 30-40岁;III: 60-70岁)。在对照条件下,三个年龄组显示出相似的染色体畸变频率。所有三个年龄组对咖啡因治疗的畸变表现出线性剂量反应。然而,老年个体(II组和III组)的淋巴细胞比年轻个体(I组)的细胞表现出更高的染色体畸变频率和更长的G2持续时间。咖啡因在减少G2长度方面的作用在每个年龄组中都相当相似。在老年人淋巴细胞中,腺苷或烟酰胺对咖啡因作用的逆转作用高于第一组。老年人和年轻人淋巴细胞中咖啡因作用和G2值的不同,很可能是由于老年人淋巴细胞中DNA损伤达到G2期的数量较多和/或G2修复能力的降低。
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G2 repair and aging: influence of donor age on chromosomal aberrations in human lymphocytes

The caffeine effects on chromosomal aberration frequency and mean G2 duration were studied in human lymphocytes in vitro from three age groups of normal donors (I: 1–5 years old; II: 30–40 years old; III: 60–70 years old). Under control conditions, the three age group showed a similar frequency of chromosomal aberrations. All three age groups exhibited a linear dose response for aberrations with caffeine treatments. However, lymphocytes from aged individuals (groups II and III) showed higher chromosomal aberration frequencies and longer G2 duration than cells from young individuals (group I). The caffeine effect in reducing G2 length was rather similar in every age group. The reversion of caffeine effects by adenosine or niacinamide in lymphocytes from older individuals was higher than in cells from group I. The different caffeine effects and G2 values between lymphocytes from old and young individuals are most likely due to a higher number of DNA lesions reaching G2 phase and/or a decrease of the G2 repair capability of lymphocytes from older individuals.

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