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人类的“自发性”基因损伤:个体间变异性评估、损伤标记物之间的关系以及营养状况的影响

'Spontaneous' genetic damage in man: evaluation of interindividual variability, relationship among markers of damage, and influence of nutritional status.

作者信息

MacGregor J T, Wehr C M, Hiatt R A, Peters B, Tucker J D, Langlois R G, Jacob R A, Jensen R H, Yager J W, Shigenaga M K, Frei B, Eynon B P, Ames B N

机构信息

SRI International, Menlo Park, CA 94025-3493, USA.

出版信息

Mutat Res. 1997 Jun 9;377(1):125-35. doi: 10.1016/s0027-5107(97)00070-5.

Abstract

The 'spontaneous' frequency of genetic damage (normal background) and the possible relationship of this damage to nutritional variables in humans were investigated in 22 subjects using several indices of genetic damage. The subjects were chosen, out of 122 initially analyzed, for being at the extremes of the highest and lowest values of one index of genetic damage, the frequency of micronucleated erythrocytes in peripheral blood. This index reflects chromosomal damage and loss in bone marrow erythropoietic cells. The assay for micronuclei is convenient but is restricted to splenectomized individuals because the human spleen removes micronucleated cells. The initial 122 subjects were splenectomized, but all were normal and healthy at the time of this study and none had a previous history of neoplastic disease. Factors investigated were stability of micronucleus frequency as a function of time, correlations among multiple markers of genetic damage, and influence on damage indices of nutritional variables, including blood levels of folate, B12 and antioxidant vitamins. Among different individuals, the range of values was 10-fold or more in the erythrocyte micronucleus, glycophorin A, plasma ascorbate and urinary 8-hydroxydeoxyguanosine (oxo8dG) assays, was approximately 6-fold in the lymphocyte micronucleus assay, and was 2-fold in the lymphocyte sister chromatid exchange (SCE) assay. Red blood cell folate and plasma folate, B12 and alpha-tocopherol values varied by up to 10-fold among individuals. Micronucleus frequencies in erythrocytes and peripheral blood lymphocytes ranged from < 0.3 to 16.9/1000 in mature red blood cells, < 1 to 33/1000 in reticulocytes, and 2.5 to 15/1000 in binucleate lymphocytes. Frequencies of glycophorin A variant erythrocytes ranged from 5.6 to 77.3 x 10(6) N/0 cells and 3.2 to 16.2 x 10(6) N/N cells, and oxo8dG excretion varied from 32 to 397 pmol/kg/day. Although a wide range of values was observed in each genetic endpoint, the extreme values for various endpoints of genetic damage were not observed in the same individuals. The frequency of micronucleated erythrocytes varied over time within individuals and indicated that individuals with the highest levels of damage exhibit greater variability than those with lower levels. In some subjects, frequencies of micronucleated erythrocytes changed dramatically over an interval of 2-3 years: four subjects with initial micronucleated reticulocyte frequencies of 20.4, 5.9, 6.4 and 33/1000 changed to 2.5, 20.5, 18.5 and 12/1000, respectively. Among more than 150 individuals we have studied, including the 64 individuals studied by Everson et al. [(1988) J. Natl. Cancer Inst., 80, 525-529] and Smith et al. [(1990) Cancer Res., 50, 5049-5054], the seven individuals with the highest observed frequencies of micronucleated erythrocytes all had exceptionally low values of plasma folate, red cell folate, or plasma B12, suggesting that folate and B12 status are the major determinants of the types of damage that lead to spontaneous micronucleus formation in erythrocytic cells.

摘要

使用多种遗传损伤指标,在22名受试者中研究了遗传损伤的“自发”频率(正常背景)以及这种损伤与人类营养变量之间的可能关系。从最初分析的122名受试者中挑选出这些受试者,原因是他们在外周血微核红细胞频率这一遗传损伤指标上处于最高值和最低值的极端情况。该指标反映了骨髓造血细胞中的染色体损伤和丢失。微核检测很方便,但仅限于脾切除个体,因为人类脾脏会清除微核化细胞。最初的122名受试者均已接受脾切除,但在本研究时他们都正常且健康,且均无肿瘤疾病病史。研究的因素包括微核频率随时间的稳定性、遗传损伤多个标志物之间的相关性以及营养变量对损伤指标的影响,营养变量包括血液中叶酸、维生素B12和抗氧化维生素的水平。在不同个体中,红细胞微核、血型糖蛋白A、血浆抗坏血酸和尿8 - 羟基脱氧鸟苷(oxo8dG)检测的值范围为10倍或更多,淋巴细胞微核检测约为6倍,淋巴细胞姐妹染色单体交换(SCE)检测为2倍。个体间红细胞叶酸、血浆叶酸、维生素B12和α - 生育酚的值变化高达10倍。成熟红细胞中红细胞微核和外周血淋巴细胞微核频率范围为<0.3至16.9/1000,网织红细胞中为<1至33/1000,双核淋巴细胞中为2.5至15/1000。血型糖蛋白A变异红细胞频率范围为5.6至77.3×10⁶ N/0细胞和3.2至16.2×10⁶ N/N细胞,oxo8dG排泄量从32至397 pmol/kg/天不等。尽管在每个遗传终点观察到广泛的值范围,但不同遗传损伤终点的极端值并未在同一受试者中出现。个体红细胞微核频率随时间变化,表明损伤水平最高的个体比损伤水平较低的个体表现出更大的变异性。在一些受试者中,红细胞微核频率在2 - 3年的时间间隔内发生了显著变化:4名初始微核网织红细胞频率分别为20.4、5.9、6.4和33/1000的受试者,分别变为2.5、20.5、18.5和12/1000。在我们研究的150多名受试者中,包括Everson等人[(1988年)《国家癌症研究所杂志》,80卷,525 - 529页]和Smith等人[(1990年)《癌症研究》,50卷,5049 - 5054页]研究的64名受试者,观察到红细胞微核频率最高的7名受试者血浆叶酸、红细胞叶酸或血浆维生素B12的值都异常低,这表明叶酸和维生素B12状态是导致红细胞中自发形成微核的损伤类型的主要决定因素。

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