Butler M G, Lane J R
Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN 37232.
Mech Ageing Dev. 1989 Jan;47(1):17-24. doi: 10.1016/0047-6374(89)90003-1.
Silver stained nucleolar organizer regions (AgNORs) were studied in phytohemagglutinin (PHA)-stimulated lymphocytes from 55 Caucasian control individuals (34 females with average age of 24 years and age range 19 weeks gestation to 87 years; 21 males with average age of 31 years and age range 29 weeks gestation to 72 years) and 13 individuals (7 females, 6 males; average age 38.8 years with age range 25-58 years) with multiple endocrine neoplasia-type II (MEN-II), an autosomal dominant malignancy with increased chromosome breakage. For the first time, AgNORs were examined in lymphocytes from normal fetuses and patients with MEN-II in order to determine the effects of age, sex or malignancy on the number of AgNORs. No significant difference in the average number of AgNORs were found in fetal cells (8.2 +/- S.D. 0.7/cell) when compared with cells from older individuals including those over 65 years of age (8.0 +/- S.D. 0.8/cell). There was a statistically significant negative correlation (P less than 0.05) between the modal number of AgNORs on G but not D chromosomes in both males and females. A negative correlation was also found between the mean number of AgNORs and age but was not statistically significant. The average number of AgNORs in the MEN-II individuals was 8.5 +/- S.D. 0.7/cell, which was not significantly different than 8.2 +/- S.D. 0.7/cell observed in age-matched control subjects.
对55名高加索对照个体(34名女性,平均年龄24岁,年龄范围从妊娠19周至87岁;21名男性,平均年龄31岁,年龄范围从妊娠29周至72岁)以及13名患有多发性内分泌肿瘤II型(MEN-II)的个体(7名女性,6名男性;平均年龄38.8岁,年龄范围25 - 58岁)的植物血凝素(PHA)刺激淋巴细胞进行了银染核仁组织区(AgNORs)研究。MEN-II是一种常染色体显性恶性肿瘤,其染色体断裂增加。首次对正常胎儿和MEN-II患者的淋巴细胞进行AgNORs检查,以确定年龄、性别或恶性肿瘤对AgNORs数量的影响。与包括65岁以上个体的细胞相比,胎儿细胞中AgNORs的平均数量(8.2±标准差0.7/细胞)未发现显著差异。在男性和女性中,G染色体而非D染色体上AgNORs的众数数量之间存在统计学显著的负相关(P小于0.05)。AgNORs的平均数与年龄之间也发现了负相关,但无统计学意义。MEN-II个体中AgNORs的平均数量为8.5±标准差0.7/细胞,与年龄匹配的对照受试者中观察到的8.2±标准差0.7/细胞无显著差异。