胸腺细胞中雌激素受体的表达和功能与性别和年龄的关系。

F Kohen, L Abel, A Sharp, Y Amir-Zaltsman, D Sömjen, S Luria, G Mor, A Knyszynski, H Thole, A Globerson
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引用次数: 47

摘要

研究了年轻、中年、老年(分别为2、12、24月龄)雌性和雄性C57BL/6J小鼠胸腺细胞雌激素受体(ER)的表达。从所有年龄组的女性胸腺细胞制备的Western免疫印迹显示存在67-kD蛋白带,这与变性ER的明显MW有关。用单克隆抗ER抗体(克隆13H2)染色的细胞流式细胞术分析显示,ER在所有年龄组的女性和男性中都有表达。体内雌二醇(E2)处理导致雌性小鼠胸腺肌酸激酶(CK)的特异性活性增加,而雄性胸腺细胞仅在双氢睾酮(DHT)处理时才有CK活性增加的反应。数据显示,男性和女性之间的ER表达没有差异,但受体似乎在男性中不起作用。有趣的是,当雌二醇应用于淋巴细胞缺失的胎儿胸腺(FT)外植体和来自年轻和老年女性的骨髓细胞或胸腺细胞的共同培养时,它导致含有年轻细胞的培养细胞增加,而不是含有老年细胞的培养细胞。在这些培养中,发育细胞的CD4/CD8表型比例不受E2处理的影响。这些观察结果为t细胞发育中ER表达和功能与性别和年龄的关系提供了新的见解。
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Estrogen-receptor expression and function in thymocytes in relation to gender and age.

The expression of estrogen receptor (ER) in thymocytes was studied in young, middle-aged, and old (2, 12, and 24 months, respectively) female and male C57BL/6J mice. Western immunoblots prepared from the thymocytes of females of all age groups showed the presence of a 67-kD protein band, which has been associated with the apparent MW of denatured ER. Flow cytometry analysis of cells stained with a monoclonal anti-ER antibody (clone 13H2) disclosed ER expression in both females and males of all age groups. In vivo treatment with estradiol (E2) led to an increase in the specific activity of thymic creatine kinase (CK) in the female mice, whereas the male thymocytes responded with an increase in CK activity only on treatment with dihydrotestosterone (DHT). The data show no differences in ER expression between male and females, but the receptor appears not to be functional in males. Interestingly, when estradiol was applied to co-cultures of lymphoid-depleted fetal thymus (FT) explants and bone-marrow cells, or thymocytes, from young and old females, it resulted in increased cellularity of cultures containing cells of the young, and not those of the old. The proportion of CD4/CD8 phenotypes of the developing cells in these cultures was not affected by E2 treatment. These observations provide a new insight into ER expression and function in T-cell development in relation to gender and age.

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