Dumont F, Habbersett R C
Clin Exp Immunol. 1982 Jul;49(1):87-95.
The composition of the thymocyte population was investigated as a function of age in the autoimmunity-prone NZB x NZW F1 (NZB x W) female mice and in control BALB/c female mice. Single- and two-colour flow cytofluorometry analyses were used to quantitate the cell surface binding of fluorochrome-conjugated antibodies directed against various lymphocyte markers and of fluoresceinated peanut agglutinin (PNA). In both mouse strains, two major phenotypically distinct thymocyte subpopulations were thus identified. The predominant subpopulation was characterized as bright Thy-1+, Lyt-1 + 2+ and bright PNA+, and the other one as dull Thy-1+, Lyt-1 + 2- and dull PNA+. The relative frequencies of these two subpopulations were similar in NZB x W and BALB/c mice at 3 months of age. However, from 6 months onwards, slight but significant differences became detectable between the two strains. Thus, in BALB/c mice, both thymocyte subpopulations regressed at approximately the same rate during ageing so that their relative proportions remained constant. In contrast, in NZB x W mice, while the number of bright Thy-1+ cells diminished as in BALB/c mice, the number of dull Thy-1+ cells barely varied from 3 to 12 months of age, which resulted in a proportional increase of this latter subpopulation. Moreover, elevated frequencies of surface immunoglobulin-bearing cells were recorded in the thymus of 8-12 month old NZB x W mice but not in BALB/c mice. Therefore, the development of autoimmunity in NZB x W mice appears associated with an abnormal age-dependent evolution of the intrathymic lymphocyte population.
在易患自身免疫性疾病的NZB×NZW F1(NZB×W)雌性小鼠和对照BALB/c雌性小鼠中,研究了胸腺细胞群体组成随年龄的变化。采用单染色和双染色流式细胞荧光术分析,以定量针对各种淋巴细胞标志物的荧光染料偶联抗体和荧光素化花生凝集素(PNA)的细胞表面结合情况。在这两种小鼠品系中,由此鉴定出两个主要的表型不同的胸腺细胞亚群。占主导地位的亚群特征为Thy-1+明亮、Lyt-1 + 2+明亮且PNA+明亮,另一个亚群特征为Thy-1+暗淡、Lyt-1 + 2-暗淡且PNA+暗淡。这两个亚群的相对频率在3月龄的NZB×W和BALB/c小鼠中相似。然而,从6月龄起,两个品系之间出现了轻微但显著的差异。因此,在BALB/c小鼠中,两个胸腺细胞亚群在衰老过程中以大致相同的速率消退,因此它们的相对比例保持恒定。相比之下,在NZB×W小鼠中,虽然明亮的Thy-1+细胞数量如在BALB/c小鼠中一样减少,但暗淡的Thy-1+细胞数量在3至12月龄之间几乎没有变化,这导致后一个亚群的比例增加。此外,在8至12月龄的NZB×W小鼠胸腺中记录到表面免疫球蛋白阳性细胞的频率升高,而在BALB/c小鼠中未记录到。因此,NZB×W小鼠自身免疫性疾病的发展似乎与胸腺内淋巴细胞群体异常的年龄依赖性演变有关。