Gottesman S R, Kristie J A, Walford R L
Immunology. 1981 Nov;44(3):607-16.
Individual young adult, middle-aged, and old C57BL/6J male mice were tested for in vitro generated proliferative and cytotoxic responses to H-2 alloantigens under a variety of sensitization conditions. Proliferation in mixed lymphocyte culture (MLC) had decreased by 14 months of age (middle-aged), whether measured by directly assaying cultures in microtitre plates (micro MLC) or by labelling aliquots taken from large culture tubes (macro MLC). Cytotoxicity did not decline until a later age if sensitization was done in large tubes (macro cell-mediated lympholysis, CML). When cytotoxic activity was assayed by measuring lysis after addition of chromated cells to MLCs in microtitre plates (micro CML), differences were revealed between young and middle-aged animals. However, these conditions were suboptimal for generation of cytotoxicity even in young controls and showed even lower responses in the middle-aged group. It was concluded that proliferation showed an earlier, more severe decline than cytotoxicity with age as the proliferative response had declined by middle-age under all sensitization conditions used. With optimal sensitization conditions, senescent mice (26--30 months) showed a four- to ten-fold decrease in cytotoxicity compared with young adult mice.
对不同年龄段的C57BL/6J雄性小鼠(包括年轻成年小鼠、中年小鼠和老年小鼠)在多种致敏条件下,测试其对H-2同种异体抗原的体外增殖反应和细胞毒性反应。无论通过微量滴定板直接检测培养物(微量混合淋巴细胞培养,micro MLC)还是标记从大培养管中取出的等分试样(宏观混合淋巴细胞培养,macro MLC)来测量,混合淋巴细胞培养(MLC)中的增殖在14月龄(中年)时就已下降。如果在大培养管中进行致敏(宏观细胞介导的淋巴细胞溶解,CML),细胞毒性直到更晚的年龄才下降。当通过在微量滴定板中将铬化细胞加入MLC后测量裂解来检测细胞毒性活性(微量细胞介导的淋巴细胞溶解,micro CML)时,年轻和中年动物之间出现了差异。然而,即使在年轻对照组中,这些条件对于细胞毒性的产生也是次优的,并且在中年组中反应更低。得出的结论是,随着年龄增长,增殖比细胞毒性更早、更严重地下降,因为在所有使用的致敏条件下,中年时增殖反应就已下降。在最佳致敏条件下,衰老小鼠(26 - 30个月)与年轻成年小鼠相比,细胞毒性降低了4至10倍。