Hosono M, Fujiwara M, Katsura Y
Mech Ageing Dev. 1984 Feb;24(2):197-210. doi: 10.1016/0047-6374(84)90071-x.
When young (6-week-old) BALB/c and also young C57BL/6 mice were inoculated into footpads with spleen cells from normal, syngeneic, aged donors, their response to the inoculum resulted in the enlargement of popliteal lymph nodes (PLN). The degree of PLN enlargement increased as the age of donor mice increased up to age one year. Spleen and lymph node cell populations were highly effective in eliciting the PLN enlargement. Thymus cells and bone marrow cells were moderately effective, but erythrocytes were ineffective. Resident peritoneal exudate cells and spleen adherent cells were much more effective than a whole spleen cell population. The syngeneic response seems to be attributable to a host-versus-graft reaction, since the PLN response was not affected by 2000 rad irradiation of inoculum cells and since the nylon wool-passed spleen T cell population was ineffective as the stimulator. The response was significantly reduced 3 weeks after thymectomy of recipients. PLN enlargement was also observed in older (7-month-old) mice which received spleen cells of younger mice. In this case, however, the response is ascribable to a graft-versus-host reaction, since the inoculation of radiosensitive spleen T cells into footpads resulted in the PLN enlargement. On the other hand, such a stimulatory activity was not found in either lymph node cells or thymus cells. These results suggest that the antigenicity of adherent cells changes with age and that the change is discernible by spleen-locating and short-lived T cells of young mice.
当将来自同基因正常老龄供体的脾细胞接种到年幼(6周龄)的BALB/c小鼠以及年幼的C57BL/6小鼠的足垫中时,它们对接种物的反应导致腘窝淋巴结(PLN)肿大。随着供体小鼠年龄增长至1岁,PLN肿大程度增加。脾细胞和淋巴结细胞群体在引发PLN肿大方面非常有效。胸腺细胞和骨髓细胞效果中等,但红细胞无效。驻留腹膜渗出细胞和脾黏附细胞比整个脾细胞群体更有效。同基因反应似乎归因于宿主抗移植物反应,因为接种细胞经2000拉德照射后PLN反应不受影响,且尼龙毛柱通过的脾T细胞群体作为刺激物无效。受体胸腺切除3周后反应显著降低。在接受年幼小鼠脾细胞的老龄(7月龄)小鼠中也观察到PLN肿大。然而,在这种情况下,反应归因于移植物抗宿主反应,因为将放射敏感的脾T细胞接种到足垫中会导致PLN肿大。另一方面,在淋巴结细胞或胸腺细胞中均未发现这种刺激活性。这些结果表明黏附细胞的抗原性随年龄变化,且这种变化可被年幼小鼠的脾定位且寿命短暂的T细胞识别。