Viale A C, Chies J A, Huetz F, Malenchere E, Weksler M, Freitas A A, Coutinho A
Unité d'Immunobiologie, Institut Pasteur, Paris, France.
Scand J Immunol. 1994 Feb;39(2):184-8. doi: 10.1111/j.1365-3083.1994.tb03358.x.
The cellular composition and VH-gene family repertoire were compared in different B-cell compartments from young adult (8-12 weeks) and old (18-24 months) C57BL/6 and BALB/c mice. Ageing mice were found to have a higher frequency of peripheral mature B cells utilizing genes from a single VH-gene family. While in each individual old C57BL/6 mice cells expressing the VH J558 gene family consistently were over-represented, a marked individual variation was observed in old BALB/c mice with increased frequency of either the VH J558, Q52 or J606 families. Aged mice were found also to have a reduced number of bone-marrow pre-B cells and an augmented number of splenic Ig-secreting cells. These results suggest that old mice express less diversified antibody repertoires possibly as a consequence of reduced input from precursors and increased peripheral selection, which may be responsible for the progressive establishment of immunodeficiency.
比较了年轻成年(8 - 12周)和老年(18 - 24个月)C57BL/6和BALB/c小鼠不同B细胞区室的细胞组成和VH基因家族库。发现衰老小鼠利用单个VH基因家族基因的外周成熟B细胞频率更高。虽然在每只老年C57BL/6小鼠中,表达VH J558基因家族的细胞始终占优势,但在老年BALB/c小鼠中观察到明显的个体差异,VH J558、Q52或J606家族的频率增加。还发现老年小鼠骨髓前B细胞数量减少,脾脏Ig分泌细胞数量增加。这些结果表明,老年小鼠表达的抗体库多样性较低,这可能是由于前体细胞输入减少和外周选择增加所致,这可能是免疫缺陷逐渐形成的原因。