Grabstein K H, Waldschmidt T J, Finkelman F D, Hess B W, Alpert A R, Boiani N E, Namen A E, Morrissey P J
Immunex Research and Development Corporation, Seattle, Washington 98101.
J Exp Med. 1993 Jul 1;178(1):257-64. doi: 10.1084/jem.178.1.257.
The effects of interleukin 7 (IL-7) on the growth and differentiation of murine B cell progenitors has been well characterized using in vitro culture methods. We have investigated the role of IL-7 in vivo using a monoclonal antibody that neutralizes IL-7. We find that treatment of mice with this antibody completely inhibits the development of B cell progenitors from the pro-B cell stage forward. We also provide evidence that all peripheral B cells, including those of the B-1 and conventional lineages, are derived from IL-7-dependent precursors. The results are consistent with the rapid turnover of B cell progenitors in the marrow, but a slow turnover of mature B cells in the periphery. In addition to effects on B cell development, anti-IL-7 treatment substantially reduced thymus cellularity, affecting all major thymic subpopulations.
白细胞介素7(IL-7)对小鼠B细胞祖细胞生长和分化的影响已通过体外培养方法得到充分表征。我们使用一种中和IL-7的单克隆抗体在体内研究了IL-7的作用。我们发现用这种抗体处理小鼠会完全抑制从前B细胞阶段开始的B细胞祖细胞的发育。我们还提供证据表明,所有外周B细胞,包括B-1和传统谱系的B细胞,均源自依赖IL-7的前体细胞。这些结果与骨髓中B细胞祖细胞的快速更新一致,但与外周成熟B细胞的缓慢更新一致。除了对B细胞发育的影响外,抗IL-7处理还显著降低了胸腺细胞数量,影响了所有主要的胸腺亚群。