Crapper R M, Schrader J W
Immunology. 1986 Apr;57(4):553-8.
The T-cell lymphokine, persisting-cell stimulating factor (PSF or interleukin-3), was detected in the serum of mice undergoing graft-versus-host reactions (GVHR). Gel filtration under non-dissociating conditions indicated that the PSF in the serum had an apparent molecular weight of 34,000, a figure identical with that of PSF generated from activated T cells in vitro, indicating that PSF was not bound by serum proteins. The GVHR was accompanied by increases in the numbers in the bone marrow and spleen of precursors of PSF-dependent mast cells, and increases in the numbers of mast cells, megakaryocytes and immature and mature neutrophils in the spleen. These effects of GVHR on haemopoietic cells paralleled those seen when haemopoietic tissues were stimulated with pure PSF in vitro and closely resembled those induced in previous studies by the presence of a tumour that secreted PSF alone. These studies are the first to show that PSF can enter the circulation during immune reactions in vivo and suggest that much of the stimulation of haemopoietic cells seen in GVHR, can be accounted for by the release of PSF from activated T cells.
在发生移植物抗宿主反应(GVHR)的小鼠血清中检测到了T细胞淋巴因子——持久细胞刺激因子(PSF或白细胞介素-3)。在非解离条件下进行的凝胶过滤表明,血清中的PSF表观分子量为34,000,这一数值与体外活化T细胞产生的PSF相同,表明PSF未与血清蛋白结合。GVHR伴随着PSF依赖性肥大细胞前体细胞在骨髓和脾脏中的数量增加,以及脾脏中肥大细胞、巨核细胞和未成熟及成熟中性粒细胞数量的增加。GVHR对造血细胞的这些影响与体外使用纯PSF刺激造血组织时观察到的影响相似,并且与先前研究中仅由分泌PSF的肿瘤所诱导的影响极为相似。这些研究首次表明,PSF能够在体内免疫反应期间进入循环系统,并提示在GVHR中所见到的对造血细胞的大部分刺激作用,可由活化T细胞释放PSF来解释。