Matsuzaki Y, Gyotoku J, Ogawa M, Nishikawa S, Katsura Y, Gachelin G, Nakauchi H
Laboratory of Cell Growth and Differentiation, Institute of Physical and Chemical Research (RIKEN), Tsukuba, Japan.
J Exp Med. 1993 Oct 1;178(4):1283-92. doi: 10.1084/jem.178.4.1283.
We found that c-kit-positive, lineage marker-negative, Thy-1lo cells are present in both bone marrow and thymus ("BM c-kit" and "thymus c-kit" cells). Although the two cell types are phenotypically similar, only BM c-kit cells showed the potential to form colonies in vitro as well as in vivo. However, both of them revealed extensive growth and differentiation potential to T cells after direct transfer into an irradiated adult thymus, or a deoxyguanosine-treated fetal thymus. Time course analysis showed that thymus c-kit cells differentiated into CD4CD8 double-positive cells approximately 4 d earlier than BM c-kit cells did. In addition, anti-c-kit antibody blocked T cell generation of BM c-kit cells but not of thymus c-kit cells. Intravenous injection of thymus c-kit resulted in the generation of not only T cells, but B as well as NK1.1+ cells. These data provide evidence that thymus c-kit cells represent common lymphoid progenitors with the differentiation potential to T, B, and possibly NK cells. The c-kit-mediated signaling appears to be essential in the transition from BM c-kit to thymus c-kit cells.
我们发现,c-kit阳性、谱系标志物阴性、Thy-1lo细胞存在于骨髓和胸腺中(“骨髓c-kit”和“胸腺c-kit”细胞)。尽管这两种细胞类型在表型上相似,但只有骨髓c-kit细胞在体外和体内均显示出形成集落的潜力。然而,将它们直接移植到受辐照的成年胸腺或经脱氧鸟苷处理的胎儿胸腺后,二者均显示出向T细胞广泛的生长和分化潜力。时间进程分析表明,胸腺c-kit细胞分化为CD4CD8双阳性细胞的时间比骨髓c-kit细胞早约4天。此外,抗c-kit抗体可阻断骨髓c-kit细胞而非胸腺c-kit细胞的T细胞生成。静脉注射胸腺c-kit不仅导致T细胞生成,还导致B细胞以及NK1.1+细胞生成。这些数据证明胸腺c-kit细胞代表具有向T、B以及可能向NK细胞分化潜力的常见淋巴样祖细胞。c-kit介导的信号传导似乎在从骨髓c-kit细胞向胸腺c-kit细胞的转变中至关重要。