Egerton M, Scollay R, Shortman K
Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Proc Natl Acad Sci U S A. 1990 Apr;87(7):2579-82. doi: 10.1073/pnas.87.7.2579.
We have reexamined the balance between cell birth, cell maturation, and cell death in the thymus by labeling dividing thymocytes and their progeny in vivo with [3H]-thymidine, isolating clearly defined subpopulations by fluorescence-activated cell sorting, and determining the distribution of label by autoradiography. When mature thymocytes were precisely defined (as CD4+CD8- CD3+ or CD4-CD8+ CD3+) and separated from immature single positives (CD4+CD8- CD3- and CD4-CD8+ CD3-), a lag was observed in the rate of entry of [3H]thymidine into mature cells. Thus, many of the mature thymocytes appear to derive from a small nondividing cortical thymocyte pool, rather than originating directly from the earliest dividing CD4+CD8+ blasts. There was little evidence for cell division during or after mature thymocyte formation, suggesting a one-for-one differentiation from cortical cells rather than selective clonal expansion. The rate of production of mature single positive thymocytes agreed closely with estimates of the rate of export of mature T cells from the thymus and was only 3% of the rate of production of double-positive cortical thymocytes. This was compatible with a stringent selection process and extensive intrathymic cell death and suggested that no extensive negative selection occurred after the mature cells were formed.
我们通过在体内用[3H] - 胸腺嘧啶核苷标记正在分裂的胸腺细胞及其子代,利用荧光激活细胞分选技术分离出明确界定的亚群,并通过放射自显影确定标记的分布,重新审视了胸腺中细胞生成、细胞成熟和细胞死亡之间的平衡。当将成熟胸腺细胞精确界定为(CD4 + CD8 - CD3 +或CD4 - CD8 + CD3 +)并与未成熟单阳性细胞(CD4 + CD8 - CD3 - 和CD4 - CD8 + CD3 -)分离时,观察到[3H]胸腺嘧啶核苷进入成熟细胞的速率存在滞后现象。因此,许多成熟胸腺细胞似乎源自一个不分裂的小皮质胸腺细胞池,而非直接起源于最早分裂的CD4 + CD8 +母细胞。在成熟胸腺细胞形成期间或之后几乎没有细胞分裂的证据,这表明是从皮质细胞一对一分化而来,而非选择性克隆扩增。成熟单阳性胸腺细胞的产生速率与从胸腺输出成熟T细胞的速率估计值密切相符,且仅为双阳性皮质胸腺细胞产生速率的3%。这与严格的选择过程和广泛的胸腺内细胞死亡相一致,并表明成熟细胞形成后未发生广泛的阴性选择。