Vanhecke D, Verhasselt B, Debacker V, Leclercq G, Plum J, Vandekerckhove B
Department of Clinical Chemistry, Microbiology and Immunology, University Hospital, Ghent, Belgium.
J Immunol. 1995 Nov 15;155(10):4711-8.
We investigated at which point during thymocyte differentiation functions were acquired that are characteristic for mature Th cells. Differentiation from CD3+CD69-, CD4+CD8+ double-positive (DP) cells to terminally differentiated CD3+, CD4+CD8- single-positive (SP) cells was broken down into six discrete stages that were purified by four-color sorting: CD69-CD3+DP (stage 0), CD69+CD27-DP (stage 1), CD69+CD27-CD4+SP (stage 2), CD27+CD1+CD4+SP (stage 3), CD1-CD45RO+CD4+SP (stage 4), and CD1-CD45RO-CD4+SP cells (stage 5). Phenotypically, these stages seem to describe consecutive steps in differentiation from immature stage 0 to the terminally matured stage 5. Functionally, the capacity to proliferate on IL-2 after stimulation was absent in CD69- stage 0 cells, but was acquired gradually during stages 1 to 4. Clonal expandability and the capacity to respond to stimulation with the production of cytokines were acquired later and rather abruptly by CD1- stage 4 and 5 cells. Activation markers such as CD69 expression and in vivo IL-2 gene transcription came up simultaneously at the DP stage and peaked at stage 3 to 4. These data suggest that functional maturation of Th cells occurs over an extended period in differentiation, stages 1 to 4, and coincides with a gradual increase in activation markers. After completion of functional differentiation, at stage 5, in vivo IL-2 mRNA transcription and CD69 expression are down-regulated, and the cells become functionally resting naive T cells expressing CD45RA+.
我们研究了胸腺细胞分化过程中在哪个阶段获得了成熟Th细胞所特有的功能。从CD3 + CD69 - 、CD4 + CD8 + 双阳性(DP)细胞分化为终末分化的CD3 + 、CD4 + CD8 - 单阳性(SP)细胞被细分为六个离散阶段,通过四色分选进行纯化:CD69 - CD3 + DP(阶段0)、CD69 + CD27 - DP(阶段1)、CD69 + CD27 - CD4 + SP(阶段2)、CD27 + CD1 + CD4 + SP(阶段3)、CD1 - CD45RO + CD4 + SP(阶段4)和CD1 - CD45RO - CD4 + SP细胞(阶段5)。从表型上看,这些阶段似乎描述了从未成熟的阶段0到终末成熟的阶段5的连续分化步骤。在功能上,阶段0的CD69 - 细胞在受到刺激后缺乏在IL - 2上增殖的能力,但在阶段1至4期间逐渐获得。克隆扩展性以及用细胞因子产生来响应刺激的能力在阶段4和5的CD1 - 细胞中较晚且相当突然地获得。诸如CD69表达和体内IL - 2基因转录等激活标志物在DP阶段同时出现,并在阶段3至4达到峰值。这些数据表明,Th细胞的功能成熟在分化的阶段1至4的较长时期内发生,并且与激活标志物的逐渐增加相一致。在功能分化完成后,在阶段5,体内IL - 2 mRNA转录和CD69表达下调,细胞成为表达CD45RA + 的功能静止的初始T细胞。