QUANTITATIVE REPRESENTATION OF ALL T-CELLS COMMITTED TO DEVELOP INTO CYTO-TOXIC EFFECTOR-CELLS AND OR INTERLEUKIN-2 ACTIVITY-PRODUCING HELPER-CELLS WITHIN MURINE LYMPHOCYTE-T SUBSETS

QUANTITATIVE REPRESENTATION OF ALL T-CELLS COMMITTED TO DEVELOP INTO CYTO-TOXIC EFFECTOR-CELLS AND OR INTERLEUKIN-2 ACTIVITY-PRODUCING HELPER-CELLS WITHIN MURINE LYMPHOCYTE-T SUBSETS
复制标题

DOI:
10.1002/eji.1830140107
复制
发表时间:
1984-01-01
影响因子:
5.4
通讯作者:
WAGNER, H
WAGNER, H
中科院分区:
医学3区
文献类型:
--
作者:
PFIZENMAIER, K;SCHEURICH, P;WAGNER, H

文献摘要

被引文献

相似文献

以豆豆蛋白A (cona)刺激为基础的限制性稀释培养系统,研究了lyt -2定义的小鼠T细胞亚群中辅助细胞和细胞毒性前体细胞的定量分布。几乎所有选择的Lyt-2+和lyt - T细胞在8至9天的培养期内生长并扩增成大型克隆菌落。经Con A刺激后,90%的Lyt-2- T细胞能够产生白细胞介素2 (IL -2)活性。8-10%的Lyt-2+ T细胞产生IL2活性。在克隆水平上,Lyt-2+ T细胞产生的IL -2活性的平均值为。与Lyt-2- T细胞相比减少了8倍。细胞毒性T细胞的前体几乎只存在于Lyt-2+群体中,其中。70%的小鼠在凝集素依赖性细胞溶解试验中显示裂解活性。对于绝大多数被分析的克隆,产生IL - 2活性的能力和表达裂解活性的能力是相互排斥的。少数克隆(< 3%)同时产生IL - 2活性并表达细胞毒性。因此,后一种细胞被认为是双功能T细胞。
A limiting dilution culture system based on stimulation with concanavalin A (Con A) was used to study the quantitative distribution of helper and of cytotoxic precursor cells in a Lyt-2-defined subpopulation of murine T cells. Virtually all of the selected Lyt-2+ and Lyt-2- T cells grow and expand to large clonal colonies within an 8 to 9 day culture period. Upon stimulation with Con A, 90% of the Lyt-2- T cells were capable of producing interleukin 2 (IL 2) activity. IL2 activity is produced by 8-10% of Lyt-2+ T cells. At the clonal level, the average of the IL 2 activity produced by Lyt-2+ T cells is .apprx. 8-fold less as compared to Lyt-2- T cells. Precursors of cytotoxic T cells were almost exclusively found in the Lyt-2+ population, of which .apprx. 70% displayed lytic activity in a lectin-dependent cytolysis test. For the vast majority of clones analyzed, the capacity to produce IL 2 activity and the capacity to express lytic activity was mutually exclusive. A minority of clones (< 3%) simultaneously produced IL 2 activity and expressed cytotoxicity. These latter cells are therefore considered as bifunctional T cells.