Ulmer A J, Flad H D
Immunobiology. 1982 May;161(5):476-87. doi: 10.1016/S0171-2985(82)80050-8.
Interleukin-2 (Il-2) producing human T-lymphocyte subsets were isolated by discontinuous density gradient centrifugation and their requirements for helper monocytes were investigated. The results show that T-lymphocytes from fractions 2, 3, and 4 from the density gradient (high density lymphocytes) which contain up to 75% Fcmu receptor-bearing cells, and less than 0.2% monocytes could be stimulated by PHA for the production of Il-2 only in the presence of additional monocytes. T-lymphocytes from fractions 6 and 7 and in most experiments also from fraction 5 (low-density lymphocytes containing between 20% and 50% Fcmu receptor bearing cells, but still 0.2% up to 30% monocytes) could be stimulated by PHA for the production of Il-2 also without additional monocytes. Dose-response experiments with various numbers of monocytes added to the system showed the following: the higher the density of a cell population, the higher the number of monocytes required for help in the stimulation of Il-2 production. However, the production of Il-2 by high-density lymphocytes did not reach the Il-2 production by low-density T-lymphocytes even in the presence of high numbers of additional monocytes. Dose-response experiments indicated that the difference in Il-2 producing activity of T-lymphocytes of different density cannot be explained by the various numbers and/or activities of residual monocytes present in the various T-cell fractions. We suggest that the various T-lymphocyte populations differ with respect to a further cell population, presumably of lymphatic origin. This population appears to participate in the regulation of Il-2 production.
通过不连续密度梯度离心法分离出产生白细胞介素-2(Il-2)的人T淋巴细胞亚群,并研究了它们对辅助单核细胞的需求。结果表明,密度梯度中第2、3和4组分(高密度淋巴细胞)中的T淋巴细胞,其中含有高达75%携带Fcmu受体的细胞,且单核细胞少于0.2%,只有在存在额外单核细胞的情况下,才能被PHA刺激产生Il-2。来自第6和7组分的T淋巴细胞,以及在大多数实验中来自第5组分(低密度淋巴细胞,含有20%至50%携带Fcmu受体的细胞,但仍有0.2%至30%的单核细胞)的T淋巴细胞,也可以在没有额外单核细胞的情况下被PHA刺激产生Il-2。向系统中添加不同数量单核细胞的剂量反应实验表明:细胞群体的密度越高,刺激Il-2产生所需的辅助单核细胞数量就越高。然而,即使存在大量额外的单核细胞,高密度淋巴细胞产生的Il-2也未达到低密度T淋巴细胞产生的Il-2水平。剂量反应实验表明,不同密度的T淋巴细胞产生Il-2活性的差异不能用不同T细胞组分中存在的残余单核细胞的数量和/或活性来解释。我们认为,不同的T淋巴细胞群体在另一种细胞群体方面存在差异,推测该群体起源于淋巴系统。该群体似乎参与了Il-2产生的调节。