Wonigeit K
Klinik Für Abdominal- Und Transplantationschirurgie, Medizinische Hochschule Hannover, Germany.
Adv Exp Med Biol. 1997;419:257-64. doi: 10.1007/978-1-4419-8632-0_33.
The gene products of the RT6 system have been demonstrated to be expressed on the majority of resting peripheral T cells but not on fully activated cytotoxic T cells and in vitro generated long term T cell lines. This has lead to the conclusion that T cell activation causes a loss of RT6 expression. In the present study this question was examined by analysing the expression of RT6 on T cell populations activated in vitro by the T cell mitogen ConA or by allogeneic stimulator cells and subsequently maintained in culture for several weeks. The results showed an initial increase in RT6 expression on most cells during the first two days of culture and a subsequent loss of RT6 expression in many activated cells. Substantial numbers of both CD4+ and CD8+ T cells, however, remained clearly RT6 positive. These cells were present during the entire observation period. The RT6 positive cells did not represent persisting unstimulated cells since they coexpressed CD25 and exhibited typical blast morphology. It is concluded that activation of T cells leads to loss of RT6 expression only in subsets of the CD4 and CD8 T cell populations. The previously reported finding that long term cultures contain only RT6 negative blast cells may indicate preferential survival of RT6 negative blasts rather than obligatory loss of RT6 expression after activation. The possibility is discussed that activated RT6-CD4+ T cells may be inflammatory Th1 cells and activated RT6+CD4+ T lymphoblasts may represent regulatory Th2 cells.
RT6系统的基因产物已被证明在大多数静止外周T细胞上表达,但在完全活化的细胞毒性T细胞和体外产生的长期T细胞系上不表达。由此得出结论,T细胞活化会导致RT6表达丧失。在本研究中,通过分析经T细胞丝裂原刀豆蛋白A或同种异体刺激细胞体外活化并随后在培养中维持数周的T细胞群体上RT6的表达来研究这个问题。结果显示,在培养的前两天,大多数细胞上的RT6表达最初增加,随后许多活化细胞中的RT6表达丧失。然而,大量的CD4+和CD8+ T细胞仍然明显呈RT6阳性。这些细胞在整个观察期内都存在。RT6阳性细胞并不代表持续未受刺激的细胞,因为它们共表达CD25并呈现典型的母细胞形态。得出的结论是,T细胞活化仅导致CD4和CD8 T细胞群体亚群中RT6表达丧失。先前报道的长期培养物仅含有RT6阴性母细胞的发现可能表明RT6阴性母细胞的优先存活,而不是活化后RT6表达的必然丧失。讨论了活化的RT6-CD4+ T细胞可能是炎性Th1细胞,而活化的RT6+CD4+ T淋巴母细胞可能代表调节性Th2细胞的可能性。