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人T细胞受体γδ阳性细胞(TCR1细胞)的静息(白细胞介素-2无反应性)前体通过双信号过程被激活。

Resting (IL-2 non-responsive) precursors of human T cell receptor gamma delta-positive cells (TCR1 cells) are activated by a two signal process.

作者信息

Warren H S

机构信息

Cancer Research Unit, Woden Valley Hospital, ACT, Australia.

出版信息

Immunol Cell Biol. 1989 Apr;67 ( Pt 2):121-6. doi: 10.1038/icb.1989.17.

Abstract

Precursors of T cells expressing the gamma delta-T cell receptor (TCR1 cells) have been identified in a resting (IL-2 non-responsive) subpopulation of human peripheral blood mononuclear cells (PBMC). Activation of the TCR1 precursor cells into proliferating and cytotoxic cells requires two signals, viz. IL-2 and either activated T cells (autologous or allogeneic) or malignant melanoma cells (MM-170). The activation process is inhibited by 0.1 microgram/ml cyclosporine. CD3 expression on TCR1 precursor cells was low, since the precursor cells were not always adequately depleted by OKT3 plus complement. Natural killer cells were generated from the same resting subpopulation of PBMC and by the same set of activation stimuli as were the TCR1 cells, suggesting a common pathway for activation of both cell types.

摘要

表达γδ-T细胞受体的T细胞前体(TCR1细胞)已在人外周血单个核细胞(PBMC)的静息(对IL-2无反应)亚群中被鉴定出来。将TCR1前体细胞激活为增殖性和细胞毒性细胞需要两个信号,即IL-2和活化的T细胞(自体或同种异体)或恶性黑色素瘤细胞(MM-170)。激活过程受到0.1微克/毫升环孢素的抑制。TCR1前体细胞上的CD3表达较低,因为前体细胞并不总是能被OKT3加补体充分清除。自然杀伤细胞与TCR1细胞一样,由PBMC的同一静息亚群并通过同一组激活刺激产生,这表明两种细胞类型的激活有共同途径。

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