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辅助细胞对用抗CD3/T细胞抗原受体复合物抗体刺激小鼠T细胞白血病的影响。

Effect of accessory cells on stimulation of murine T-cell leukemia with antibodies to the CD3/T cell antigen receptor complex.

作者信息

Suto R, Udono H, Yamamoto A, Shiku H, Nakayama E

机构信息

Department of Oncology, Nagasaki University School of Medicine.

出版信息

Jpn J Cancer Res. 1993 Apr;84(4):438-44. doi: 10.1111/j.1349-7006.1993.tb00155.x.

Abstract

Stimulation of EL4 and RL male 1 leukemia cells in vitro with immobilized anti-CD3 epsilon monoclonal antibody (mAb) (145-2C11) or anti-TCR beta mAb (H57-597) in the absence of accessory cells induced interleukin-2 (IL-2) production, and caused growth inhibition. The growth inhibition was, however, transient and the tumors started to grow again within 5 days in immobilizing plates treated with antibodies at concentrations of 2.5-100 micrograms/ml. Addition of mitomycin C-treated accessory cells to the culture inhibited IL-2 production and resulted in augmented and persistent growth inhibition. No recovery of tumor growth was observed. Furthermore, DNA from EL4 and RL male 1 leukemia cells stimulated with anti-CD3/TCR mAbs was fragmented even in the absence of accessory cells, but fragmentation was much greater in the presence of accessory cells. Marginal and high expression of the bcl-2 gene were observed in EL4 and RL male 1, respectively, indicating that apoptosis of these leukemias mediated by signalling through the CD3/TCR complex has no direct relationship with expression of the bcl-2 gene.

摘要

在无辅助细胞的情况下,用固定化抗CD3ε单克隆抗体(mAb)(145-2C11)或抗TCRβ mAb(H57-597)体外刺激EL4和RL male 1白血病细胞,可诱导白细胞介素-2(IL-2)产生,并导致生长抑制。然而,生长抑制是短暂的,在用浓度为2.5-100微克/毫升的抗体处理的固定化平板中,肿瘤在5天内又开始生长。向培养物中添加丝裂霉素C处理的辅助细胞可抑制IL-2产生,并导致增强的和持续的生长抑制。未观察到肿瘤生长的恢复。此外,即使在无辅助细胞的情况下,用抗CD3/TCR mAb刺激的EL4和RL male 1白血病细胞的DNA也会发生片段化,但在有辅助细胞的情况下片段化程度要大得多。在EL4和RL male 1中分别观察到bcl-2基因的边缘表达和高表达,这表明通过CD3/TCR复合体信号传导介导的这些白血病的凋亡与bcl-2基因的表达没有直接关系。

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