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T细胞重排基因γ:T细胞急性淋巴细胞白血病新鲜细胞中的多样性及mRNA表达

T cell rearranging gene gamma: diversity and mRNA expression in fresh cells from T cell acute lymphoblastic leukemia.

作者信息

Le Paslier D, Chen Z, Loiseau P, Cohen D, Sigaux F

出版信息

Blood. 1987 Sep;70(3):637-46.

PMID:3497677
Abstract

Rearrangement and in most cases expression of the T cell rearranging genes gamma (TRG gamma) and T cell antigen receptor beta chain (TCR beta) genes were studied in 19 cases of T cell acute malignancies where the surface phenotype is representative of the different stages of thymic maturation. TCR alpha gene transcription was also studied. TRG gamma and TCR beta genes were found to be rearranged in all but one case. The TRG gamma rearrangement pattern seen in most cases is compatible with biallelic rearrangement by loop excision involving the J gamma 2 regions. The sizes of all but two rearranged bands were identical to those of the rearranged bands seen in polyclonal T lymphocytes also studied in this work. One identical-sized band was found in 11 of the 18 rearranged cases. The expression of TRG gamma mRNA (transcripts of 1.6 kilobases [kb]) was highly variable from case to case and did not correlate with the stage of differentiation of the malignant cells, the expression of the molecules CD4 and CD8, the expression and size of the transcripts of the TCR beta genes, and the transcription of TCR alpha genes. In one CD3 + case, strong expression of the TRG gamma transcripts coexisted with the exclusive presence of TCR beta mRNA of 1.0 kb. The cells from this case did not react with anti-Ti antibody and exhibited no natural killer activity. These findings are suggestive of a malignancy that may express the recently isolated CD3-TRG gamma complex.

摘要

在19例T细胞急性恶性肿瘤中研究了T细胞重排基因γ(TRGγ)和T细胞抗原受体β链(TCRβ)基因的重排情况,多数情况下还研究了其表达情况,这些病例的表面表型代表胸腺成熟的不同阶段。还研究了TCRα基因转录情况。发现除1例之外,其余所有病例中TRGγ和TCRβ基因均发生了重排。多数情况下观察到的TRGγ重排模式与通过涉及Jγ2区域的环切除进行的双等位基因重排相符。除两条重排带外,其余所有重排带的大小均与本研究中同时检测的多克隆T淋巴细胞中的重排带大小相同。在18例重排病例中的11例中发现了一条大小相同的带。TRGγ mRNA(1.6千碱基[kb]的转录本)的表达在不同病例间差异很大,且与恶性细胞的分化阶段、分子CD4和CD8的表达、TCRβ基因转录本的表达及大小以及TCRα基因的转录均无相关性。在1例CD3 +病例中,TRGγ转录本的强表达与仅存在1.0 kb的TCRβ mRNA同时存在。该病例的细胞不与抗Ti抗体反应,也不表现出自然杀伤活性。这些发现提示可能存在一种可表达最近分离出的CD3 - TRGγ复合物的恶性肿瘤。

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