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源自T细胞受体或重组激活基因1与p53双突变小鼠的未成熟胸腺细胞系的特性分析

Characterization of immature thymocyte lines derived from T-cell receptor or recombination activating gene 1 and p53 double mutant mice.

作者信息

Mombaerts P, Terhorst C, Jacks T, Tonegawa S, Sancho J

机构信息

Howard Hughes Medical Institute, Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Aug 1;92(16):7420-4. doi: 10.1073/pnas.92.16.7420.

Abstract

The T-cell receptor (TCR) beta chain is instrumental in the progression of thymocyte differentiation from the CD4-CD8- to the CD4+CD8+ stage. This differentiation step may involve cell surface expression of novel CD3-TCR complexes. To facilitate biochemical characterization of these complexes, we established cell lines from thymic lymphomas originating from mice carrying a mutation in the p53 gene on the one hand and a mutation in TCR-alpha, TCR-beta, or the recombination activating gene 1 (RAG-1) on the other hand. The cell lines were CD4+CD8+ and appeared to be monoclonal. A cell line derived from a RAG-1 x p53 double mutant thymic lymphoma expressed low levels of CD3-epsilon, -gamma, and -delta on the surface. TCR-alpha x p53 double mutant cell lines were found to express complexes consisting of TCR-beta chains associated with CD3-epsilon, -gamma, and -delta chains and CD3-zeta zeta dimers. These lines will be useful tools to study the molecular structure and signal transducing properties of partial CD3-TCR complexes expressed on the surface of immature thymocytes.

摘要

T细胞受体(TCR)β链在胸腺细胞从CD4⁻CD8⁻阶段向CD4⁺CD8⁺阶段分化的过程中发挥着重要作用。这一分化步骤可能涉及新型CD3 - TCR复合物的细胞表面表达。为了便于对这些复合物进行生化特性分析,我们建立了细胞系,这些细胞系一方面源自携带p53基因突变的小鼠的胸腺淋巴瘤,另一方面源自TCR - α、TCR - β或重组激活基因1(RAG - 1)发生突变的小鼠的胸腺淋巴瘤。这些细胞系为CD4⁺CD8⁺,且似乎是单克隆的。源自RAG - 1 x p53双突变胸腺淋巴瘤的细胞系在表面表达低水平的CD3 - ε、-γ和-δ。发现TCR - α x p53双突变细胞系表达由与CD3 - ε、-γ和-δ链以及CD3 - ζζ二聚体相关的TCR - β链组成的复合物。这些细胞系将成为研究未成熟胸腺细胞表面表达的部分CD3 - TCR复合物的分子结构和信号转导特性的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a24/41351/ed7dc6fd1b6d/pnas01494-0295-a.jpg

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