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通过逆转录病毒转导小鼠原代 CD4 T 细胞对 Foxp3 及其突变体的功能分析。

Functional Analysis of Foxp3 and Its Mutants by Retroviral Transduction of Murine Primary CD4 T Cells.

机构信息

Laboratory of Immunology and Microbiology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.

出版信息

Methods Mol Biol. 2023;2559:79-94. doi: 10.1007/978-1-0716-2647-4_7.

Abstract

The transcription factor Foxp3/FOXP3 orchestrates regulatory T (Treg) cell development and function by interacting with numerous target genes and partner proteins. Functional analysis of naturally occurring or engineered Foxp3/FOXP3 mutations has provided important insights into how the complex Foxp3/FOXP3-centered molecular network operates. Here, we describe detailed protocols for retroviral transduction of murine primary conventional CD4 T cells to determine the impacts of Foxp3 mutations on the Treg-cell-like phenotype and function conferred by Foxp3.

摘要

转录因子 Foxp3/FOXP3 通过与众多靶基因和伙伴蛋白相互作用来协调调节性 T(Treg)细胞的发育和功能。对天然或工程 Foxp3/FOXP3 突变的功能分析为了解复杂的 Foxp3/FOXP3 为中心的分子网络如何运作提供了重要的见解。在这里,我们描述了用逆转录病毒转导小鼠原代常规 CD4 T 细胞的详细方案,以确定 Foxp3 突变对 Foxp3 赋予的 Treg 样表型和功能的影响。

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