Kong Yuelin, Jing Yi, Bettini Maria
Department of Pediatrics, Section of Diabetes and Endocrinology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas.
McNair Medical Institute, Houston, Texas.
Curr Protoc Immunol. 2019 Jun;125(1):e76. doi: 10.1002/cpim.76. Epub 2019 May 15.
The ability to express and study a single T cell receptor (TCR) in vivo is an important aspect of both basic and translational immunological research. Traditionally, this was achieved by using TCR transgenic mice. In the past decade, a more efficient approach for single TCR expression was developed. This relatively rapid and accessible method utilizes retrovirus-mediated stem cell-based gene transfer and is commonly referred to as the TCR retrogenic approach. In this approach, hematopoietic bone marrow precursors are transduced with retroviral vector carrying both alpha and beta chains of a T cell receptor. After successful transduction, bone marrow is injected into recipient mice, in which T cell development is driven by expression of the vector-encoded TCR. This article details the materials and methods required to generate TCR retrogenic mice. It is divided into three sections and provides detailed methods for generation of stable retroviral producer cell lines, isolation and optimal transduction of hematopoietic bone marrow cells, and subsequent analysis of TCR retrogenic T cells. A detailed example of such analysis is provided. The current protocol is a culmination of many years of optimization and is the most efficient approach to date. Bone marrow transduction and transfer into recipient mice can now be achieved in a short period of four days. The protocol can be followed in most laboratories with standard biomedical equipment, and is supported by a troubleshooting guide that covers potential pitfalls and unexpected results. © 2019 by John Wiley & Sons, Inc.
在体内表达和研究单一T细胞受体(TCR)的能力是基础免疫学研究和转化免疫学研究的一个重要方面。传统上,这是通过使用TCR转基因小鼠来实现的。在过去十年中,开发了一种更有效的单一TCR表达方法。这种相对快速且易于操作的方法利用逆转录病毒介导的基于干细胞的基因转移,通常被称为TCR逆转基因方法。在这种方法中,造血骨髓前体细胞用携带T细胞受体α链和β链的逆转录病毒载体进行转导。成功转导后,将骨髓注射到受体小鼠体内,在受体小鼠中,载体编码的TCR的表达驱动T细胞发育。本文详细介绍了生成TCR逆转基因小鼠所需的材料和方法。它分为三个部分,提供了生成稳定逆转录病毒生产细胞系、分离和优化转导造血骨髓细胞以及随后分析TCR逆转基因T细胞的详细方法。提供了这种分析的详细示例。当前的方案是多年优化的成果,是迄今为止最有效的方法。现在可以在短短四天内完成骨髓转导并将其转移到受体小鼠体内。大多数实验室使用标准生物医学设备即可遵循该方案,并且有一个故障排除指南作为支持,该指南涵盖了潜在的陷阱和意外结果。© 2019约翰威立父子公司。