Uematsu Y, Ryser S, Dembić Z, Borgulya P, Krimpenfort P, Berns A, von Boehmer H, Steinmetz M
Basel Institute for Immunology, Switzerland.
Cell. 1988 Mar 25;52(6):831-41. doi: 10.1016/0092-8674(88)90425-4.
Transgenic mice were constructed with a functional T cell receptor beta gene. Transcription of the introduced gene is largely confined to T cells, but low levels of transcripts are also seen in B cells and in other tissues. Serological analyses show that most, if not all, of the T lymphocytes express the transgenic beta chain on the cell surface and lack beta chains encoded by endogenous beta genes. Molecular genetic analyses of uncloned and cloned T lymphocytes demonstrate that rearrangement of endogenous beta genes is incomplete. Partial D beta 1-J beta 1 rearrangements are found preferentially, while complete VDJ rearrangements are not seen. These findings show that expression of the transgene regulates the rearrangement of endogenous beta genes. Although the alpha beta T cell receptors of the transgenic mice are homogeneous with respect to the beta chain, they are fully functional, at least in a variety of allogeneic responses.
构建了带有功能性T细胞受体β基因的转基因小鼠。导入基因的转录主要局限于T细胞,但在B细胞和其他组织中也能检测到低水平的转录本。血清学分析表明,大多数(如果不是全部的话)T淋巴细胞在细胞表面表达转基因β链,并且缺乏由内源性β基因编码的β链。对未克隆和克隆的T淋巴细胞进行分子遗传学分析表明,内源性β基因的重排是不完全的。优先发现部分Dβ1-Jβ1重排,而未观察到完整的VDJ重排。这些发现表明转基因的表达调节内源性β基因的重排。尽管转基因小鼠的αβT细胞受体在β链方面是同质的,但它们至少在多种同种异体反应中具有完全功能。