Impaired NK1.1 T cell development in mice transgenic for a T cell receptorbeta chain lacking the large, solvent-exposed C beta FG loop

Citation
S. Degermann et al., Impaired NK1.1 T cell development in mice transgenic for a T cell receptorbeta chain lacking the large, solvent-exposed C beta FG loop, J EXP MED, 190(9), 1999, pp. 1357-1362
Citations number
31
Categorie Soggetti
Medical Research General Topics
Journal title
JOURNAL OF EXPERIMENTAL MEDICINE
ISSN journal
00221007 → ACNP
Volume
190
Issue
9
Year of publication
1999
Pages
1357 - 1362
Database
ISI
SICI code
0022-1007(19991101)190:9<1357:INTCDI>2.0.ZU;2-J
Abstract
A striking feature of the T cell receptor (TCR) beta chain structure is the : large FG loop that protrudes freely into the solvent on the external face of the C beta domain. We have already shown that a transgene-encoded V bet a 8.2(+) TCR beta chain lacking the complete C beta FG loop supports normal development and function of conventional alpha/beta T cells. Thus, the FG loop is not absolutely necessary for TCR signaling. However, further analys is has revealed that a small population of alpha/beta T cells coexpressing NK1.1 are severely depleted in these transgenic mice. The few remaining NK1 .1 T cells have a normal phenotype but express very low levels of TCR. We f ind that the TCR V beta 8.2(+) chain lacking the C beta FG loop cannot pair efficiently with the invariant Va14-Jol281 TCR alpha chain commonly expres sed by this T cell family. Consequently, fewer NK1.1 T cells develop in the se mice. Our results suggest that expression of the V alpha 14(+) TCR alpha chain is particularly sensitive to TCR-beta conformation. Development of N K1.1 T cells appears to need a TCR-beta conformation dependent on the prese nce of the C beta loop that is not necessarily required for assembly and fu nction of TCRs on most alpha/beta T cells.