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. 1999 Jun 21;189(12):1907–1921. doi: 10.1084/jem.189.12.1907

Table III.

Strain and Tissue Distribution, and MHC Selection of mAV19-AJ33+ T Cells

Strain Haplotype Lymph nodes Spleen PBLs Thymus Bone marrow Liver IELs Lamina propria
BALB/c H-2d +++ + +++ + +
I-A+/I-E+
DBA/2 H-2d +++
I-A+/I-E+
CBA H-2k +++ +
I-A+/I-E+
129 H-2b + +++
I-A+/I-E
C57BL/6 H-2b +++ +++ +
I-A+/I-E
NUDE B6 H-2b
I-A+/I-E
B6 I-Ab−/− β2m−/− Kb−/−/Db−/− TAP−/− CD1−/− CD8−/−
mAV19-AJ33 ++ ++ ++ +++ ++ ++
 (fold increase (2) (4) (8) (2) (4)
 compared with B6)
mAV14-AJ18 ++ ++ ++ ++ ++

DN α/β+/+ T cells were purified from the indicated organs in different mouse strains. Expression of the invariant mAV19-AJ33 TCR α chain was estimated by quantitative kinetic PCR and confirmed by polyclonal sequencing (see Materials and Methods, and Figs. 1 and 2). Tissue distribution results are compared with the expression in sorted CD4+ α/β+ T cells: +++, high expression (>3-cycle shift to the left); +, no increase; −, absence as judged by polyclonal sequencing of mAV19-AJ33 amplicons. Selection results (bottom) in the lymph nodes of the different MHC-deficient mice are compared with the expression in DN cells from B6 lymph nodes using quantitative PCR. All of the results were also confirmed by polyclonal sequencing after mAV19-Cα, or -AJ33 amplification as appropriate.