Hz. Hu et al., EXPRESSION OF T-CELL RECEPTOR-ALPHA AND BETA-VARIABLE GENES IN NORMALAND MALIGNANT HUMAN T-CELLS, British Journal of Haematology, 84(1), 1993, pp. 39-48
A PCR method was developed to analyse each of 29 families of the T cel
l receptor Valpha gene and 20 families of the Vbeta gene at the mRNA l
evel in heterogenous cell populations. All Valpha and Vbeta families w
ere detectable in blood mononuclear cells from four of six healthy don
ors. In two donors only Valpha22 was missing, and all other Valpha and
Vbeta families were detected. Vbeta family expression was observed in
T-leukaemic cell lines Jurkat, HSB, Molt-3 and Molt-4. In contrast, V
alpha family expression was not detectable in any cell line except Jur
kat cells. In T-cell malignancies (non-Hodgkin's lymphoma and mycosis
fungoides), one or two Valpha and Vbeta families were detectable. Four
of 10 cases investigated showed two Va transcripts and one Vbeta tran
script. This fits with concepts in literature that allelic exclusion f
or the genes encoding alpha chains is not strictly required in the DNA
rearrangement, or that this exclusion is a post-translational event.
Using a limited series of antibodies to Vbeta gene family products, bl
ood mononuclear cells from healthy donors were analysed by flow cytome
try in a follow-up study. Two of four donors were rather stable in pro
portions of T cells expressing distinct Vbeta families, and two other
donors showed variation in one or more families. When analysed on froz
en tissue sections of normal lymph node and tonsil, there was no prefe
rential location of lymphocytes expressing a distinct Vbeta gene famil
y in different compartments (interfollicular area, follicle, or tonsil
lar epithelium).