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14 Chains1 ,2
Sapporo Medical University, School of Medicine, Department of Pathology, Sapporo, Japan
Rat invariant TCR
-chains and NKT cells were
investigated to clarify whether CD1d-mediated recognition by NKT cells
is conserved further in evolution. Rats had multiple-copies of
TRAV14 genes, which can be categorized into two types
according to the diversity accumulated in the CDR2 region. Rats
retained invariant TCR
forms with the homogeneous junctional region
similar to mouse invariant TRAV14-J281. The proportion
of invariant TCR among V
14+ clones was 12.9% in the
thymus and increased in the periphery, 31% in the spleen and 95% in
hepatic sinusoidal cells. The invariant TRAV14-J281 was
expressed by liver sinusoidal and splenic NKT cells with CD8,
CD44high, and TCR Vß8. Type 1 invariant TCR
was
expressed more frequently in hepatic lymphocytes, while type 2
invariant TCR
was expressed predominantly in the spleen. Both types
of cells cytolyzed to and were stimulated to proliferate by
CD1d-expressing cells in a CD1d-restricted manner. These results
suggested that rat NKT cells bearing distinct V
14 chains are
distributed in a tissue-specific pattern. NKT cell populations in rats
were more variable than those in mice, indicating that they play novel
roles in nature. The implication of the molecular interaction between
the structurally diverse invariant TCR
and CD1d/ligand complex in
different organs is discussed.
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