Exp Mol Med.
1998 Sep;30(3):159-164.
Endoplasmic reticulum retention and degradation of T cell antigen receptor beta
chain
- Affiliations
-
- 1Department of Biochemistry, Kosin Medical College, Pusan, Korea.
Abstract
- The T cell antigen receptor-CD3 (TCR/CD3) complex is assembled in the
endoplasmic reticulum (ER) of T cells after synthesis of individual chains, and
is transported to the cell surface for immune recognition and regulation.
Partially assembled or unassembled TCR chains are retained and rapidly degraded
in the ER. These processes are strictly regulated in the ER at
post-translational level for the maintenance of cellular homeostasis. In order
to identify the region responsible for the ER retention and rapid degradation of
the TCR beta chain, number of mutants were engineered and their fates, after
synthesis in the ER of the HeLa cells, were investigated. Extensive mutagenic
analysis of TCR beta chain, including changing the charged amino acid residues
and two tyrosine residues of the transmembrane region into hydrophobic amino
acid residues, did not alter the ER retention and rapid degradation. Soluble TCR
beta chain and cytoplasmic tail truncation mutant were also rapidly degraded in
the ER. However, N-glycosylation rate of soluble TCR beta chain in the ER was
significantly increased possibly due to the increased exposure of the
N-glycosylation site. These results suggest that the ER retention of TCR beta
chain is mediated through its extracellular and transmembrane-cytoplasmic
regions and that the rapid ER degradation can be caused by an exposure of
unassembled subregion of TCR beta chain, either extracellular domain or
hydrophobic transmembrane region to the hydrophilic environment (lumen of the
ER) rather than by presence of a specific degradation signal.