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CD3[sup [minus]] T cells with cis- or trans-acting mutations affecting expression of T cell receptor [beta]-chain mRNA

Journal Article · · Journal of Immunology; (United States)
OSTI ID:7064004
;  [1]; ;  [2]
  1. Harvard Medical School, Boston, MA (United States)
  2. Dana-Farber Cancer Inst., Boston, MA (United States)
Mutants of an untransformed T cell clone that no longer respond to TCR/CD3 stimulation have been derived using a selection procedure based on the loss of functional response to Ag. This functional selection gives rise to clones of several different phenotypes. The authors have previously described mutants with a TCR/CD3[sup +] cell surface phenotype whose TCR are uncoupled from cellular responses. They describe six additional mutants that do not express TCR/CD3 at the cell surface. One of the CD3[sup [minus]] clones contains a deletion in the successfully rearranged TCR-[alpha] gene, whereas another carries a deletion in the successfully rearranged TCR-[beta] gene. TCR/CD3 expression in these deletion mutants can be restored by transfection of TCR-[alpha] or TCR-[beta] DNA. Four other clones do not express TCR-[beta] mRNA, yet contain no obvious deletions or rearrangements in the TCR-[beta] genes. One of these clones does not transcribe TCR-[beta] chain mRNA. The mutation in this clone does not reside in a trans-acting regulatory element affecting TCR-[beta] gene expression, because the TCR-[beta] mRNA[sup [minus]] phenotype is complemented by fusion with a TCR-[alpha][sup [minus]][beta][sup [minus]] cell line. TCR-[beta] chain regulatory mutants will be valuable in contributing to our understanding of how TCR expression is regulated. 33 refs., 6 figs., 1 tab.
OSTI ID:
7064004
Journal Information:
Journal of Immunology; (United States), Journal Name: Journal of Immunology; (United States) Vol. 149:12; ISSN JOIMA3; ISSN 0022-1767
Country of Publication:
United States
Language:
English