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PMID: 9647201 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The expression in vivo of a second isoform of pT alpha: implications for the mechanism of pT alpha action.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 161 ·No. 1 ·1998-07-01 ·Pages 11-6

Barber DF, Passoni L, Wen L, Geng L, Hayday AC

Abstract

A second isoform of pT alpha, "pT alpha(b)," is derived from the pT alpha locus by tissue-specific, alternative splicing. pT alpha(b) is coexpressed in the thymus with the previously characterized form of pT alpha (which we term pT alpha(a)) and is also expressed in peripheral cells without pT alpha(a). While pT alpha(a) acts to retain most TCR beta-chains intracellularly, pT alpha(b) permits higher levels of cell surface TCR beta expression and facilitates signaling from a CD3-TCR beta complex.

MeSH Terms
Alternative Splicing Animals Cell Separation Clone Cells Isomerism Lymphocyte Activation/genetics Membrane Glycoproteins/biosynthesis,genetics,physiology Mice Mice, Knockout RNA, Messenger/biosynthesis Receptors, Antigen, T-Cell, alpha-beta/biosynthesis,genetics,physiology Signal Transduction/genetics,immunology T-Lymphocyte Subsets/immunology,metabolism
Chemicals
Membrane Glycoproteins RNA, Messenger Receptors, Antigen, T-Cell, alpha-beta pre-T cell receptor alpha
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Barber D F
Department of Molecular, Cell & Developmental Biology, Yale University, New Haven, CT 06520, USA.
Passoni L
Wen L
Geng L
Hayday A C
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1998-07-01
Pages
11-6
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIGMS NIH HHS · GM37759 · United States
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