Comparative analysis of CD8 expressed on mature CD4+ CD8+ T cell clones cultured with IL-4 and that on CD8+ T cell clones: implication for functional significance of CD8 beta

• Published in: International immunology Vol. 3; no. 7; p. 737
• Main Authors: Hori, T, Paliard, X, de Waal Malefijt, R, Ranes, M, Spits, H
• Format: Journal Article
• Language: English
• Published: England 01.07.1991
• Subjects: CD4 Antigens; CD8 Antigens - chemistry; CD8 Antigens - genetics; Cell Differentiation; Clone Cells - immunology; Gene Expression Regulation; Humans; Interleukin-4 - pharmacology; Protein Conformation; RNA, Messenger - genetics; T-Lymphocyte Subsets - cytology; T-Lymphocyte Subsets - immunology
• ISSN: 0953-8178
• DOI: 10.1093/intimm/3.7.737

Interleukin (IL-4) can induce CD8 expression on mature CD4+ T cells. To study this phenomenon in more detail, we characterized CD8 expressed on IL-4-induced CD4+ CD8+ (double positive) T cell clones in comparison with that on CD8+ T cell clones. Using 2ST8-5H7 mAb that detects CD8 beta expression, we found that double positive T cell clones isolated with IL-4 express CD8 alpha but not beta, in contrast to CD8+ CTL cell clones, which express both chains of CD8. Northern blot analysis revealed that these double positive clones expressed CD8 alpha but not beta mRNA, indicating that CD8 alpha and beta are independently regulated at the pre-translational level. Immunoprecipitation experiments showed that CD8 expressed on a representative IL-4-induced double positive T cell clone consists mainly of homodimers of a single 34 kd protein of CD8 alpha. The amount of multimers detected from this clone was much less than that from a CD8+ CTL clone. These results suggest that persistent expression of CD8 beta is specific for the CD8+ lineage and may be involved in polymerization and stabilization of CD8 which enhances the efficiency of class I-restricted antigen recognition.