Premium
Variability of CD3 membrane expression and T cell activation capacity
Author(s) -
El Hentati FatimaZahra,
Gruy Frederic,
Iobagiu Cristina,
Lambert Claude
Publication year - 2010
Publication title -
cytometry part b: clinical cytometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.646
H-Index - 61
eISSN - 1552-4957
pISSN - 1552-4949
DOI - 10.1002/cyto.b.20496
Subject(s) - cd3 , flow cytometry , cd8 , t cell , microbiology and biotechnology , biology , chemistry , immunology , antigen , immune system
Background: αβT cells have a wide distribution of CD3 membrane density. The aim of this article was to evaluate the significance of the CD3 differential expression on T cell subsets. Analysis was performed on healthy donors and renal transplant patients by flow cytometry. The results obtained are: (1) CD3 expression was widely distributed (CV = 38.3 ± 3.1 to 43 ± 2.3%). (2) The CD4, CD8, CD45 and forward scatter were similarly distributed. (3) The diversity of CD3 expression was directly related to the clonotypes: γ9, non γ9 from γδT cells and Vβ clonotype from αβT cells (e.g., Vβ3FITC 7,980 ± 1,628 Vβ8PE: Vβ20‐FITC 11,768 ± 1,510). (4) Using a computer simulation, we could confirm differential kinetics of T cell activation according to the initial parameters. Finally, in vitro activation was significantly higher on Vβ8 and Vβ9 (high CD3) compared with Vβ2 and Vβ3 (low CD3, P = 0.040–0.0003). In conclusion, T cells have highly heterogeneous CD3 expression, possibly predetermined and with clear functional significance. © 2009 Clinical Cytometry Society
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom