Detection of CD45iota mRNA in murine Th1 but not Th2 clones

Citation
K. Tsujikawa et al., Detection of CD45iota mRNA in murine Th1 but not Th2 clones, IMMUNOBIOL, 201(5), 2000, pp. 506-514
Citations number
25
Categorie Soggetti
Immunology
Journal title
IMMUNOBIOLOGY
ISSN journal
01712985 → ACNP
Volume
201
Issue
5
Year of publication
2000
Pages
506 - 514
Database
ISI
SICI code
0171-2985(200004)201:5<506:DOCMIM>2.0.ZU;2-C
Abstract
CD45, a prototype of the receptor-like protein tyrosine phosphatase (PTPase ) family, is one of the essential molecules in signal transduction through T cell receptors. Because at least 8 types of CD45 isoforms can potentially be produced by alternative mRNA splicing of exons 4, 5, and 6, the analyse s at the transcription and protein levels of CD45 during the development an d differentiation of T cells have been performed using RT-PCR and isoform-s pecific monoclonal antibodies, respectively. We report here that the ninth and smallest isoform of CD45, designated as CD45iota (CD45 iota), which is alternatively spiced from exons 4, 5, and 6 as well as exon 7, is present i n the fetal thymus and splenic T cells of mice, and in murine Th1 clones, b ut not in Th2 clones. The expression of full-length CD45 iota mRNA as the f unctional CD45 PTPase was confirmed by RT-PCR analysis. Furthermore, the ex pression vector of CD45 iota was constructed, and its expression was detect ed in combination with anti-pan CD45 mAb and our newly established anti-LAR /CD45 PTPase domain mAb. These results suggested chat CD45 iota might be an important isoform of CD45 for differentiation signaling of Th cells, and m ight be used as a marker to distinguish between Th1 and Th2 cells.