Cutting Edge: Protein Kinase Cβ Expression Is Critical for Export of IL-2 from T Cells
Author(s) -
Aideen Long,
Dermot Kelleher,
Sara Lynch,
Yuri Volkov
Publication year - 2001
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.167.2.636
Subject(s) - protein kinase c , secretion , microbiology and biotechnology , biology , clone (java method) , gene isoform , cell culture , kinase , gene , biochemistry , genetics
Protein kinase C (PKC) plays an integral part in T cell activation and IL-2 secretion. We investigated the role of a particular PKC isoform, PKCbeta, in IL-2 production and secretion. The T cell lymphoma line HuT 78 secretes IL-2 in response to the phorbol ester PMA. A PKCbeta-deficient clone of HuT 78, K-4, did not secrete IL-2 in response to PMA stimulation. As assessed by RT-PCR, K-4 expressed mRNA for IL-2 following PMA activation, and intracellular IL-2 protein was detected by immunofluorescence. An enhanced green fluorescent protein-linked PKCbeta construct was microinjected into K-4 cells, which were then stimulated with PMA; those cells that expressed PKCbeta could secrete IL-2, as determined by an in situ immunofluorescent assay. This study demonstrates that PKCbeta is not necessary for transcription of the IL-2 gene or translation of mRNA to protein, but that expression of this PKC isoform is critical to the export of IL-2 molecules from T cells.
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