The Regulation and Role of c-FLIP in Human Th Cell Differentiation
Author(s) -
Minna K. Kyläniemi,
Riina Kaukonen,
Johanna Myllyviita,
Omid Rasool,
Riitta Lahesmaa
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0102022
Subject(s) - gene knockdown , microbiology and biotechnology , cellular differentiation , gene isoform , transcription factor , biology , flip , gata3 , apoptosis , biochemistry , gene
The early differentiation of T helper (Th) cells is a tightly controlled and finely balanced process, which involves several factors including cytokines, transcription factors and co-stimulatory molecules. Recent studies have shown that in addition to the regulation of apoptosis, caspase activity is also needed for Th cell proliferation and activation and it might play a role in Th cell differentiation. The isoforms of the cellular FLICE inhibitory protein (c-FLIP) are regulators of CASPASE-8 activity and the short isoform, c-FLIP S , has been shown to be up-regulated by IL-4, the Th2 driving cytokine. In this work, we have studied the expression and functional role of three c-FLIP isoforms during the early Th cell differentiation. Only two of the isoforms, c-FLIP S and c-FLIP L , were detected at the protein level although c-FLIP R was expressed at the mRNA level. The knockdown of c-FLIP L led to enhanced Th1 differentiation and elevated IL-4 production by Th2 cells, whereas the knockdown of c-FLIP S diminished GATA3 expression and IL-4 production by Th2 cells. In summary, our results provide new insight into the role of c-FLIP proteins in the early differentiation of human Th cells.
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