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Functional expression cloning reveals a central role for the receptor for activated protein kinase C 1 (RACK1) in T cell apoptosis

Mourtada-Maarabouni, Mirna; Kirkham, Lucy; Farzaneh, Farzin; Williams, Gwyn T

Authors

Lucy Kirkham

Farzin Farzaneh

Gwyn T Williams



Contributors

M. Mourtada-Maarabouni
Other

L. Kirkham
Other

F. Farzaneh
Other

G.T. Williams
Other

Abstract

Mammalian cDNA expression cloning was used to identify novel genes that regulate apoptosis. Using a functional screen, we identified a partial cDNA for the receptor for activated protein kinase C 1 (RACK1) through selection for resistance to phytohemagglutinin and γ-irradiation. Expression of this partial cDNA in T cell lines using a mammalian expression vector produced an increase in RACK1 expression and resulted in resistance to dexamethasone- and ultraviolet-induced apoptosis. Down-regulation of RACK1 using RNA interference abolished the resistance of the transfected cells to apoptosis. Overexpression of full-length RACK1 also resulted in the suppression of apoptosis mediated by several apoptotic stimuli, and this effect was quantitatively consistent with the effects of the original cDNA isolated on endogenous RACK1 levels. Together, these findings suggest that RACK1 plays an important role in the intracellular signaling pathways that lead to apoptosis in T cells.

Citation

Mourtada-Maarabouni, M., Kirkham, L., Farzaneh, F., & Williams, G. T. (2005). Functional expression cloning reveals a central role for the receptor for activated protein kinase C 1 (RACK1) in T cell apoptosis. Journal of Leukocyte Biology, 78(2), 503–514. https://doi.org/10.1189/jlb.0205070

Journal Article Type Article
Acceptance Date Apr 1, 2005
Online Publication Date May 3, 2005
Publication Date 2005-08
Deposit Date May 16, 2024
Journal Journal of Leukocyte Biology
Print ISSN 0741-5400
Publisher Society for Leukocyte Biology
Peer Reviewed Peer Reviewed
Volume 78
Issue 2
Pages 503–514
ISBN 07415400
DOI https://doi.org/10.1189/jlb.0205070
Public URL https://keele-repository.worktribe.com/output/543784
Publisher URL https://academic.oup.com/jleukbio/article/78/2/503/6922433