Ceramide Regulates Protein Synthesis by a Novel Mechanism Involving the Cellular PKR Activator RAX

Peter P. Ruvolo, Fengqin Gao, William L. Blalock, Xingming Deng, W. Stratford May

Research output: Contribution to journalArticle

64 Citations (Scopus)

Abstract

The sphingolipid ceramide is an important second signal molecule and potent apoptotic agent. The production of ceramide is associated with virtually every known stress stimulus, and thus, generation of this sphingolipid has been suggested as a universal feature of apoptosis. Recent studies suggest that an important component of cell death following diverse stress stimuli (e.g. interleukin-3 withdrawal, sodium arsenite treatment, and peroxide treatment) is the activation of the double-stranded RNA-activable protein kinase, PKR, resulting in the inhibition of protein synthesis (Ito, T., Jagus, R., and May, W. S. (1994) Proc. Natl. Acad. Sci. U. S. A. 91, 7455-7459). The recently discovered cellular PKR activator, RAX, is phosphorylated in association with PKR activation (Ito, T., Yang, M., and May, W. S. (1999) J. Biol. Chem. 274, 15427-15432). Since RAX is phosphorylated by an as yet undetermined SAPK and ceramide is a potent activator of SAPKs such as JNK, a role for ceramide in the activation of RAX might be possible. Results indicate that overexpression of exogenous RAX potentiates ceramide-induced killing. Furthermore, ceramide can potently inhibit protein synthesis. Since ceramide potently promotes RAX and eukaryotic initiation factor-2α phosphorylation, a possible role for ceramide in this process may involve the activation of PKR by RAX. Since 2-aminopurine, a serine/threonine kinase inhibitor that has previously been shown to inhibit PKR, blocks both the potentiation of ceramide killing by RAX and ceramide-induced inhibition of protein synthesis, ceramide appears to promote PKR activation, at least indirectly. Collectively, these findings suggest a novel role for ceramide in the regulation of protein synthesis and apoptosis.

Original languageEnglish
Pages (from-to)11754-11758
Number of pages5
JournalJournal of Biological Chemistry
Volume276
Issue number15
DOIs
Publication statusPublished - Apr 13 2001

Fingerprint

Ceramides
Proteins
Chemical activation
Sphingolipids
2-Aminopurine
Eukaryotic Initiation Factor-2
eIF-2 Kinase
Apoptosis
Phosphorylation
Double-Stranded RNA
Interleukin-3
Protein-Serine-Threonine Kinases
Peroxides
Cell death
Cell Death
Association reactions

ASJC Scopus subject areas

  • Biochemistry

Cite this

Ceramide Regulates Protein Synthesis by a Novel Mechanism Involving the Cellular PKR Activator RAX. / Ruvolo, Peter P.; Gao, Fengqin; Blalock, William L.; Deng, Xingming; Stratford May, W.

In: Journal of Biological Chemistry, Vol. 276, No. 15, 13.04.2001, p. 11754-11758.

Research output: Contribution to journalArticle

Ruvolo, Peter P. ; Gao, Fengqin ; Blalock, William L. ; Deng, Xingming ; Stratford May, W. / Ceramide Regulates Protein Synthesis by a Novel Mechanism Involving the Cellular PKR Activator RAX. In: Journal of Biological Chemistry. 2001 ; Vol. 276, No. 15. pp. 11754-11758.
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