Shiga toxins activate translational regulation pathways in intestinal epithelial cells
| Autor: | W.E. Colpoys, Tessa M. Carducci, Brent H. Cochran, Cheleste M. Thorpe |
|---|---|
| Rok vydání: | 2005 |
| Předmět: |
Hyperphosphorylation
Cell Cycle Proteins P70-S6 Kinase 1 Protein Serine-Threonine Kinases Biology Shiga Toxins p38 Mitogen-Activated Protein Kinases Cell Line Tumor Translational regulation Protein biosynthesis Humans RNA Messenger Intestinal Mucosa Phosphorylation Adaptor Proteins Signal Transducing Sirolimus Aniline Compounds Mitogen-Activated Protein Kinase 3 Ribosomal Protein S6 Kinases EIF4E Intracellular Signaling Peptides and Proteins Translation (biology) Cell Biology Phosphoproteins Molecular biology Cell biology Eukaryotic Initiation Factor-4E Purines Protein Biosynthesis Signal transduction Carrier Proteins |
| Zdroj: | Cellular Signalling. 17:891-899 |
| ISSN: | 0898-6568 |
| Popis: | Shiga toxins (Stxs) cause irreversible damage to eukaryotic ribosomes, yet cellular intoxication of intestinal epithelial cells (IECs) results in increased synthesis of selected proteins, notably cytokines. How mRNA translation is maintained in this circumstance is unclear. This study was designed to assess whether Stx-induced alterations in host signal transduction machinery permit translation despite protein synthesis inhibition. A key step of translation is recruitment of initiation machinery to the 5′ mRNA cap. This event occurs in part via interaction of the 5′ cap with the cap binding protein, eIF4E, whose activity is positively regulated by phosphorylation and negatively regulated by binding to the translational repressor 4E-BP1. Following Stx treatment of IECs, eIF4E phosphorylation was detected by Western blotting using phospho-specific antibodies. Treatment with the p38 inhibitor, SB202190, or either of the ERK1/2 inhibitors, PD98059 and U0126, partially blocked Stx1-induced eIF4E phosphorylation. The Mnk1 inhibitor, CGP57380, blocked both basal and Stx-induced eIF4E phosphorylation. Interestingly, pretreatment with CGP57380 did not alter basal protein synthesis, but diminished the ability of cells to maintain translation following Stx1 challenge. Stx1 also induced hyperphosphorylation of 4E-BP1 and phosphorylation of S6Kinase; both effects were blocked by rapamycin. These data are novel observations showing that Stxs regulate multiple signal transduction pathways controlling translation in host cells, and support a role for eIF4E phosphorylation in maintaining host cell translation despite ribosomal intoxication. |
| Databáze: | OpenAIRE |
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