Involvement of protein phosphatase 2A in the interleukin-3-stimulated Jak2-Stat5 signaling pathway.
In this study, we report that the tyrosine kinase, Janus kinase 2 (Jak2), associates with the serine/threonine protein phosphatase 2A (PP2A) in 32Dcl3 myeloid progenitor cells. The association between Jak2 and PP2A transiently increases following interleukin-3 (IL-3) stimulation and activation of Jak2. The catalytic subunit of PP2A is tyrosine phosphorylated ... by Jak2 in vitro and in vivo, resulting in inhibition of phosphatase activity. PP2A also associates with Stat5 in 32Dcl3 cells in an IL-3-dependent manner. Pretreatment of 32Dcl3 cells with okadaic acid (OA), an inhibitor of PP2A, resulted in increased tyrosine phosphorylation and nuclear translocation of Stat5. Our results suggest that PP2A plays a negative regulatory role in regulating the IL-3 signaling pathway via formation of complexes with Jak2 and Stat5.
Mesh Terms:
Animals, Biological Transport, Active, Cell Line, Cell Nucleus, DNA-Binding Proteins, Enzyme Inhibitors, Hematopoietic Stem Cells, Interleukin-3, Janus Kinase 2, Macromolecular Substances, Mice, Milk Proteins, Models, Biological, Okadaic Acid, Phosphoprotein Phosphatases, Phosphorylation, Protein Phosphatase 2, Protein-Tyrosine Kinases, Proto-Oncogene Proteins, Recombinant Proteins, STAT5 Transcription Factor, Signal Transduction, Trans-Activators, Tyrosine
Animals, Biological Transport, Active, Cell Line, Cell Nucleus, DNA-Binding Proteins, Enzyme Inhibitors, Hematopoietic Stem Cells, Interleukin-3, Janus Kinase 2, Macromolecular Substances, Mice, Milk Proteins, Models, Biological, Okadaic Acid, Phosphoprotein Phosphatases, Phosphorylation, Protein Phosphatase 2, Protein-Tyrosine Kinases, Proto-Oncogene Proteins, Recombinant Proteins, STAT5 Transcription Factor, Signal Transduction, Trans-Activators, Tyrosine
J. Interferon Cytokine Res.
Date: Jun. 01, 2001
PubMed ID: 11440634
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