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J. Biol. Chem., Vol. 277, Issue 26, 23544-23553, June 28, 2002
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From the The thrombopoietin (TPO) receptor c-Mpl,
like other members of the cytokine receptor superfamily, requires the
association and activation of Janus kinases (JAKs) for normal signal
transduction. The membrane-proximal portion of the signaling domain,
containing conserved box1 and box2 motifs, is sufficient to support the
proliferation of cytokine-dependent cell lines and basal
megakaryocytopoiesis in vivo. We hypothesized that
activation of the JAK2 kinase alone might be sufficient for
proliferative signaling. To test this premise, we constructed chimeric
receptors in which the extracellular and transmembrane portions of Mpl
were fused to the pseudokinase and kinase domains of murine JAK2
kinase. When expressed in the interleukin-3-dependent cell
line Ba/F3, the chimeric receptors were appropriately expressed on the
cell surface and were able to initiate tyrosine kinase activity upon
exposure to TPO. However, chimeric receptors lacking an intact box2
domain of Mpl were unable to support proliferation at any concentration
of TPO. Only chimeric receptors containing both JAK2 kinase activity
and the box2 region initiated proliferative signaling. Within the box2
motif, we determined that the sequence
Glu56-Ile57-Leu58 of the Mpl
cytoplasmic domain is critical for proliferation of the chimeric
receptors. Furthermore, TPO-dependent induction of c-myc transcription is also dependent on this motif. These
results indicate that JAK2 activation alone is not sufficient for
TPO-induced proliferation and that one or more essential signaling
pathways must arise from the cytoplasmic domain of Mpl that includes
box2. Although the nature of the signal transduction pathway is not yet
known, this second proliferative event is likely to regulate c-myc expression.
Studies with Chimeric Mpl/JAK2 Receptors Indicate That Both JAK2
and the Membrane-proximal Domain of Mpl Are Required for Cellular
Proliferation*
§¶,
,
,
§,
Puget Sound Blood Center, Seattle,
Washington 98104 and the § University of Washington,
School of Medicine, Seattle, Washington 98195
*
This work was supported by United States Public Health
Service Grants K08 HL03498 and R01 HL65498 (to J. G. D.) and Grant R01 CA31615 (to K. K.).The costs of publication of this
article were defrayed in part by the
payment of page charges. The article must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
Present address: Div. of Hematology, Keio University School of
Medicine, Tokyo 160-8582, Japan.
**
Present address: Dept. of Medicine, University of California
at San Diego, La Jolla, CA 92093.
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