Expression of a dominant interfering mutant of MAP kinase kinase (MAPKK) inhibits interleukin-3 (IL-3) activation of MAP kinase in the murine bone marrow-derived cell line BAF3. This results in an increase in the level of IL-3 required to stimulate cell proliferation and suppress apoptosis. When apoptosis is constitutively inhibited by coexpression of bcl-2, the dominant interfering MAPKK inhibits IL-3 driven cell cycle progression. Thus, MAPKK function is necessary for optimal IL-3 inhibition of apoptosis and optimal IL-3 stimulation of entry into S phase. Expression of a constitutively activated mutant of MAPKK does not replace IL-3, but renders cells able to proliferate in a density-dependent manner. Cell contact is required to allow cell proliferation; such contact can be supplied by cells without activated MAPKK.
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May 1, 1996
The role of MAP kinase kinase in interleukin-3 stimulation of proliferation
GR Perkins,
GR Perkins
CRC Centre for Cell and Molecular Biology, Chester Beatty Laboratories, London, UK.
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CJ Marshall,
CJ Marshall
CRC Centre for Cell and Molecular Biology, Chester Beatty Laboratories, London, UK.
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MK Collins
MK Collins
CRC Centre for Cell and Molecular Biology, Chester Beatty Laboratories, London, UK.
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Blood (1996) 87 (9): 3669–3675.
Citation
GR Perkins, CJ Marshall, MK Collins; The role of MAP kinase kinase in interleukin-3 stimulation of proliferation. Blood 1996; 87 (9): 3669–3675. doi: https://doi.org/10.1182/blood.V87.9.3669.bloodjournal8793669
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May 1 1996
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