Growth signaling and JAK2 association mediated by membrane-proximal cytoplasmic regions of prolactin receptors
Prolactin (PRL) has recently been demonstrated to induce tyrosine phosphorylation and activation of the cytoplasmic tyrosine kinase JAK2 in PRL-dependent Nb2 lymphoma cells. The present study represents an initial effort to identify cytoplasmic regions of the PRL receptor (PRLR) that are critical to...
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Veröffentlicht in: | The Journal of biological chemistry 1994-07, Vol.269 (28), p.18267-18270 |
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Sprache: | eng |
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Zusammenfassung: | Prolactin (PRL) has recently been demonstrated to induce tyrosine phosphorylation and activation of the cytoplasmic tyrosine
kinase JAK2 in PRL-dependent Nb2 lymphoma cells. The present study represents an initial effort to identify cytoplasmic regions
of the PRL receptor (PRLR) that are critical to growth signal generation and JAK2 activation. Variably truncated rat PRLRs
were stably expressed in the murine 32D cell line. PRL-induced proliferation was mediated by the full-length receptor and
the mutant G328, which contains the membrane-proximal Homology Boxes 1 and 2 characteristic of hematopoietin receptors. In
contrast, mutant receptors lacking either Box 2 or both Boxes 1 and 2 were not capable of transmitting a growth signal. The
mitogenic capacity of the PRLR variants correlated with JAK2 association and activation, as well as with induction of mRNA
levels for the growth-related gene ornithine decarboxylase. We conclude that mitogenic competence of rat PRLRs resides within
the first 94 amino acids of the cytoplasmic domain. The data suggest that Homology Box 1/Box 2 region is critical to JAK2
phosphorylation and association with the PRLR. These findings will serve as a basis for more detailed molecular characterization
of PRLR domains essential for JAK2 interaction and growth signal generation. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1016/s0021-9258(17)32296-2 |