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Endocrinology Vol. 139, No. 4 1965-1971
Copyright © 1998 by The Endocrine Society


ARTICLES

Growth Hormone Stimulation of the Mitogen-Activated Protein Kinase Pathway Is Cell Type Specific1

Dexter W. Love, Andrew J. Whatmore, Peter E. Clayton and Corinne M. Silva

Department of Internal Medicine, Division of Endocrinology, University of Virginia (D.W.L., C.M.S.), Charlottesville, Virginia 22908; and the Endocrine Sciences Research Division, Department of Medicine, University of Manchester (P.E.C., A.J.W.), Manchester, United Kingdom M13 9PT

Address all correspondence and requests for reprints to: Dr. Corinne M. Silva, Box 511, Division of Endocrinology, University of Virginia Health Sciences Center, Charlottesville, Virginia 22908. E-mail: cms3e{at}virginia.edu

The GH receptor is a member of the cytokine receptor superfamily. Studies in the 3T3-F442A mouse preadipocyte have shown that GH activates the Janus kinase (JAK2), the signal transducers and activators of transcription (STAT1, -3, and -5), and mitogen-activated protein (MAP) kinase. Our previous studies in the human IM-9 lymphocyte have shown that GH activates JAK2 and only STAT5 (not STAT1 or -3). In the studies presented here, we have investigated activation of the MAP kinase (MAPK) pathway in the IM-9 lymphocyte. Western blotting with antiphosphotyrosine-, anti-MAPK-, and anti-phospho-MAPK-specific antibodies as well in vitro kinase assays using a synthetic peptide substrate demonstrate that although GH (200 ng/ml) activates MAPK in 3T3-F442A cells (at 5 and 10 min of treatment), it does not activate MAPK in IM-9 lymphocytes at time points ranging from 5–60 min. Nevertheless, the phorbol ester phorbol 12-myristate 13-acetate (50 ng/ml) does activate MAPK in the IM-9 cell, and immunoprecipitation with specific antibodies indicates that this activation occurs through c-Raf-1. Although the 52- and 66-kDa forms of the adapter protein Shc are tyrosine phosphorylated in response to GH treatment in 3T3-F442A cells, we demonstrate that the predominant forms in IM-9 cells are the 52- and 46-kDa forms, and neither is tyrosine phosphorylated in response to GH. These studies further elucidate the differential signaling by GH in two cell types.




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