Activation of Acute Phase Response Factor (APRF)/Stat3 Transcription Factor by Growth Hormone

• Published in: The Journal of biological chemistry Vol. 270; no. 8; pp. 3974 - 3979
• Main Authors: Campbell, G S, Meyer, D J, Raz, R, Levy, D E, Schwartz, J, Carter-Su, C
• Format: Journal Article
• Language: English
• Published: United States American Society for Biochemistry and Molecular Biology 24.02.1995
• Subjects: 3T3 Cells; Animals; Base Sequence; Cell Nucleus - drug effects; Cell Nucleus - metabolism; DNA-Binding Proteins - metabolism; Growth Hormone - pharmacology; Mice; Molecular Sequence Data; Oligodeoxyribonucleotides; Phosphorylation; STAT3 Transcription Factor; Trans-Activators - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.270.8.3974

The mechanisms by which the binding of growth hormone (GH) to its cell surface receptor elicits changes in gene transcription are largely unknown. The transcription factor Stat1/p91 has been shown to be activated by GH. Here we show that acute phase response factor or Stat3 (or an antigenically related protein), is also activated by GH. Stat3 has been implicated in the interleukin-6-dependent induction of acute phase response genes. GH promotes in 3T3-F442A fibroblasts the tyrosyl phosphorylation of a protein immunoprecipitated by antibodies to Stat3. This protein co-migrates with a tyrosyl phosphorylated protein from cells treated with leukemia inhibitory factor, a cytokine known to activate Stat3. Tyrosyl phosphorylated Stat3 is also observed in response to interferon- . Stat3 is present in GH-inducible DNA-binding complexes that bind the sis -inducible element in the c- fos promoter and the acute phase response element in the α 2 -macroglobulin promoter. The ability of GH to activate both Stat1 and Stat3 ( i.e. increase their tyrosyl phosphorylation and ability to bind to DNA) suggests that gene regulation by GH involves multiple Stat proteins. Shared transcription factors among hormones and cytokines that activate JAK kinases provide an explanation for shared responses, while the ability of the different ligands to differentially recruit various Stat family members suggests mechanisms by which specificity in gene regulation could be achieved.