Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
46
pubmed:dateCreated
1997-1-7
pubmed:abstractText
In this report, we demonstrate that insulin receptor substrate-2 (IRS-2) is tyrosyl-phosphorylated following stimulation of 3T3-F442A fibroblasts with growth hormone (GH), leukemia inhibitory factor and interferon-gamma. In response to GH and leukemia inhibitory factor, IRS-2 is immediately phosphorylated, with maximal phosphorylation detected at 15 min; the signal is substantially diminished by 60 min. In response to interferon-gamma, tyrosine phosphorylation of IRS-2 was prolonged, with substantial signal still detected at 60 min. Characterization of the mechanism of signaling utilized by GH indicated that tyrosine residues in GH receptor are not necessary for tyrosyl phosphorylation of IRS-2; however, the regions of GH receptor necessary for IRS-2 tyrosyl phosphorylation are the same as those required for JAK2 association and tyrosyl phosphorylation. The role of IRS-2 as a signaling molecule for GH is further demonstrated by the finding that GH stimulates association of IRS-2 with the 85-kDa regulatory subunit of phosphatidylinositol 3'-kinase and with the protein-tyrosine phosphatase SHP2. These results are consistent with the possibility that IRS-2 is a downstream signaling partner of multiple members of the cytokine family of receptors that activate JAK kinases.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Growth Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Human Growth Hormone, http://linkedlifedata.com/resource/pubmed/chemical/IRS2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Insulin Receptor Substrate Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-6, http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/Irs2 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/LIF protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Leukemia Inhibitory Factor, http://linkedlifedata.com/resource/pubmed/chemical/Lif protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Lymphokines, http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylinositol 3-Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Phosphoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Phosphotransferases (Alcohol Group..., http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
271
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
29415-21
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:8910607-3T3 Cells, pubmed-meshheading:8910607-Animals, pubmed-meshheading:8910607-CHO Cells, pubmed-meshheading:8910607-Cricetinae, pubmed-meshheading:8910607-Growth Inhibitors, pubmed-meshheading:8910607-Human Growth Hormone, pubmed-meshheading:8910607-Humans, pubmed-meshheading:8910607-Insulin Receptor Substrate Proteins, pubmed-meshheading:8910607-Interferon-gamma, pubmed-meshheading:8910607-Interleukin-6, pubmed-meshheading:8910607-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:8910607-Leukemia Inhibitory Factor, pubmed-meshheading:8910607-Lymphokines, pubmed-meshheading:8910607-Mice, pubmed-meshheading:8910607-Phosphatidylinositol 3-Kinases, pubmed-meshheading:8910607-Phosphoproteins, pubmed-meshheading:8910607-Phosphorylation, pubmed-meshheading:8910607-Phosphotransferases (Alcohol Group Acceptor), pubmed-meshheading:8910607-Signal Transduction, pubmed-meshheading:8910607-Tyrosine
pubmed:year
1996
pubmed:articleTitle
Growth hormone, interferon-gamma, and leukemia inhibitory factor utilize insulin receptor substrate-2 in intracellular signaling.
pubmed:affiliation
Department of Physiology, The University of Michigan Medical School, Ann Arbor, Michigan 48109-0622, USA. cartersu@umich.edu
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.