نتایج جستجو برای: and irs

تعداد نتایج: 16828019  

Journal: :Molecular endocrinology 2003
HongZhi Sun Xiao Tu Marco Prisco An Wu Ivan Casiburi Renato Baserga

The insulin receptor substrate 1 (IRS-1) can translocate to the nuclei and nucleoli of several types of cells. Nuclear translocation can be induced by an activated insulin-like growth factor 1 receptor (IGF-IR), and by certain oncogenes, such as the Simian virus 40 T antigen and v-src. We have asked whether IRS-2 could also translocate to the nuclei. In addition, we have studied the effects of ...

Journal: :The Journal of biological chemistry 2000
P Lebrun V Baron C R Hauck D D Schlaepfer E Van Obberghen

Integrins are transmembrane receptors involved in interactions between cells and extracellular matrix proteins. Here we show that cell adhesion regulates insulin receptor substrate-1 (IRS-1) mRNA synthesis. When fibroblasts are held in suspension, lower levels of IRS-1 mRNA, but not of IRS-2 mRNA, are detected, and this effect is due to the negative regulation of IRS-1 transcription rather than...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 1998
M H Lima J E Zambelli C R Carvalho M J Saad

Insulin stimulates the tyrosine kinase activity of its receptor resulting in the phosphorylation of its cytosolic substrate, insulin receptor substrate-1 (IRS-1) which, in turn, associates with proteins containing SH2 domains. It has been shown that IRS-1 associates with the tyrosine phosphatase SHPTP2 in cell cultures. While the effect of the IRS-1/SHPTP2 association on insulin signal transduc...

Journal: :The Biochemical journal 2002
Duraisamy Senthil Goutam Ghosh Choudhury Basant K Bhandari Balakuntalam S Kasinath

Vascular endothelial growth factor (VEGF) isoforms exert their biological effects through receptors that possess intrinsic tyrosine kinase activity. Whether VEGF binding to its receptors recruits insulin receptor substrate (IRS) family of docking proteins to the receptor is not known. Following incubation of mouse kidney proximal tubular epithelial cells with VEGF, we observed an increase in ty...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
H Eldar-Finkelman E G Krebs

The phosphorylation of insulin receptor substrate 1 (IRS-1) on tyrosine residues by the insulin receptor (IR) tyrosine kinase is involved in most of the biological responses of insulin. IRS-1 mediates insulin signaling by recruiting SH2 proteins through its multiple tyrosine phosphorylation sites. The phosphorylation of IRS-1 on serine/threonine residues also occurs in cells; however, the parti...

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2015
Hsin-Yun Sun Barbara D Alexander Shirish Huprikar Graeme N Forrest Didier Bruno G Marshall Lyon Dannah Wray Leonard B Johnson Costi D Sifri Raymund R Razonable Michele I Morris Valentina Stosor Marilyn M Wagener Nina Singh

BACKGROUND Risk factors including how changes in immunosuppression influence the occurrence of immune reconstitution syndrome (IRS) in solid organ transplant (SOT) recipients with cryptococcosis have not been fully defined. METHODS SOT recipients with cryptococcosis were identified and followed for 12 months. IRS was defined based on previously proposed criteria. RESULTS Of 89 SOT recipient...

2013
Jun Shirakawa Yu Togashi Eri Sakamoto Mitsuyo Kaji Kazuki Tajima Kazuki Orime Hideaki Inoue Naoto Kubota Takashi Kadowaki Yasuo Terauchi

The derangement of endoplasmic reticulum (ER) homeostasis triggers β-cell apoptosis, leading to diabetes. Glucokinase upregulates insulin receptor substrate 2 (IRS-2) expression in β-cells, but the role of glucokinase and IRS-2 in ER stress has been unclear. In this study, we investigated the impact of glucokinase activation by glucokinase activator (GKA) on ER stress in β-cells. GKA administra...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2001
O N Ozes H Akca L D Mayo J A Gustin T Maehama J E Dixon D B Donner

Tyrosine phosphorylation of insulin receptor substrate-1 (IRS-1) by the insulin receptor permits this docking protein to interact with signaling proteins that promote insulin action. Serine phosphorylation uncouples IRS-1 from the insulin receptor, thereby inhibiting its tyrosine phosphorylation and insulin signaling. For this reason, there is great interest in identifying serine/threonine kina...

Journal: :Diabetes 2001
Y Tsuji Y Kaburagi Y Terauchi S Satoh N Kubota H Tamemoto F B Kraemer H Sekihara S Aizawa Y Akanuma K Tobe S Kimura T Kadowaki

To clarify the roles of insulin receptor substrate (IRS) family proteins in phosphatidylinositol (PI) 3-kinase activation and insulin actions in adipocytes, we investigated the intracellular localization of IRS family proteins and PI 3-kinase activation in response to insulin by fractionation of mouse adipocytes from wild-type and IRS-1 null mice. In adipocytes from wild-type mice, tyrosine-pho...

2012
Sabine S. Neukamm Rachel Toth Nick Morrice David G. Campbell Carol MacKintosh Rainer Lehmann Hans-Ulrich Haering Erwin D. Schleicher Cora Weigert

Phosphorylation of insulin receptor substrate (IRS)-2 on tyrosine residues is a key event in IGF-1/insulin signaling and leads to activation of the PI 3-kinase and the Ras/MAPK pathway. Furthermore, phosphorylated serine/threonine residues on IRS-2 can induce 14-3-3 binding. In this study we searched IRS-2 for novel phosphorylation sites and investigated the interaction between IRS-2 and 14-3-3...

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