Literature DB >> 1384043

Activation of phosphatidylinositol 3-kinase by epidermal growth factor, basic fibroblast growth factor, and nerve growth factor in PC12 pheochromocytoma cells.

S Raffioni1, R A Bradshaw.   

Abstract

Epidermal growth factor (EGF), basic fibroblast growth factor (bFGF), and nerve growth factor (NGF), which stimulate the phosphorylation of proteins on tyrosine in PC12 cells, initiate these modifications through ligand-specific cell surface receptors that contain the causative tyrosine kinases. One apparent substrate for these enzymes is phosphatidylinositol 3-kinase (PI 3-kinase), an enzyme that phosphorylates the D-3 position of the inositol ring and associates with several protein tyrosine kinases, as indicated by the fact that it is immunoprecipitated from EGF-, bFGF-, and NGF-stimulated PC12 cells by an anti-phosphotyrosine antibody. All three growth factors increase immunoprecipitable PI 3-kinase activity after 2 min of addition at concentrations able to stimulate either mitogenic or neurotrophic responses in PC12 cells. The level of stimulation of PI 3-kinase activity by EGF, bFGF, and NGF is 15- to 20-fold, 2- to 3-fold, and 8- to 10-fold, respectively. Moreover, tyrosine phosphorylation of PI 3-kinase was detected in EGF-, bFGF-, and NGF-stimulated PC12 cells, and the amount of the phosphorylation correlated with the level of stimulation of enzyme activity. In contrast, phosphatidylinositol 4-kinase, which produces the inositol phospholipids cleaved by phospholipase C-gamma to yield diacylglycerol and inositol-1,4,5-trisphosphate, is not affected by these growth factors. The pattern of stimulation of PI 3-kinase does not correlate with the induction of neurite outgrowth but rather with the mitotic responses, suggesting that PI 3-kinase and its products may be more important for signaling in cell division than in trophic processes. However, the levels of phosphatidylinositol 3-phosphate do not coincide with the stimulation of [3H]thymidine incorporation by these growth factors, rendering its role in mitotic functions, at least in PC12 cells, also uncertain.

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Year:  1992        PMID: 1384043      PMCID: PMC50077          DOI: 10.1073/pnas.89.19.9121

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  36 in total

1.  Phosphatidylinositol kinase type I activity associates with various oncogene products.

Authors:  Y Fukui; S Kornbluth; S M Jong; L H Wang; H Hanafusa
Journal:  Oncogene Res       Date:  1989

2.  Role of phosphatidylinositol kinase in PDGF receptor signal transduction.

Authors:  S R Coughlin; J A Escobedo; L T Williams
Journal:  Science       Date:  1989-03-03       Impact factor: 47.728

3.  PDGF-dependent tyrosine phosphorylation stimulates production of novel polyphosphoinositides in intact cells.

Authors:  K R Auger; L A Serunian; S P Soltoff; P Libby; L C Cantley
Journal:  Cell       Date:  1989-04-07       Impact factor: 41.582

4.  Association of phosphatidylinositol kinase activity with polyoma middle-T competent for transformation.

Authors:  M Whitman; D R Kaplan; B Schaffhausen; L Cantley; T M Roberts
Journal:  Nature       Date:  1985 May 16-22       Impact factor: 49.962

5.  Nerve growth factor-treated, neurite-bearing PC12 cells continue to synthesize DNA.

Authors:  M J Ignatius; C R Chandler; E M Shooter
Journal:  J Neurosci       Date:  1985-02       Impact factor: 6.167

6.  Evidence that the Rous sarcoma virus transforming gene product phosphorylates phosphatidylinositol and diacylglycerol.

Authors:  Y Sugimoto; M Whitman; L C Cantley; R L Erikson
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

7.  Production of 1,2-diacylglycerol in PC12 cells by nerve growth factor and basic fibroblast growth factor.

Authors:  J G Altin; R A Bradshaw
Journal:  J Neurochem       Date:  1990-05       Impact factor: 5.372

8.  Production, biological activity, and structure of recombinant basic fibroblast growth factor and an analog with cysteine replaced by serine.

Authors:  G M Fox; S G Schiffer; M F Rohde; L B Tsai; A R Banks; T Arakawa
Journal:  J Biol Chem       Date:  1988-12-05       Impact factor: 5.157

9.  Cell cycle-specific action of nerve growth factor in PC12 cells: differentiation without proliferation.

Authors:  B B Rudkin; P Lazarovici; B Z Levi; Y Abe; K Fujita; G Guroff
Journal:  EMBO J       Date:  1989-11       Impact factor: 11.598

10.  Nerve growth factor-induced alteration in the response of PC12 pheochromocytoma cells to epidermal growth factor.

Authors:  K Huff; D End; G Guroff
Journal:  J Cell Biol       Date:  1981-01       Impact factor: 10.539

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  29 in total

1.  Phosphatidylinositol 3-kinase and Akt protein kinase are necessary and sufficient for the survival of nerve growth factor-dependent sympathetic neurons.

Authors:  R J Crowder; R S Freeman
Journal:  J Neurosci       Date:  1998-04-15       Impact factor: 6.167

2.  Nerve growth factor activation of the extracellular signal-regulated kinase pathway is modulated by Ca(2+) and calmodulin.

Authors:  J Egea; C Espinet; R M Soler; S Peiró; N Rocamora; J X Comella
Journal:  Mol Cell Biol       Date:  2000-03       Impact factor: 4.272

3.  Class II phosphoinositide 3-kinases are downstream targets of activated polypeptide growth factor receptors.

Authors:  A Arcaro; M J Zvelebil; C Wallasch; A Ullrich; M D Waterfield; J Domin
Journal:  Mol Cell Biol       Date:  2000-06       Impact factor: 4.272

4.  Stimulation of C2C12 myoblast growth by basic fibroblast growth factor and insulin-like growth factor 1 can occur via mitogen-activated protein kinase-dependent and -independent pathways.

Authors:  D J Milasincic; M R Calera; S R Farmer; P F Pilch
Journal:  Mol Cell Biol       Date:  1996-11       Impact factor: 4.272

5.  Mitogenic signals and transforming potential of Nyk, a newly identified neural cell adhesion molecule-related receptor tyrosine kinase.

Authors:  L Ling; H J Kung
Journal:  Mol Cell Biol       Date:  1995-12       Impact factor: 4.272

6.  The phosphatidylinositol 3-kinase alpha is required for DNA synthesis induced by some, but not all, growth factors.

Authors:  S Roche; M Koegl; S A Courtneidge
Journal:  Proc Natl Acad Sci U S A       Date:  1994-09-13       Impact factor: 11.205

7.  Threshold levels of ERK activation for chemotactic migration differ for NGF and EGF in rat pheochromocytoma PC12 cells.

Authors:  W C Ho; S Uniyal; H Zhou; V L Morris; B M C Chan
Journal:  Mol Cell Biochem       Date:  2005-03       Impact factor: 3.396

8.  Targeted approach to metastatic colorectal cancer: what comes beyond epidermal growth factor receptor antibodies and bevacizumab?

Authors:  Teresa Troiani; Erika Martinelli; Floriana Morgillo; Anna Capasso; Anna Nappi; Vincenzo Sforza; Fortunato Ciardiello
Journal:  Ther Adv Med Oncol       Date:  2013-01       Impact factor: 8.168

9.  Divergence in signaling pathways involved in promotion of cell viability mediated by bFGF, NGF, and EGF in PC12 cells.

Authors:  Takakazu Kawamata; Tomoko Yamaguchi; Kazuo Shin-ya; Tomokatsu Hori
Journal:  Neurochem Res       Date:  2003-08       Impact factor: 3.996

10.  Regeneration of diabetic axons is enhanced by selective knockdown of the PTEN gene.

Authors:  Bhagat Singh; Vandana Singh; Anand Krishnan; Kurien Koshy; Jose A Martinez; Chu Cheng; Chris Almquist; Douglas W Zochodne
Journal:  Brain       Date:  2014-02-27       Impact factor: 13.501

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