Physiological levels of β-amyloid peptide stimulate protein kinase C in PC12 cells

Brain Research

Volumn 769, Issue 2, 1997, Pages 287-295

  Luo, Y ^a   Hawver, D B ^a   Iwasaki, K ^b   Sunderland, T ^b   Roth, G S ^a   Wolozin, B ^c  

^a NATIONAL INSTITUTE ON AGING   (United States)

^b NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^c LOYOLA UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Alzheimer's disease; Protein kinase C; Signal transduction

Indexed keywords

AMYLOID BETA PROTEIN; PROTEIN KINASE C; PROTEIN SERINE THREONINE KINASE;

ALZHEIMER DISEASE; ANIMAL CELL; ARTICLE; ENZYME ACTIVATION; ENZYME ACTIVITY; ENZYME REGULATION; NONHUMAN; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN PHOSPHORYLATION; RAT; SIGNAL TRANSDUCTION;

AMYLOID BETA-PROTEIN; ANIMALS; BIOLOGICAL TRANSPORT; HUMANS; ISOENZYMES; PC12 CELLS; PROTEIN KINASE C; PROTEIN KINASE C-ALPHA; PROTEIN-SERINE-THREONINE KINASES; RATS;

EID: 0030730529     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(97)00718-X     Document Type: Article

References (50)

1. Akimoto K., Takahashi R., Moriya S., Nishioka N., Takayanagi J., Kimura K., Fukui Y., Osada S., Mizuno K., Hirai S., Kazlauskas A., Ohno S. EGF or PDGF receptors activate atypical PKCα through phosphatidylinositol 3-kinase. EMBO J. 15:1996;788-798.
2. Chauhan A., Chauhan V., Murakami N., Brockerhoff H., Wisniewski H. Amyloid β-protein stimulates casein kinase I and casein kinase II activities. Brain Res. 629:1993;47-52.
3. Chauhan A., Chauhan V., Brockerhoff H., Wisniewski H. Action of amyloid beta-protein on protein kinase C activity. Life Sci. 49:1991;1555-1562.
4. Chauhan A., Chauhan V., Singh S., Brockerhoff H., Wisniewski H. Stimulation of phosphatidylinositol 3-kinase activity by Alzheimer's amyloid beta-protein. J. Neurochem. 65:1995;S45.
5. Chen M., Yankner B. An antibody to β amyloid and the amyloid precusor protein inhibits cell-substratum adhesion in many mammalian cell types. Neurosci. Lett. 125:1991;223-226.
6. Clark E., Leach K., Trojanowski J., Lee V. Characterization and differential distribution of the three major human protein kinase C isozymes (PKCα, PKCβ, and PKCγ) of the central nervous system in normal and Alzheimer's disease brain. Lab. Invest. 64:1991;35-44.
7. Cole G., Dobkins K., Hansen L., Terry R., Saitoh T. Decreased levels of protein kinase C in Alzheimer brain. Brain Res. 452:1988;165-174.
8. Coleman E., Wooten M. Nerve growth factor-induced differentiation of PC12 cells employs the PMA-insensitive protein kinase C-ζ isoform. J. Mol. Neurosci. 5:1994;39-57.
9. Ettinger S., Lauener R., Duronio V. Protein kinase C δ specifically associates with phosphatidylinositol 3-kinase following cytokine stimulation. J. Biol. Chem. 271:1996;14514-14518.
10. s6k. Crit. Rev. Biochem. Mol. Biol. 29:1994;385-413.
11. Ghiso J., Rostagno A., Gardella J., Liem L., Gorevic P., Frangione B. A 109-amino-acid C-terminal fragment of Alzheimer's disease amyloid precursor protein contains a sequence, -RHDS-, that promotes cell adhesion. Biochem. J. 288:1992;1053-1059.
12. Gomez J., Martinez C., Garcia A., Rebollo A. Association of phosphatidylinositol 3 kinase to protein kinase ζ during interleukin-2 stimulation. Eur. J. Immunol. 26:1996;1781-1787.
13. Guroff G. Nerve growth factor as a neurotrophic agent. Ann. NY Acad. Sci. 692:1993;51-59.
14. Haass C., Schlossmacher M., Hung A., Vigo-Pelfry C., Mellon A., Ostaszewski B., Lieberburg I., Koo E., Schenk D., Teplow D., Selkoe D. Amyloid β-peptide is produced by cultured cells during normal metabolism. Nature. 359:1992;322-324.
15. Hogan M., Pawlowska Z., Yang H.-A., Kornecki E., Ehrlich Y. Surface phosphorylation by ecto-protein kinase C in brain neurons: a target for Alzheimer's β-amyloid peptides. J. Neurochem. 65:1995;2022-2030.
16. House C., Kemp B. Protein kinase C contains a pseudosubstrate prototope in its regulatory domain. Science. 238:1987;1726-1728.
17. Huang K.-P., Huang F. How is protein kinase C activated in CNS? Neurochem. Int. 22:1993;417-433.
18. Hundle B., McMahon T., Dadgar J., Messing R. Overexpression of ε-protein kinase C enhances nerve growth factor-induced phosphorylation of mitogen-activated protein kinase and neurite outgrowth. J. Biol. Chem. 270:1995;30134-30140.
19. Kang J., Lamaire H., Unterbeck A., Salbaum J., Masters C., Grzeschik K., Multhaup G., Beyreuther K., Muller-Hill B. The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor. Nature. 325:1987;733-736.
20. Kapeller R., Cantley L. Phosphatidylinositol 3-kinase. BioEssays. 16:1994;565-576.
21. 1 cells. Mol. Endocrinol. 4:1990;59-68.
22. Kishimoto A., Mikawa K., Hashimoto K., Yasuda I., Tanaka S., Tominaga M., Kuroda T., Nishizuka N. Limited proteolysis of protein kinase C subspecies by calcium-dependent neutral protease (calpain). J. Biol. Chem. 264:1989;4088-4092.
23. Klegeris A., Walker D., McGeer P. Interaction of Alzheimer β-amyloid peptide with the human monocytic cell line THP-1 results in a protein kinase C-dependent secretion of tumor necrosis factor-α Brain Res. 747:1997;114-121.
24. Luo Y., Hirashima N., Li Y., Alkon D., Sunderland T., Etcheberrigaray R., Wolozin B. Physiological levels of β-amyloid increase tyrosine phosphorylation and cytosolic calcium. Brain Res. 681:1995;65-74.
25. Luo Y., Sunderland T., Roth G., Wolozin B. Physiological levels of β-amyloid peptide promote PC12 cell proliferation. Neurosci. Lett. 217:1996;125-128.
26. Luo Y., Sunderland T., Wolozin B. Physiological levels of β-amyloid activate PI3-kinase with the involvement of tyrosine phosphorylation. J. Neurochem. 67:1996;978-987.
27. Maher P. Nerve growth factor induces protein-tyrosine phosphorylation. Proc. Natl. Acad. Sci. USA. 85:1988;6788-6791.
28. Masliah E., Cole G., Hansen L., Mallory M., Albright T., Terry R., Saitoh T. Protein kinase C alteration is an early biochemical marker in Alzheimer's disease. J. Neurosci. 11:1991;2761-2767.
29. Masliah E., Cole G., Shimohama S., Hansen L., DeTeresa R., Terry R., Saitoh T. Differential involvement of protein kinase C isozymes in Alzheimer's disease. J. Neurosci. 10:1990;2113-2124.
30. 2+-independent protein kinase C changes in the brains of patients with Alzheimer's disease. J. Neurochem. 67:1996;317-323.
31. Meyer T., Regenass U., Fabbro D., Alteri E., Rösel J., Müller M., Caravatti G., Matter A. A Derivative of staurosporine (CGP 41 251) shows selectivity for protein kinase C inhibition and in vitro anti-proliferative as well as in vivo anti-tumor activity. Int. J. Cancer. 43:1989;851-856.
32. Mosthaf L., Kellerer M., Muhlhofer A., Mushack J., Seffer E., Haring H. Insulin leads to a parallel translocation of PI-3-kinase and protein kinase C ζ Exp. Clin. Endocrinol. Diabetes. 104:1996;19-24.
33. Nishizuka Y. The molecular heterogeneity of protein kinase C and its implications for cellular regulation. Nature. 334:1988;661-665.
34. O'Driscoll K., Teng K., Fabbro D., Greene L., Weinstein I. Selective translocation of protein kinase C-δ in PC12 cells during nerve growth factor-induced neuritogenesis. Mol. Biol. Cell. 6:1995;449-458.
35. Ohmichi M., Zhu G., Saltiel A. Nerve growth factor activates calcium-insensitive protein kinase C-ε in PC-12 rat pheochromocytoma cells. Biochem. J. 295:1993;767-772.
36. Selkoe D. Normal and abnormal biology of the β-amyloid precursor protein. Annu. Rev. Neurosci. 17:1994;489-517.
37. Seubert P., Vigo-Pelfrey C., Esch F., Lee M., Dovey H., Davis D., Sinha S., Schlossmacher M., Whaley J., Swindlehurst C., McCormack R., Wolfert R., Selkoe D., Lieberburg I., Schenk D. Isolation and quantification of soluble Alzheimer's β-peptide from biological fluids. Nature. 359:1992;325-327.
38. Shea T., Cressman C., Spencer M., Beermann M., Nixon R. Enhancement of neurite outgrowth following calpain inhibition is mediated by protein kinase C. J. Neurochem. 65:1995;517-527.
39. Singh K., Taylor L., Campbell X., Fields A., Neet K. A bryostatin-sensitive protein kinase C required for nerve growth factor activity. Biochemistry. 33:1994;542-551.
40. Singh V., Cheng J.-F., Leu S. Effects of substance P and protein kinase inhibitors on β-amyloid peptide-induced proliferation of cultured brain cells. Brain Res. 660:1994;353-356.
41. Ueda K., Yagami T., Kageyama H., Kawasaki K. Protein kinase inhibitor attenuates apoptotic cell death induced by amyloid beta protein in culture of the rat cerebral cortex. Neurosci. Lett. 203:1996;175-178.
42. Vigo-Pelfrey C., Lee D., Keim P., Lieberburg I., Schenk D. Characterization of β-amyloid peptide from human cerebrospinal fluid. J. Neurochem. 61:1993;1965-1968.
43. Wang H.-Y., Pisano M., Friedman E. Attenuated protein kinase C activity and translocation in Alzheimer's disease brain. Neurobiol. Aging. 15:1994;293-298.
44. Whitson J., Glabe C., Shintani E., Abcar A., Cotman C. β-Amyloid protein promotes neuritic branching in hippocampal cultures. Neurosci. Lett. 110:1990;319-324.
45. Whitson J., Selkoe D., Cotman C. Amyloid β protein enhances the survival of hippocampal neurons in vitro. Science. 243:1989;1488-1490.
46. Yankner B.A., Duffy L.K., Kirschner D.A. Neurotrophic and neurotoxic effects of amyloid β protein: reversal by tachykinin neuropeptides. Science. 250:1990;279-282.
47. Young S., Rothbard J., Parker P. A monoclonal antibody recognising the site of limited proteolysis of protein kinase C: inhibition of down-regulation in vivo. Eur. J. Biochem. 173:1988;247-252.
48. Zhang C., Lambert M., Bunch C., Barber K., Wade W., Krafft G., Klein W. Focal adhesion kinase expressed by nerve cell lines shows increased tyrosine phosphorylation in response to Alzheimer's Aβ peptide. J. Biol. Chem. 269:1994;25247-25250.
49. Zhang C., Qiu H., Krafft G., Klein W. Protein kinase C and F-actin are essential for stimulation of neuronal FAK tyrosine phosphorylation by G-proteins and amyloid beta protein. FEBS Lett. 386:1996;185-188.
50. Zheng W.-H., Fink D., Guroff G. Role of protein kinase Cα in nerve growth factor-induced arachidonic acid release from PC12 cells. J. Neurochem. 66:1996;1868-1875.