Extracellular signal-regulated kinase involvement in human astrocyte migration

Brain Research

Volumn 1164, Issue 1, 2007, Pages 1-13

  Lim, Joanne H ^a   Gibbons, Hannah M ^a   O'Carroll, Simon J ^a   Narayan, Pritika J ^a   Faull, Richard L M ^a   Dragunow, Michael ^a  

^a THE UNIVERSITY OF AUCKLAND   (New Zealand)

Author keywords

Astrocyte; Glial scar

Indexed keywords

1,4 DIAMINO 1,4 BIS(2 AMINOPHENYLTHIO) 2,3 DICYANOBUTADIENE; MITOGEN ACTIVATED PROTEIN KINASE 1;

ARTICLE; ASTROCYTE; CELL MIGRATION; CELL PROLIFERATION; CONTROLLED STUDY; DRUG INHIBITION; EMBRYO; ENZYME ACTIVATION; ENZYME PHOSPHORYLATION; HUMAN; HUMAN CELL; IMMUNOCYTOCHEMISTRY; IN VITRO STUDY; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; STEM CELL; WOUND;

ASTROCYTES; BRAIN INJURIES; CELL LINE, TUMOR; CELL MOVEMENT; CELL PROLIFERATION; CICATRIX; ENZYME ACTIVATION; ENZYME INHIBITORS; EXTRACELLULAR SIGNAL-REGULATED MAP KINASES; GLIOSIS; HUMANS; MAP KINASE SIGNALING SYSTEM; NERVE REGENERATION; PHOSPHORYLATION;

EID: 34547555822     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2007.06.020     Document Type: Article

References (53)

1. Alonso G. NG2 proteoglycan-expressing cells of the adult rat brain: possible involvement in the formation of glial scar astrocytes following stab wound. Glia 49 3 (2005) 318-338
2. Andrews P.W. Retinoic acid induces neuronal differentiation of a cloned human embryonal carcinoma cell line in vitro. Dev. Biol. 103 2 (1984) 285-293
3. Andrews P.W., Damjanov I., Simon D., Banting G.S., Carlin C., Dracopoli N.C., and Fogh J. Pluripotent embryonal carcinoma clones derived from the human teratocarcinoma cell line Tera-2. Differentiation in vivo and in vitro. Lab. Invest. 50 2 (1984) 147-162
4. Bani-Yaghoub M., Felker J.M., and Naus C.C. Human NT2/D1 cells differentiate into functional astrocytes. NeuroReport 10 18 (1999) 3843-3846
5. Beach T.G., Walker R., and McGeer E.G. Patterns of gliosis in Alzheimer's disease and aging cerebrum. Glia 2 6 (1989) 420-436
6. Carbonell W.S., and Mandell J.W. Transient neuronal but persistent astroglial activation of ERK/MAP kinase after focal brain injury in mice. J. Neurotrauma 20 4 (2003) 327-336
7. Colodner K.J., Montana R.A., Anthony D.C., Folkerth R.D., DeGirolami U., and Feany M.B. Proliferative potential of human astrocytes. J. Neuropathol. Exp. Neurol. 64 2 (2005) 163-169
8. de la Monte S.M., Ho D.D., Schooley R.T., Hirsch M.S., and Richardson Jr. E.P. Subacute encephalomyelitis of AIDS and its relation to HTLV-III infection. Neurology 37 4 (1987) 562-569
9. Delacourte A. General and dramatic glial reaction in Alzheimer brains. Neurology 40 1 (1990) 33-37
10. Di Giovanni S., Movsesyan V., Ahmed F., Cernak I., Schinelli S., Stoica B., and Faden A.I. Cell cycle inhibition provides neuroprotection and reduces glial proliferation and scar formation after traumatic brain injury. Proc. Natl. Acad Sci. U. S. A. 102 23 (2005) 8333-8338
11. Eddleston M., and Mucke L. Molecular profile of reactive astrocytes-implications for their role in neurologic disease. Neuroscience 54 1 (1993) 15-36
12. Eng L.F., Vanderhaeghen J.J., Bignami A., and Gerstl B. An acidic protein isolated from fibrous astrocytes. Brain Res. 28 2 (1971) 351-354
13. Entschladen F., Drell T.L.t., Lang K., Masur K., Palm D., Bastian P., Niggemann B., and Zaenker K.S. Analysis methods of human cell migration. Exp. Cell Res. 307 2 (2005) 418-426
14. Faber-Elman A., Solomon A., Abraham J.A., Marikovsky M., and Schwartz M. Involvement of wound-associated factors in rat brain astrocyte migratory response to axonal injury: in vitro simulation. Journal of Clinical Investigation 97 1 (1996) 162-171
15. Favata M.F., Horiuchi K.Y., Manos E.J., Daulerio A.J., Stradley D.A., Feeser W.S., Van Dyk D.E., Pitts W.J., Earl R.A., and Hobbs F. Identification of a novel inhibitor of mitogen-activated protein kinase kinase. J. Biol. Chem. 273 29 (1998) 18623-18632
16. Franco S.J., and Huttenlocher A. Regulating cell migration: calpains make the cut. J. Cell Sci. 118 Pt 17 (2005) 3829-3838
17. Ghirnikar R.S., Lee Y.L., and Eng L.F. Inflammation in traumatic brain injury: role of cytokines and chemokines. Neurochem. Res. 23 3 (1998) 329-340
18. Goldman J.E., Schaumburg H.H., and Norton W.T. Isolation and characterization of glial filaments from human brain. J. Cell Biol. 78 2 (1978) 426-440
19. Hatten M.E., Liem R.K., Shelanski M.L., and Mason C.A. Astroglia in CNS injury. Glia 4 2 (1991) 233-243
20. Holley J.E., Gveric D., Newcombe J., Cuzner M.L., and Gutowski N.J. Astrocyte characterization in the multiple sclerosis glial scar. Neuropathol. Appl. Neurobiol. 29 5 (2003) 434-444
21. Huang C., Jacobson K., and Schaller M.D. MAP kinases and cell migration. J. Cell Sci. 117 Pt. 20 (2004) 4619-4628
22. Klemke R.L., Cai S., Giannini A.L., Gallagher P.J., de Lanerolle P., and Cheresh D.A. Regulation of cell motility by mitogen-activated protein kinase. J. Cell Biol. 137 2 (1997) 481-492
23. Kornyei Z., Czirok A., Vicsek T., and Madarasz E. Proliferative and migratory responses of astrocytes to in vitro injury. J. Neurosci. Res. 61 4 (2000) 421-429
24. Lind C.R., Gray C.W., Pearson A.G., Cameron R.E., O'Carroll S.J., Narayan P.J., Lim J., and Dragunow M. The mitogen-activated/extracellular signal-regulated kinase kinase 1/2 inhibitor U0126 induces glial fibrillary acidic protein expression and reduces the proliferation and migration of C6 glioma cells. Neuroscience 141 4 (2006) 1925-1933
25. Mandell J.W., and VandenBerg S.R. ERK/MAP kinase is chronically activated in human reactive astrocytes. NeuroReport 10 17 (1999) 3567-3572
26. Mandell J.W., Gocan N.C., and Vandenberg S.R. Mechanical trauma induces rapid astroglial activation of ERK/MAP kinase: Evidence for a paracrine signal. Glia 34 4 (2001) 283-295
27. Miller R.H., and Raff M.C. Fibrous and protoplasmic astrocytes are biochemically and developmentally distinct. J. Neurosci. 4 2 (1984) 585-592
28. Mori T., Wang X., Jung J.C., Sumii T., Singhal A.B., Fini M.E., Dixon C.E., Alessandrini A., and Lo E.H. Mitogen-activated protein kinase inhibition in traumatic brain injury: in vitro and in vivo effects. J. Cereb. Blood Flow Metab. 22 4 (2002) 444-452
29. Namura S., Iihara K., Takami S., Nagata I., Kikuchi H., Matsushita K., Moskowitz M.A., Bonventre J.V., and Alessandrini A. Intravenous administration of MEK inhibitor U0126 affords brain protection against forebrain ischemia and focal cerebral ischemia. Proc. Natl. Acad Sci. U. S. A. 98 20 (2001) 11569-11574
30. Neary J.T., Kang Y., Willoughby K.A., and Ellis E.F. Activation of extracellular signal-regulated kinase by stretch-induced injury in astrocytes involves extracellular ATP and P2 purinergic receptors. J. Neurosci. 23 6 (2003) 2348-2356
31. Norenberg M.D., and Martinez-Hernandez A. Fine structural localization of glutamine synthetase in astrocytes of rat brain. Brain Res. 161 2 (1979) 303-310
32. Norton W.T., Aquino D.A., Hozumi I., Chiu F.C., and Brosnan C.F. Quantitative aspects of reactive gliosis: a review. Neurochem. Res. 17 9 (1992) 877-885
33. Norton W.T., Aquino D.A., Hozumi I., Chiu F.C., and Brosnan C.F. Quantitative aspects of reactive gliosis: a review. Neurochem. Res. 17 9 (1992) 877-885
34. Oberheim N.A., Wang X., Goldman S., and Nedergaard M. Astrocytic complexity distinguishes the human brain. Trends Neurosci. 29 10 (2006) 547-553
35. Ong W.Y., Garey L.J., and Reynolds R. Distribution of glial fibrillary acidic protein and glutamine synthetase in human cerebral cortical astrocytes-a light and electron microscopic study. J. Neurocytol. 22 10 (1993) 893-902
36. Pearson G., Robinson F., BeersGibson T., Xu B.E., Karandikar M., Berman K., and Cobb M.H. Mitogen-activated protein (MAP) kinase pathways: regulation and physiological functions. Endocr. Rev. 22 2 (2001) 153-183
37. Pekny M., and Nilsson M. Astrocyte activation and reactive gliosis. Glia 50 4 (2005) 427-434
38. Pleasure S.J., Page C., and Lee V.M. Pure, postmitotic, polarized human neurons derived from NTera 2 cells provide a system for expressing exogenous proteins in terminally differentiated neurons. J. Neurosci. 12 5 (1992) 1802-1815
39. Reddy K.B., Nabha S.M., and Atanaskova N. Role of MAP kinase in tumor progression and invasion. Cancer Metastasis Rev. 22 4 (2003) 395-403
40. Roux P.P., and Blenis J. ERK and p38 MAPK-activated protein kinases: a family of protein kinases with diverse biological functions. Microbiol. Mol. Biol. Rev. 68 2 (2004) 320-344
41. Rutka J.T., Murakami M., Dirks P.B., Hubbard S.L., Becker L.E., Fukuyama K., Jung S., Tsugu A., and Matsuzawa K. Role of glial filaments in cells and tumors of glial origin: a review. J. Neurosurg. 87 3 (1997) 420-430
42. Sandhu J.K., Sikorska M., and Walker P.R. Characterization of astrocytes derived from human NTera-2/D1 embryonal carcinoma cells. J. Neurosci. Res. 68 5 (2002) 604-614
43. Silver J., and Miller J.H. Regeneration beyond the glial scar. Nat. Rev., Neurosci. 5 2 (2004) 146-156
44. Vis J.C., Nicholson L.F., Faull R.L., Evans W.H., Severs N.J., and Green C.R. Connexin expression in Huntington's diseased human brain. Cell Biol. Int. 22 11-12 (1998) 837-847
45. Walz W., and Lang M.K. Immunocytochemical evidence for a distinct GFAP-negative subpopulation of astrocytes in the adult rat hippocampus. Neurosci. Lett. 257 3 (1998) 127-130
46. Wang X., Wang H., Xu L., Rozanski D.J., Sugawara T., Chan P.H., Trzaskos J.M., and Feuerstein G.Z. Significant neuroprotection against ischemic brain injury by inhibition of the MEK1 protein kinase in mice: exploration of potential mechanism associated with apoptosis. J. Pharmacol. Exp. Ther. 304 1 (2003) 172-178
47. Wang M., Kong Q., Gonzalez F.A., Sun G., Erb L., Seye C., and Weisman G.A. P2Y nucleotide receptor interaction with alpha integrin mediates astrocyte migration. J. Neurochem. 95 3 (2005) 630-640
48. Webb D.J., Donais K., Whitmore L.A., Thomas S.M., Turner C.E., Parsons J.T., and Horwitz A.F. FAK-Src signalling through paxillin, ERK and MLCK regulates adhesion disassembly. Nat. Cell Biol. 6 2 (2004) 154-161
49. Webster B., Hansen L., Adame A., Crews L., Torrance M., Thal L., and Masliah E. Astroglial activation of extracellular-regulated kinase in early stages of Alzheimer disease. J. Neuropathol. Exp. Neurol. 65 2 (2006) 142-151
50. Wu V.W., and Schwartz J.P. Cell culture models for reactive gliosis: new perspectives. J. Neurosci. Res. 51 6 (1998) 675-681
51. Yu A.C., Lee Y.L., and Eng L.F. Astrogliosis in culture: I. The model and the effect of antisense oligonucleotides on glial fibrillary acidic protein synthesis. J. Neurosci. Res. 34 3 (1993) 295-303
52. Zhao M.L., Liu J.S., He D., Dickson D.W., and Lee S.C. Inducible nitric oxide synthase expression is selectively induced in astrocytes isolated from adult human brain. Brain Res. 813 2 (1998) 402-405
53. Zlotnik I. The reaction of astrocytes to acute virus infections of the central nervous system. Br. J. Exp. Pathol. 49 6 (1968) 555-564