Tenascin-C mRNA and Tenascin-C Protein Immunoreactivity Increase in Astrocytes after Activation by bFGF

References

• Aloisi F, Borsellino G., Samoggia P., Test U., Chelucci C., Russo G., Peschle C., Levi G. “Astrocytes cultures from human embryonic brain: characterization and modulation of surface molecules by inflammatory cytokines”. J. Neurosci. Res. 1992; 3: 494–506
   Web of Science ®Google Scholar
• Baird A. “Fibroblast growth factors; activities and signifi cance of non-neurotrophin neurotrophic growth factors”. Curr. Opin. Neurobiol 1994; 4: 78–86
   PubMedGoogle Scholar
• Bartsch S, Bartsch U., Dörries U., Faissner A., Weller A., Ekblom P., Schachner M. “Expression of tenascin in the developing and adult cerebellar cortex”. J. Neuroscience. 1992a; 12: 736–749
   PubMed Web of Science ®Google Scholar
• Bansch U, Bartsch S., Dörries U., Schachner M. “Immunological localization of tenascin in the developing and lesioned adult mouse optic nerve”. European. J. Neurosci. 1992b; 4: 338–352
   PubMed Web of Science ®Google Scholar
• Beach T G, Walker R., McGeer E. G. “Patterns of gliosis in Alzheimer's disease and aging cerebrum”. Glia. 1989; 2: 420–436
   PubMed Web of Science ®Google Scholar
• Borsi L., Carnemolla B., Nicolo G., Spina B., Tanara G., Zardi L. Expression of different tenascin isoorms in normal hyperplastic and neoplastic human breast tissues. Int. J. Cancer 1992; 52: 688–692
   PubMed Web of Science ®Google Scholar
• Borsi L, Balza E., Castellani P., Carmonella B., Ponassi M., Querzé G., Zardi L. “Cell-cycle dependent alter native splicing of the tenascin primary transcript”. Cell. Adhe sion. Comm. 1994a; 1: 307–317
   Web of Science ®Google Scholar
• Borsi L, Balza E., Gaggero B., Allemanni Zardi G. “The alternative splicing pattern of the tenascin-C pre-mRNA is controlled by the extracellular pH”. The Journal of Biol. Chem. 1995b; 270(11)6243–6245
   PubMed Web of Science ®Google Scholar
• Breen K C. “The developmental regulation of the L2 and carbohydrate epitopes in mouse brain: evidence for separate control of lipid-and protein bound epitopes”. FEBS Lett. 1989; 247: 36–40
   PubMed Web of Science ®Google Scholar
• Bugra K, Pollard H., Charton G., Moreau J., Ben-Ari Y., Khrestchatisky M. “aFGF, bFGF and flg mRNAs show distinct patterns of induction in the hippocampus following kainate-induced seizures”. European. J. Neurosci. 1994; 6: 58–66
   PubMed Web of Science ®Google Scholar
• Caday C G, Klagsbrun M., Fanning P. J., Mirzabegian A., Finklestein S. P. “Fibroblast growth factor (FGF) levels in the developing rat brain”. Dev. Brain. Res. 1990; 52: 241–246
   PubMedGoogle Scholar
• Chomczynski P, Sacchi N. “Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform ex traction”. Analytical Biochem. 1987; 162: 156–159
   PubMed Web of Science ®Google Scholar
• Chuong C M, Crossin K. L., Edelman G. M. “Sequen tial expression and differential function of multiple adhesion molecules during the formation of cerebellar cortical layers”. J. Cell Biol. 1987; 104: 331–342
   PubMed Web of Science ®Google Scholar
• Dahl D, Bignami A. “Heterogeneity of the glial fibrillary acidic protein in gliosed human brain”. J. Neurol Sci. 1974; 23: 551–563
   PubMed Web of Science ®Google Scholar
• Davis J B, Stoobant P. “Platelet-derived growth factors and fibroblast growth factors are mitogens for rat Schwann cells”. J. Cell. Biol. 1990; 110: 1353–1360
   PubMed Web of Science ®Google Scholar
• De la Monte S M, Ho D., Schooley R. T., Hrsch M. S., Rich ardson E. P., Jr. “Subacute encephalomyelitis of AIDS and its relation to HTLV-ffl infection”. Neurology 1987; 37: 562–659
   PubMed Web of Science ®Google Scholar
• Eccleston A, Silberberg D. R. “Fibroblast growth factor is a mitogen for oligodendrocytes in vitro”. Dev. Brain. Res. 1985; 21: 315–318
   Google Scholar
• Eddleston M, Mucke L. “Molecular profile of reactive astrocytes-implications for their role in neurologic disease”. Neuroscience. 1993; 54: 15–36
   PubMed Web of Science ®Google Scholar
• Edelman G M. “Cell adhesion molecules in neuronal histogenesis”. Annu. Rev. Physiol. 1986; 48: 417–430
   PubMed Web of Science ®Google Scholar
• Emoto N, Gonzalez A., Walicke P. A., Wada E., Simmons D. M., Shimakasi S., Baird A. “Basic fibroblast growth factor (FGF) in the central nervous system: identification of spe cific loci of basic FGF expression in the rat brain”. Growth Factors. 1989; 2: 21–29
   PubMed Web of Science ®Google Scholar
• Erickson H P. “Tenascin-C, tenascin-R, and tenascin X, a family of talented proteins in search of a function”. Curr. Opin ion. Cell. Biol. 1993; 5: 869–876
   PubMed Web of Science ®Google Scholar
• Faissner A, Kruse J. “J1/Tenascin is a repulsive substrate for central nervous system neurons”. Neuron. 1990; 5: 627–637
   PubMed Web of Science ®Google Scholar
• Faissner A, Götz B., Joester A., Schoze A. “The tenascin gene family-versatile glycoproteins implicated in neuronal pat tern formation and regeneration”. Dev. Biol. 1995c; 6: 139–148
   Google Scholar
• Ferhat L., Krestchatisky M., Roisin M. P., Barbin G. Basic Fibroblast growth factor-induced increase in zif/268 and c-fos mRNA levels is Ca2+ dependent in primary cultures of hippocampal neurons. J. Neurochem. 1993; 61: 1105–1112
   PubMed Web of Science ®Google Scholar
• Fehrat L, Chevassus A U, Louis N., Jorquera I., Niquet J., Khrestchatisky M., Ben-Ari Y., Represa A. “Tran sient increase of tenascin-C in immature hippocampus: astroglial and neuronal expression”. Journal of Neurocytology 1995; 25: 53–66
   Google Scholar
• Feige J-J, Bradley J. D., Fryburg K., Farris J., Cousens L. C., Barr P. J., Baird A. “Differential effects of heparin, fibronectin, and laminin on the phosphorylation of basic fibroblast growth factor by protein kinase C and the catalytic subunit of protein kinase A”. J. Cell. Biol. 1989; 109: 3105–3114
   PubMed Web of Science ®Google Scholar
• Florkiewicz R Z, Baird A., Gonzalez A. M. “Multiple forms of bFGF: differential nuclear and cell surface localiza tion”. Growth Factors. 1991; 4: 265–275
   PubMed Web of Science ®Google Scholar
• Gall C M, Berschauer R., Isacson P. J. “Seizures increase basic fibroblast growth factor mRNA in adult rat forebrain neu rons and glia”. Mol. Brain. Res. 1994; 21: 190–205
   PubMedGoogle Scholar
• Gomez-Pinilla F, Vu L., Cotman C. W. “Regulation of astrocyte proliferation by FGF-2 and Heparan sulfate in vivo”. J. Neurosci. 1995; 15: 2021–2029
   PubMed Web of Science ®Google Scholar
• Grierson J P, Petroski R. E., Ling D. S.F., Geller H. M. “Astrocyte topography and tenascin/cytotactin expression: cor relation with the ability to support neuritic outgrowth”. Dev. Brain. Res. 1990; 55: 11–19
   PubMedGoogle Scholar
• Gulcher J R, Marton Stefansson L. S. “Two large glycosylated polypeptides found in myelinating oligodendrocytes but not in myelin”. Proc, Natl. Acad. Sci. 1986a; 83: 2118–2122
   PubMed Web of Science ®Google Scholar
• Gulcher J R, Nies D. E., Marton L. S., Stefansson K. “An alternatively spliced region of the human hexabrachion con tains a repeat of potential N-glycosylation sites”. Proc. Natl. Acad. Sci. 1989b; 86: 1588–1592
   PubMed Web of Science ®Google Scholar
• Kruse J., Keilhauer G., Faissner A., Timpl R., Schachner M. “The J1 glycoproteina novel nervous system cell ad hesion molecule of the L2/HNK family”. Nature 1985; 316: 146–148
   PubMed Web of Science ®Google Scholar
• Künemund V, Jungalwala F. B., Fischer G., Chou D. K.H., Keil hauer G., Schachner M. “The L2/HNK-1 carbohy drate of neural cell adhesion molecules is involved in cell inter actions”. J Cell. Biol. 1988; 106: 213–223
   PubMed Web of Science ®Google Scholar
• Laemmeli U K. “Cleavage of structural proteins during the assembly of bacteriopphage T4”. Nature 1970; 221: 680–685
   Web of Science ®Google Scholar
• Laywell E D, Domes U., Bartsch U., Faissner A., Schachner M., Steindler D. A. “Enhanced expression of the developmentally regulated extracellular matrix molecule tenascin fol lowing adult brain injury”. Proc. Natl. Acad. Sci. 1992; 89: 2634–2638
   PubMed Web of Science ®Google Scholar
• Letoumeau P C, Condic M. L., Snow M. D. “Interac tions of developing neurons with the extracellular matrix”. J. Neuwsci. 1994; 14: 915–928
   PubMed Web of Science ®Google Scholar
• Lips K, Stichel C. C., Hans-Werner Müller. “Restricted appearance of tenascin and chondroitine sulphate proteoglycans after transection and sprouting of adult rat post-commissural fornix”. J. Neurocytology 1995; 24: 449–464
   PubMedGoogle Scholar
• Lochter A., Vaughan L., Kaplony A., Prochiantz A., Schachner M., Faissner A. J1/tenascin in substrate-bound and soluble form displays contrary effects on neurite outgrowth. J. Cell Biol. 1991; 113: 1159–1171
   PubMed Web of Science ®Google Scholar
• Lowry G H, Rosenbourg N J., Farr A. L., Randall R. J. “Protein measurement with folin reagent”. J. Biol. Chem. 1951; 193: 265–275
   PubMed Web of Science ®Google Scholar
• McKeon R J, Schreiber R C., Rudge J. S., Silver J. “Reduction of neurite outgrowth in a model of glial scarring following CNS injury is correlated with the expression of inhib itory molecules on reactives astrocytes”. J. Neurosci. 1991; 11: 3398–3411
   PubMed Web of Science ®Google Scholar
• Meiners S, Marone M., Rittenhouse J. L., Geller H. M. “Regulation of astrocytic tenascin by basic fibroblast growth factor”. Dev. Biol. 1993; 160: 480–493
   PubMed Web of Science ®Google Scholar
• Morrison D K, Kaplan D. R., Rapp U., Roberts T. M. “Signal transduction from membrane to cytoplasm: growth fac tors and membrane-bound oncogene products increase Raf-1 phosphorylation and associated protein kinase activity”. Proc. Natl. Acad. Sci. 1988b; 85: 885–8859
   PubMed Web of Science ®Google Scholar
• Morrison R S, De Vellis J., Lee Y. L., Bradshaw R. A., Eng L. F. “Hormones and growth factors induced the synthesis of glial fibrillary acidic protein in rat brain astrocytes”. J. Neurosci. Res. 1985a; 14: 167–172
   PubMed Web of Science ®Google Scholar
• Mucker L, Oldstone M. B.A., Morris J. C., Nerenberg M. I. “Rapid-activation of astrocyte-specific expression of GFAP-lacZ transgene by focal injury”. New Biol. 1991; 3: 465–474
   PubMedGoogle Scholar
• Nichols N R, Osterburg H. H., Masters J. N., Millar S. L., Finch C. E. “Messenger RNA for glial acidic protein is decreased in rat brain following acute and chronic corticosterone treatment”. Mol. Brain. Res. 1990; 1: 1–7
   Google Scholar
• Niquet J, Jorquera L., Ben-Ari Represa Y. “N-CAM immunoreactivity on mossy fibers and reactive astrocytes in the hippocampus of epileptic rats”. Brain Res. 1993; 626: 106–116
   PubMed Web of Science ®Google Scholar
• Niquet J, Ben-Ari Y., Represa A. “Glial reaction after seizure induced hippocampal lesion: immunohistochemical char acterization of proliferating glial cells”. J. Neurocvtol. 1994; 23: 641–656
   PubMedGoogle Scholar
• Niquet J., Jorquera J., Ben-Ari Y., Represa A. Proliterative astrocytes may express fibronectin-like protein in the hippocampus of epileptic rats. Neurosci Lett. 1996b; 180: 13–16
   Web of Science ®Google Scholar
• Niquet J, Jorquera I., Faissner A., Ben-Ari Y., Represa A. “Gliosis and axonal sprouting in the hippocampus of epileptic rats are associated with an increase of tenascin-C im munoreactivity”. J. Neurocytol. 1995; 24: 611–624
   PubMedGoogle Scholar
• O'Shea K S, Liu L H., Dixit V. M. “Thrombospondin and 140 kDa fragment promote adhesion and neurite outgrowth from embryonic central and peripheral neurons and from PC 12 cells”. Neuron. 1991; 7: 231–237
   PubMed Web of Science ®Google Scholar
• Perraud F, Labourdette G., Miehe M., Loret C., Sensenbrenner M. “Comparison of the morphological effects of acidic and basic fibroblast growth factors on rat astroblasts in culture”. J. Neurosci. Res. 1988a; 20: 1–11
   PubMed Web of Science ®Google Scholar
• Perraud F, Labourdette G., Enclancher F., Sensenbrenner M. “Primary cultures of astrocytes from different brain ar eas of newborn rats and effects of basic fibroblast growth fac tor”. Dev. Neurosci. 1990b; 12: 11–21
   PubMed Web of Science ®Google Scholar
• Pindzola R R, Doller C., Silver J. “Putative inhibitory extracellular matrix molecules at the dorsal root entry zone of the spinal cord during development and after root and sciatic nerve lesions”. Dev. Biol. 1993; 156: 34–48
   PubMed Web of Science ®Google Scholar
• Prieto A L, Jones F S., Cunningham B. A., Crossin K. L., Edelman G. M. “Localization during development of alterna tively spliced forms of cytotactin mRNA by in situ hybridiza tion”. J. Cell. Biol. 1990; 111: 685–698
   PubMed Web of Science ®Google Scholar
• Reichardt L F, Tomaselli K. J. “Extracellular matrix molecules and their receptors: functions in neural development”. Ann. Rev. Neurosci. 1991; 14: 531–570
   PubMed Web of Science ®Google Scholar
• Represa A, Niquet J., Charriaut-Marlangue C., Ben-Ari Y. “Reactive astrocytes in the kainic acid-damaged hippoc ampus have the phenotypic features of type-2 astrocytes”. J. Neurocvtol. 1993; 22: 299–310
   PubMedGoogle Scholar
• Rettig W J, Erickson H. P., Albino A. P., Garin-Chesa P. “Induction of human tenascin (neuronectin) by growth factors and cytokines-cell type specific signals and signalling path ways”. J. Cell. Sci. 1994; 107: 487–497
   PubMed Web of Science ®Google Scholar
• Rifkin D B, Moscatelli D. “Recent developments in the cell biology of basic fibroblast growth factor”. J. Cell. Biol. 1989; 109: 1–6
   PubMed Web of Science ®Google Scholar
• Robbins D S, Shirazi Y., Drysdale B E., Lieberman A., Shin H. S., Shin M. L. “Production of cytotoxic factor for oligodendrocytes by stimulated astrocytes”. J. Immun. 1987; 139: 2593–2597
   PubMed Web of Science ®Google Scholar
• Rutishauser D E, Jessel T. M. “Cell adhesion mol ecules in vertebrate neural development”. Physiol. Rev. 1988; 68: 819–857
   PubMed Web of Science ®Google Scholar
• Saksela O, Rifkin D. B. “Release of basic fibroblast growth factor-heparan sulfate complexes from endothelia) cells by plasminogen activator-mediated proteolytic activity”. J. Cell. Biol. 1990; 110: 767–775
   PubMed Web of Science ®Google Scholar
• Schmidt-Kastner R, Szymas J., Hossman K. A. “Immunochemical study of glial reaction and serum-protein extravasation in relation to neuronal damage in rat hippocampus after ischemia”. Neuroscience. 1990; 38: 527–540
   PubMed Web of Science ®Google Scholar
• Sin A, Carmonella B., Saginati M., Leprini A., Casari G., Baralle F., Zardi L. (a). “Human tenascin: primary struc ture, pre-mRNA splicing patterns and localization of the epitopes recognized by two monoclonal antibodies”. Nucl. Acids. Res. 1991; 19: 525–531
   PubMed Web of Science ®Google Scholar
• Siri A, Knäuper V., Veirana N., Caocci F., Murphy G., Zardi L. “Different susceptibility of small and large human tenascin-C isoforms to degradation by matrix metalloproteases”. J. Biol. Chem. 1995b; 270: 8650–8654
   PubMed Web of Science ®Google Scholar
• Slack J MW, Darlington B. G., Heath Godsave J. K. “Mesoderm induction in early Xenopus embryos by heparinbinding growth factors”. Nature 1987; 326: 197–200
   PubMed Web of Science ®Google Scholar
• Snow D M, Lemmon V., Carrino D. A., Kaplan A. I., Silver J. “Sulfated proteoglycans in astroglial barriers inhibit neurite outgrowth in vitro”. Exp. Neurol. 1990; 109: 111–130
   PubMed Web of Science ®Google Scholar
• Spring J, Beck K., Chiquet-Ehrishmann R. “Two con trary functions of tenascin: dissection of the active sites by recombinant tenascin fragments”. Cell. 1989; 59: 325–334
   PubMed Web of Science ®Google Scholar
• Sriramarao P, Bourdon M A. “A novel tenascin type III repeat is part of a complex of tenascin mRNA splices”. Nucl. Acids. Res. 1993; 21: 163–168
   PubMed Web of Science ®Google Scholar
• Steindler D A, Cooper N. G.E., Faissner A., Schachner M. “Boundaries defined by adhesion molecules during de velopment of the cerebral cortex: the J1/tenascin glycoprotein in the mouse somatosensory cortical barrel field”. Dev. Biol. 1989; 131: 243–260
   PubMed Web of Science ®Google Scholar
• Steindler D A, O'Brien T. F., Laywell E., Harrington K., Faissner A., Schachner M. “Boundaries during normal and abnormal brain development: in vivo and in vitro studies of glia and glycoconjugates”. Exp. Neurol. 1990; 109: 35–36
   PubMed Web of Science ®Google Scholar
• Tucker R P. “The distribution of tenascin and its transcript in the developing avian central nervous system”. J. Exp. Zool. 1991; 259: 78–91
   Google Scholar
• Turnbull J E, Fernig D. G., Ke Y., Wilkinson M. C., Gallager J. T. “Identification of the basic fibroblast growth factor binding sequence in fibroblast heparan sulfate”. J. Biol. Chem. 1992; 267: 10337–10341
   PubMed Web of Science ®Google Scholar
• Van Der Wal E A, Gomez-Pinilla F., Cotman C. W. “Seizure-associated induction of basic fibroblast growth factor and its receptor in the rat brain”. Neuroscience. 1994; 60: 311–323
   PubMed Web of Science ®Google Scholar
• Weller A, Beck S., Ekblom P. “Aminoacid sequence of mouse tenascin and differential expression of two tenascin isoforms during ernbryogenesis”. J. Cell. Biol. 1991; 112: 355–362
   PubMed Web of Science ®Google Scholar
• Woodward W R, Nishi R., Meshul C. K., Williams T. E., Coulombe M., Eckenstein F. P. “Nuclear and cytoplasmic localization of basic fibroblast growth factor in astrocytes and CA2 hippocampal neurons”. The Journal of Neumscience. 1992; 12: 142–152
   PubMed Web of Science ®Google Scholar
• Zhang Y, Anderson P. N., Campbell G., Mohajeri H., Schachner M., Leiberman A. R. “Tenascin-C expression by neurons and glial cells in the rat spinal cord: changes during postnatal development and after dorsal root or sciatic nerve in jury”. J. Neurocytol. 1995; 24: 585–601
   PubMedGoogle Scholar
• Zlotnik I. “The reaction of astrocytes to acute virus infec tions of the central nervous system”. Br. J. Exp. Pathol. 1968; 49: 555–564
   PubMed Web of Science ®Google Scholar