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Original Article

Alterations in neurotrophin and neurotrophin receptor gene expression patterns in the rat central nervous system following perinatal Borna disease virus infection

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Pages 462-477 | Received 21 Dec 1999, Accepted 23 May 2000, Published online: 10 Jul 2009

References

  • Bates B, Rios M, Trumpp A, Chen C, Fan G, Bishop J M, Jaenisch R. Neurotrophin-3 is required for proper cerebellar development. Nat Neurosci 1999; 2: 115–117
  • Bautista J R, Rubin S A, Moran T H, Schwartz G J, Carbone K M. Developmental injury to the cerebellum following perinatal Borna disease virus infection. Brain Res Developmental Brain Res 1995; 90: 45–53
  • Bautista J R, Schwartz G J, de laTorre J C, Moran T H, Carbone K M. Early and persistent abnormalities in rats with neonatally acquired Borna disease virus infection. Brain Res Bull 1994; 34: 31–40
  • Bender K, Balogh P, Bertrand M F, denBieman M, vonDeimling O, Eghtessadi S, Gutman G A, Hedrich H J, Hunt S V, Kluge R, Matsumoto K, Moralejo D H, Nagel M, Portal A, Prokop C M, Seibert R T, van Zutphen L FM. Genetic characterization of inbred strains of the rat (Rattus norvegicus). J Exp Anim Sci 1994; 36: 151–165
  • Breese C R, D'Costa A, Rollins Y D, Adams C, Booze R M, Sonntag W E, Leonard S. Expression of insulinlike growth factor-1 (IGF-1) and IGF-binding protein 2 (IGF-BP2) in the hippocampus following cytotoxic lesion of the dentate gyrus. J Comp Neurol 1996; 369: 388–404
  • Caddy K W, Biscoe T J. Structural and quantitative studies on the normal C3H and Lurcher mutant mouse. Philos Trans R Soc Lond B Biol Sci 1979; 287: 167–201
  • Carbone K M, Park S W, Rubin S A, Waltrip R W, II, Vogelsang G B. Borna disease: association with a maturation defect in the cellular immune response. J Virol 1991; 65: 6154–6164
  • Connor B, Dragunow M. The role of neuronal growth factors in neurodegenerative disorders of the human brain. Brain Res Brain Res Rev 1998; 27: 1–39
  • de la Torre J C. Molecular biology of Borna disease virus: prototype of a new group of animal viruses. J Virol 1994; 68: 7669–7675
  • Dittrich W, Bode L, Ludwig H, Kao M, Schneider K. Learning deficiencies in Borna disease virus-infected but clinically healthy rats. Biol Psychiatry 1989; 26: 818–828
  • Dudov K P, Perry R P. The gene family encoding the mouse ribosomal protein L32 contains a uniquely expressed introncontaining gene and an unmutated processed gene. Cell 1984; 37: 457–468
  • Eisenman L M, Brothers R, Tran M H, Kean R B, Dickson G M, Dietzschold B, Hooper D C. Neonatal Borna disease virus infection in the rat causes a loss of Purkinje cells in the cerebellum. J Neurovirol 1999; 5: 181–189
  • Gao W O, Heintz N, Hatten M E. Cerebellar granule cell neurogenesis is regulated by cell-cell interactions in vitro. Neuron 1991; 6: 705–715
  • Garcia-Estrada J, Garcia-Segura L M, Torres-Aleman I. Expression of insulin-like growth factor I by astrocytes in response to injury. Brain Res 1992; 592: 343–347
  • Gavrieli Y, Sherman Y, Ben-Sasson S A. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J Cell Biol 1992; 119: 493–501
  • Gonzalez-Dunia D, Sauder C, de laTorre J C. Borna disease virus and the brain. Brain Res Bull 1997; 44: 647–664
  • Gosztonyi G, Ludwig H. Borna disease-Neuropathology an.d pathogenesis. Borna disease, H Koprowsk, W I Lipkin. Springer, Berlin 1995; 39–73
  • Gould E, McEwen B S. Neuronal birth and death. Current Opinion in Neurobiology 1993; 3: 676–682
  • Griffin D E, Hardwick J M. Perspective: virus infections and the death of neurons. Trends Microbiol 1999; 7: 155–160
  • Haas B, Becht H, Rott R. Purification and properties of an intranuclear virus-specific antigen from tissue infected with Borna disease virus. J Gen Virol 1986; 67: 235–241
  • Henderson C E. Role of neurotropic factors in neuronal development. Curr Opin Neurobiol 1996; 6: 64–70
  • Herrup K. Role of staggerer gene in determining cell number in cerebellar cortex. I. Granule cell death is an indirect consequence of staggerer gene action. Brain Res 1983; 313: 267–274
  • Herzog S, Rott R. Replication of Borna disease virus in cell cultures. Med Microbiol Immunol 1980; 168: 153–158
  • Hirano N, Kao M, Ludwig H. Persistent, tolerant or subacute infection in Borna disease virus-infected rats. J Gen Virol 1983; 64: 1521–1530
  • Hornig M, Weissenböck H, Horscroft N, Lipkin W I. An infection-based model of neurodevelopmental damage. Proc Natl Acad Sci USA 1999; 96: 12102–12107
  • Ip N Y, Li Y, Yancopoulos G D, Lindsay R M. Cultured hippocampal neurons show responses to BDNF, NT-3, and NT-4, but not NGF. J Neurosci 1993; 13: 3394–3405
  • Kafitz K W, Rose C R, Thoenen H, Konnerth A. Neurotrophin-evoked rapid excitation through TrkB receptors. Nature 1999; 401: 918–921
  • Lewin G R, Barde Y A. Physiology of the neurotrophins. Annual review of Neuroscience 1996; 19: 289–317
  • Lindholm D, Carroll P, Tzimagiogis G, Thoenen H. Autocrine-paracrine regulation of hippocampal neuron survival by IGF-1 and the neurotrophins BDNF, NT-3 and NT-4. Eur J Neurosci 1996; 8: 1452–1460
  • Lindholm D, Hamner S, Zirrgiebel U. Neurotrophins and cerebellar development. Perspect Dev Neurobiol 1997; 5: 83–94
  • Lindsay R M, Wiegand S J, Altar C A, DiStefano P S. Neurotrophic factors: from molecule to man. Trends in Neurosciences 1994; 17: 182–190
  • Lowenstein D H, Arsenault L. The effects of growth factors on the survival and differentiation of cultured dentate gyrus neurons. J. Neurosci 1996; 16: 1759–1769
  • Maisonpierre P C, Belluscio L, Squinto S, Ip N Y, Furth M E, Lindsay R M, Yancopoulos G D. Neurotrophin-3: a neurotrophic factor related to NGF and BDNF. Science 1990; 247: 1446–1451
  • Maisonpierre P C, Le Beau M M, Espinosa R, Ip N Y, Belluscio L, de laMonte S M, Squinto S, Furth M E, Yancopoulos G D. Human and rat brain-derived neurotrophic factor and neurotrophin-3: gene structures, distributions, and chromosomal localizations. Genomics 1991; 10: 558–568
  • McAllister A K, Katz L C, Lo D C. Neurotrophins and synaptic plasticity. Annu Rev Neurosci 1999; 22: 295–318
  • Merlio J P, Ernfors P, Jaber M, Persson H. Molecular cloning of rat trkC and distribution of cells expressing messenger RNAs for members of the trk family in the rat central nervous system. Neuroscience 1992; 51: 513–532
  • Middlemas D S, Lindberg R A, Hunter T. trkB, a neural receptor protein-tyrosine kinase: evidence for a full-length and two truncated receptors. Mol Cell Biol 1991; 11: 143–153
  • Minichiello L, Klein R. TrkB and TrkC neurotrophin receptors cooperate in promoting survival of hippocampal and cerebellar granule neurons. Genes Development 1996; 10: 2849–2858
  • Monjan A A, Cole G A, Nathanson N. Pathogenesis of LCM disease in the rat. Lymphocytic choriomeningitis virus and other arenaviruses, F Lehmann-Grube. Springer, New York 1973; 195–206
  • Monjan A A, Cole G A, Nathanson N. Pathogenesis of cerebellar hypoplasia produced by lymphocytic choriomeningitis virus infection of neonatal rats: protective effect of immunosuppression with antilymphoid serum. Infect Immun 1974; 10: 499–502
  • Mullen R J, Eicher E M, Sidman R L. Purkinje cell degeneration, a new neurological mutation in the mouse. Proc Natl Acad Sci USA 1976; 73: 208–212
  • Murphy L J, Bell G I, Duckworth M L, Friesen H G. Identification, characterization, and regulation of a rat complementary deoxyribonucleic acid which encodes insulin-like growth factor-I. Endocrinology 1987; 121: 684–691
  • Narayan O, Herzog S, Frese K, Scheefers H, Rott R. Behavioral disease in rats caused by immunpathological responses to persistent Borna virus in the brain. Science 1983; 220: 1401–1403
  • Oster-Granite M L, Herndon R M. The development of the cerebellar cortex of the Syrian hamster, Mesocricetus auratus. Foliation, cytoarchitectonic, Golgi, and electron microscopic studies. J Comp Neurol 1976; 169: 443–479
  • Parker M S, O'Callaghan R J, Smith D E, Spence H A. The effect of influenza C virus on the Purkinje cells of chick embryo cerebellum. Int J Dev Neurosci 1994; 12: 461–470
  • Pearce B D, Steffensen S C, Paoletti A D, Henriksen S J, Buchmeier M J. Persistent dentate granule cell hyperexcitability after neonatal infection with lymphocytic choriomeningitis virus. J Neurosci 1996; 16: 220–228
  • Plata-Salaman C R, Ilyin S E, Gayle D, Romanovitch A, Carbone K M. Persistent Borna disease virus infection of neonatal rats causes brain regional changes of mRNAs for cytokines, cytokine receptor components and neuropeptides. Brain Res Bull 1999; 49: 441–451
  • Pletnikov M V, Rubin S A, Schwartz G J, Moran T H, Sobotka T J, Carbone K M. Persistent neonatal Borna disease virus (BDV) infection of the brain causes chronic emotional abnormalities in adult rats. Physiol Behav 1999a; 66: 823–831
  • Pletnikov M Y, Rubin S A, Vasudevan K, Moran T H, Carbone K M. Developmental brain injury associated with abnormal play behavior in neonatally Borna disease virus-infected Lewis rats: a model of autism. Behav Brain Res 1999b; 100: 43–50
  • Raine C S, Fields B N. Reovirus type 3 encephalitis—a virologic and ultrastructural study. J Neuropathol Exp Neurol 1973; 32: 19–33
  • Ramirez J C, Fairen A, Almendral J M. Parvovirus minute virus of mice strain i multiplication and pathogenesis in the newborn mouse brain are restricted to proliferative areas and to migratory cerebellar young neurons. J Virol 1996; 70: 8109–8116
  • Rott R, Becht H. Natural and experimental Borna disease in animals. Borna disease, H Koprowsk, W I Lipkin. Springer, Berlin 1995; 17–30
  • Rubin S A, Bautista J R, Moran T H, Schwartz G J, Carbone K M. Viral teratogenesis: brain developmental damage associated with maturation state at time of infection. Brain Res Dev Brain Res 1999; 112: 237–244
  • Rubin S A, Pletnikov M, Carbone K M. Comparison of the neurovirulence of a vaccine and a wild-type mumps virus strain in the developing rat brain. J Virol 1998a; 72: 8037–8042
  • Rubin S A, Sylves P, Vogel M, Pletnikov M, Moran T H, Schwartz G J, Carbone K M. Borna disease virus-induced hippocampal dentate gyrus damage is associated with spatial learning and memory deficits. Brain Res Bull 1998b; 48: 23–30
  • Sauder C, de laTorre J C. Cytokine expression in the rat central nervous system following perinatal Borna disease virus infection. J Neuroimmunol 1999; 96: 29–45
  • Schneemann A, Schneider P A, Lamb R A, Lipkin W I. The remarkable coding strategy of Borna disease virus: a new member of the nonsegmented negative strand RNA viruses (minireview). Virology 1995; 210: 1–8
  • Schwartz P M, Borghesani P R, Levy R L, Pomeroy S L, Segal R A. Abnormal cerebellar development and foliation in BDNF-/-mice reveals a role for neurotrophins in CNS patterning. Neuron 1997; 19: 269–281
  • Seay A R, Griffin D E. Effects of viral infections on the developing nervous system. Progress in perinatal neurology, R Korobki, C Guilleminaul. Williams and Wilkins, Baltimore 1981; 121–155
  • Simmons D M, Arriza J L, Swanson L W. A complete protocol for in situ hybridization of messenger RNAs in brain and other tissues with radiolabeled single-stranded RNA probes. J Histotechnol 1989; 12: 169–181
  • Smeyne R F, Chu T, Lewin A, Bian F, Crisman S, Kunsch C, Lira S A, Oberdick J. Local control of granule cell generation by cerebellar Purkinje cells. Mol Cell Neurosci 1995; 6: 230–251
  • Snider W D. Functions of the Neurotrophins during nervous system development: What the knockouts are teaching us. Cell 1994; 77: 627–638
  • Tessarollo L. Pleiotropic functions of neurotrophins in development. Cytokine Growth Factor Rev 1998; 9: 125–137
  • Thoenen H. Neurotrophins and neuronal plasticity. Science 1995; 270: 593–597
  • Tsoulfas P, Soppet D, Escandon E, Tessarollo L, Mendoza-Ramirez J L, Rosenthal A, Nikolics K, Parada L F. The rat trkC locus encodes multiple neurogenic receptors that exhibit differential response to neurotrophin-3 in PC12 cells. Neuron 1993; 10: 975–990
  • Valenzuela D M, Maisonpierre P C, Glass D J, Rojas E, Nunez L, Kong Y, Gies D R, Stitt T N, Ip N Y, Yancopoulos G D. Alternative forms of rat TrkC with different functional capabilities. Neuron 1993; 10: 963–974
  • Whittemore S R, Friedman P L, Larhammar D, Persson H, Gonzalez-Carvajal M, Holets V R. Rat beta-nerve growth factor sequence and site of synthesis in the adult hippocampus. J Neurosci Res 1988; 20: 403–410
  • Wood K A, Dipasquale B, Youle R J. In situ labeling of granule cells for apoptosis-associated DNA fragmentation reveals different mechanisms of cell loss in developing cerebellum. Neuron 1993; 11: 621–632
  • Yolken R H, Torrey E F. Viruses, schizophrenia and bipolar disorders. Clin Microbiol Rev 1995; 8: 131–145

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