Development of neuronal activity and activity-dependent expression of brain-derived neurotrophic factor mRNA in organotypic cultures of rat visual cortex.

We have analyzed in organotypic rat visual cortex cultures the way in which expression of brain-derived neurotrophic factor (BDNF) mRNA depends on synaptically generated spontaneous bioelectric activity (SBA) as monitored by recordings of pyramidal cells. SBA was initially low, but from the fourth week onwards 83% of the neurons fired action potentials at 0.2-1.2 impulses/s in a well-balanced state of excitation and inhibition. BDNF mRNA expression increased during the second week to a level surprisingly similar to the adult visual cortex in vivo, despite the fact that activity rates in vitro were approximately 10-fold lower than rates reported in vivo. Thus, SBA generated by a cortical neuronal network in the absence of sensory input is sufficient to elicit and maintain BDNF expression. The transient BDNF peak occurring after eye opening in vivo did not occur in vitro. A blockade of SBA seems not to alter the expression of neurotrophin (NT)-3 and -4/5, and tyrosine kinase receptor C and B mRNA. However, BDNF expression remained extremely low. A recovery of SBA after a period of blockade concurred with a transient hyperexcitability. BDNF immediately increased, driven by calcium influx through voltage-gated channels in synergy with NMDA receptors. Expression transiently reached high levels in neurons of supragranular layers. Infragranular neurons, although firing action potentials, recovered BDNF expression much slower. After 5 days in vitro recovery, the network had de novo established a balanced state of excitation and inhibition. Distribution and expression level of BDNF mRNA had returned to control. Even in 'adult' cultures an acute blockade of SBA downregulated BDNF, and a subsequent recovery of SBA restored BDNF expression. We conclude that BDNF mRNA expression depends on and responds with a fast kinetic to changes of the SBA. Steady-state levels do not depend on the absolute levels of activity, but more likely on the balance between excitation and inhibition, suggesting a role for BDNF in activity homeostasis.

[1]  E. Castrén,et al.  Interplay between glutamate and gamma-aminobutyric acid transmitter systems in the physiological regulation of brain-derived neurotrophic factor and nerve growth factor synthesis in hippocampal neurons. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[2]  R. Heumann,et al.  BDNF-GFP containing secretory granules are localized in the vicinity of synaptic junctions of cultured cortical neurons. , 1998, Journal of cell science.

[3]  P. C. Murphy,et al.  Cerebral Cortex , 2017, Cerebral Cortex.

[4]  D. McCormick,et al.  Neurotransmitter control of neocortical neuronal activity and excitability. , 1993, Cerebral cortex.

[5]  H. Luhmann,et al.  Development of excitatory and inhibitory postsynaptic potentials in the rat neocortex. , 1995, Perspectives on developmental neurobiology.

[6]  T Nagao,et al.  NMDA receptors mediate neuronal burst firing in rat somatosensory cortex in vivo. , 1993, Neuroreport.

[7]  Carla J. Shatz,et al.  Activity-Dependent Regulation of NMDAR1 Immunoreactivity in the Developing Visual Cortex , 1997, The Journal of Neuroscience.

[8]  L Maffei,et al.  Nerve growth factor and brain‐derived neurotrophic factor increase neurotransmitter release in the rat visual cortex , 1998, The European journal of neuroscience.

[9]  W. Colmers,et al.  Neuropeptide Y suppresses epileptiform activity in rat hippocampus in vitro. , 1997, Journal of neurophysiology.

[10]  P. Wahle,et al.  Patterns of spontaneous activity and morphology of interneuron types in organotypic cortex and thalamus–cortex cultures , 1999, Neuroscience.

[11]  D. Benson,et al.  Activity-Independent Segregation of Excitatory and Inhibitory Synaptic Terminals in Cultured Hippocampal Neurons , 1996, The Journal of Neuroscience.

[12]  K. Maekawa,et al.  Forms of spontaneous and evoked postsynaptic potentials of cortical nerve cells. , 1969, Progress in brain research.

[13]  Tobias Bonhoeffer,et al.  Formation of target-specific neuronal projections in organotypic slice cultures from rat visual cortex , 1990, Nature.

[14]  Steven Finkbeiner,et al.  Ca2+ Influx Regulates BDNF Transcription by a CREB Family Transcription Factor-Dependent Mechanism , 1998, Neuron.

[15]  Michael Miller Maturation of rat visual cortex. I. A quantitative study of Golgi-impregnated pyramidal neurons , 1981, Journal of neurocytology.

[16]  R. McKay,et al.  Cellular targets and trophic functions of neurotrophin-3 in the developing rat hippocampus , 1992, Neuron.

[17]  S. Hestrin,et al.  Frequency-dependent synaptic depression and the balance of excitation and inhibition in the neocortex , 1998, Nature Neuroscience.

[18]  G. Meyer,et al.  Postnatal maturation of nonpyramidal neurons in the visual cortex of the cat , 1984, The Journal of comparative neurology.

[19]  T. Hunter,et al.  trkB, a neural receptor protein-tyrosine kinase: evidence for a full-length and two truncated receptors , 1991, Molecular and cellular biology.

[20]  E. Welker,et al.  Upregulation of BDNF mRNA Expression in the Barrel Cortex of Adult Mice after Sensory Stimulation , 1996, The Journal of Neuroscience.

[21]  M. Segal,et al.  Epileptiform activity in microcultures containing small numbers of hippocampal neurons. , 1990, Journal of neurophysiology.

[22]  C. Gall,et al.  Attenuation of the seizure‐induced expression of BDNF mRNA in adult rat brain by an inhibitor of calcium/calmodulin‐dependent protein kinases , 1998, The European journal of neuroscience.

[23]  G. Carmignoto,et al.  Brain‐derived neurotrophic factor and nerve growth factor potentiate excitatory synaptic transmission in the rat visual cortex. , 1997, The Journal of physiology.

[24]  E. Castrén,et al.  Activity-dependent and hormonal regulation of neurotrophin mRNA levels in the brain--implications for neuronal plasticity. , 1994, Journal of neurobiology.

[25]  M. Bothwell,et al.  Anterograde transport of neurotrophins and axodendritic transfer in the developing visual system , 1996, Nature.

[26]  L Maffei,et al.  Nerve growth factor (NGF) prevents the shift in ocular dominance distribution of visual cortical neurons in monocularly deprived rats , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[27]  A. Friedman,et al.  Intracellular Calcium and Control of Burst Generation in Neurons of Guinea‐Pig Neocortex in Vitro , 1989, The European journal of neuroscience.

[28]  E. Castrén,et al.  The induction of LTP increases BDNF and NGF mRNA but decreases NT-3 mRNA in the dentate gyrus. , 1993, Neuroreport.

[29]  D. McCormick,et al.  Comparative electrophysiology of pyramidal and sparsely spiny stellate neurons of the neocortex. , 1985, Journal of neurophysiology.

[30]  P. Wahle,et al.  NT‐4/5 and LIF, but not NT‐3 and BDNF, promote NPY mRNA expression in cortical neurons in the absence of spontaneous bioelectrical activity , 1998, The European journal of neuroscience.

[31]  Z. Kokaia In Situ Hybridization Histochemistry , 2000, Current protocols in toxicology.

[32]  Rafael Yuste,et al.  Ca2+ accumulations in dendrites of neocortical pyramidal neurons: An apical band and evidence for two functional compartments , 1994, Neuron.

[33]  Howard J. Federoff,et al.  Regulated Release and Polarized Localization of Brain-Derived Neurotrophic Factor in Hippocampal Neurons , 1996, Molecular and Cellular Neuroscience.

[34]  P. Wahle,et al.  Areal Differences of NPY mRNA‐expressing Neurons are Established in the Late Postnatal Rat Visual Cortex In Vivo, but not in Organotypic Cultures , 1995, The European journal of neuroscience.

[35]  Mu-ming Poo,et al.  Fast actions of neurotrophic factors , 1996, Current Opinion in Neurobiology.

[36]  M. Götz,et al.  Differentiation of Transmitter Phenotypes in Rat Cerebral Cortex , 1994, The European journal of neuroscience.

[37]  Niraj S. Desai,et al.  Plasticity in the intrinsic excitability of cortical pyramidal neurons , 1999, Nature Neuroscience.

[38]  G. Yancopoulos,et al.  Alternative forms of rat TrkC with different functional capabilities , 1993, Neuron.

[39]  O. Lindvall,et al.  Rapid increase of BDNF mRNA levels in cortical neurons following spreading depression: regulation by glutamatergic mechanisms independent of seizure activity. , 1993, Brain research. Molecular brain research.

[40]  E. Arenas,et al.  Differential usage of multiple brain-derived neurotrophic factor promoters in the rat brain following neuronal activation. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[41]  K. Hoffmann,et al.  The Corticotectal Projection of the Rat In Vitro: Development, Anatomy and Physiological Characteristics , 1995 .

[42]  D. Debanne,et al.  Organotypic slice cultures: a technique has come of age , 1997, Trends in Neurosciences.

[43]  L. Maffei,et al.  Functional postnatal development of the rat primary visual cortex and the role of visual experience: Dark rearing and monocular deprivation , 1994, Vision Research.

[44]  Lawrence C Katz,et al.  Neurotrophin Regulation of Cortical Dendritic Growth Requires Activity , 1996, Neuron.

[45]  K. Inokuchi,et al.  Increase in activin βA mRNA in rat hippocampus during long‐term potentiation , 1996 .

[46]  O. Lindvall,et al.  Brain Insults in Rats Induce Increased Expression of the BDNF Gene through Differential Use of Multiple Promoters , 1994, The European journal of neuroscience.

[47]  P. Wahle,et al.  Expression of TrkB and TrkC but not BDNF mRNA in neurochemically identified interneurons in rat visual cortex in vivo and in organotypic cultures , 1999, The European journal of neuroscience.

[48]  M. Canossa Neurotrophin release by neurotrophins: Implications fro activity dependent neurons. , 1997 .

[49]  I. Black,et al.  NGF and BDNF are differentially modulated by visual experience in the developing geniculocortical pathway. , 1995, Brain research. Developmental brain research.

[50]  M. Kossut,et al.  Voltage-dependent L-type calcium channels in the development and plasticity of mouse barrel cortex. , 1992, Brain research. Developmental brain research.

[51]  B W Connors,et al.  Synchronized excitation and inhibition driven by intrinsically bursting neurons in neocortex. , 1989, Journal of neurophysiology.

[52]  P. Wahle,et al.  Development and activity-dependent expression of neuronal marker proteins in organotypic cultures of rat visual cortex. , 1996, Brain research. Developmental brain research.

[53]  H. Thoenen,et al.  GABAergic Stimulation Regulates the Phenotype of Hippocampal Interneurons through the Regulation of Brain-Derived Neurotrophic Factor , 1996, Neuron.

[54]  E. Callaway,et al.  The Development of Local, Layer-Specific Visual Cortical Axons in the Absence of Extrinsic Influences and Intrinsic Activity , 1998, The Journal of Neuroscience.

[55]  Sm Hus Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures , 1981 .

[56]  Niraj S. Desai,et al.  Activity-dependent scaling of quantal amplitude in neocortical neurons , 1998, Nature.

[57]  Y. Ben-Ari,et al.  GABA: an excitatory transmitter in early postnatal life , 1991, Trends in Neurosciences.

[58]  J. A. Varela,et al.  Differential Depression at Excitatory and Inhibitory Synapses in Visual Cortex , 1999, The Journal of Neuroscience.

[59]  T. Tsumoto,et al.  Laminar difference in tetanus-induced increase of intracellular Ca2+ in visual cortex of young rats , 1993, Neuroscience Research.

[60]  E. Castrén,et al.  Regulation of brain-derived neurotrophic factor mRNA levels in hippocampus by neuronal activity. , 1998, Progress in brain research.

[61]  Anirvan Ghosh,et al.  Identification of a Signaling Pathway Involved in Calcium Regulation of BDNF Expression , 1998, Neuron.

[62]  A. Larkman,et al.  Correlations between morphology and electrophysiology of pyramidal neurons in slices of rat visual cortex. II. Electrophysiology , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[63]  L. Maffei,et al.  Monocular deprivation decreases brain-derived neurotrophic factor immunoreactivity in the rat visual cortex , 1999, Neuroscience.

[64]  D. O'Leary,et al.  Functional classes of cortical projection neurons develop dendritic distinctions by class-specific sculpting of an early common pattern , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[65]  P. Wahle,et al.  Phenotype Specification of Cortical Neurons During a Period of Molecular Plasticity , 1997, The European journal of neuroscience.

[66]  L. Olson,et al.  Regulation of brain-derived neurotrophic factor (BDNF) expression and release from hippocampal neurons is mediated by non-NMDA type glutamate receptors , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[67]  L. Maffei,et al.  Monocular deprivation decreases the expression of messenger RNA for brain-derived neurotrophic factor in the rat visual cortex , 1995, Neuroscience.

[68]  M. Greenberg,et al.  Distinct roles for bFGF and NT-3 in the regulation of cortical neurogenesis , 1995, Neuron.

[69]  H. Thoenen,et al.  Activity dependent regulation of BDNF and NGF mRNAs in the rat hippocampus is mediated by non‐NMDA glutamate receptors. , 1990, The EMBO journal.

[70]  D. O'Dowd,et al.  Differential Expression of K4-AP Currents and Kv3.1 Potassium Channel Transcripts in Cortical Neurons that Develop Distinct Firing Phenotypes , 1997, The Journal of Neuroscience.

[71]  J. van Pelt,et al.  Growth of pyramidal, but not non‐pyramidal, dendrites in long‐term organotypic explants of neonatal rat neocortex chronically exposed to neurotrophin‐3 , 1998, The European journal of neuroscience.

[72]  B. Connors,et al.  Intrinsic firing patterns of diverse neocortical neurons , 1990, Trends in Neurosciences.

[73]  H. Scharfman Hyperexcitability in combined entorhinal/hippocampal slices of adult rat after exposure to brain-derived neurotrophic factor. , 1997, Journal of neurophysiology.

[74]  H. Thoenen,et al.  Neurotrophin release by neurotrophins: implications for activity-dependent neuronal plasticity. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[75]  D. Plenz,et al.  Neural dynamics in cortex-striatum co-cultures—I. Anatomy and electrophysiology of neuronal cell types , 1996, Neuroscience.

[76]  E. Castrén,et al.  Light regulates expression of brain-derived neurotrophic factor mRNA in rat visual cortex. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[77]  D. Goeddel,et al.  Neurotrophin-5: A novel neurotrophic factor that activates trk and trkB , 1991, Neuron.

[78]  Y. Ho,et al.  Cloning and sequence of a cDNA encoding rat glucose-6-phosphate dehydrogenase. , 1988, Nucleic acids research.

[79]  S. Nelson,et al.  BDNF Has Opposite Effects on the Quantal Amplitude of Pyramidal Neuron and Interneuron Excitatory Synapses , 1998, Neuron.

[80]  M. Waxham,et al.  In situ hybridization histochemistry of Ca2+/calmodulin-dependent protein kinase in developing rat brain , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[81]  C. Gall,et al.  BDNF Protein Measured by a Novel Enzyme Immunoassay in Normal Brain and after Seizure: Partial Disagreement with mRNA Levels , 1995, The European journal of neuroscience.

[82]  D. McCormick,et al.  Control of firing mode of corticotectal and corticopontine layer V burst-generating neurons by norepinephrine, acetylcholine, and 1S,3R- ACPD , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[83]  S M de la Monte,et al.  Human and rat brain-derived neurotrophic factor and neurotrophin-3: gene structures, distributions, and chromosomal localizations. , 1991, Genomics.

[84]  B. Berninger,et al.  Neurotrophins and activity-dependent plasticity of cortical interneurons , 1997, Trends in Neurosciences.

[85]  H. Bradford,et al.  The depolarisation-induced release of [125I]BDNF from brain tissue , 1996, Brain Research.