Kainic acid‐induced mossy fiber sprouting and synapse formation in the dentate gyrus of rats

In the kainic acid (KA) model of temporal lobe epilepsy, mossy fibers (MFs) are thought to establish recurrent excitatory synaptic contacts onto granule cells. This hypothesis was tested by intracellular labeling of granule cells with biocytin and identifying their synaptic contacts in the dentate molecular layer with electron microscopic (EM) techniques. Twenty‐three granule cells from KA‐treated animals and 14 granule cells from control rats were examined 2 to 4 months following KA at the light microscopic (LM) level; four cells showing MF sprouting were further characterized at the EM level. Timm staining revealed a time‐dependent growth of aberrant MFs into the dentate inner molecular layer. The degree of sprouting was generally (but not invariably) correlated with the severity and frequency of seizures. LM examination of individual biocytin‐labeled MF axon collaterals revealed enhanced collateralization and significantly increased numbers of synaptic MF boutons in the hilus compared to controls, as well as aberrant MF growth into the granule cell and molecular layers. EM examination of serially reconstructed, biocytin‐labeled MF collaterals in the molecular layer revealed MF boutons that form asymmetrical synapses with dendritic shafts and spines of granule cells, including likely autaptic contacts on parent dendrites of the biocytin‐labeled granule cell. These results constitute ultrastructural evidence for newly formed excitatory recurrent circuits, which might provide a structural basis for enhanced excitation and epileptogenesis in the hippocampus of KA‐treated rats. Hippocampus 10:244–260, 2000 © 2000 Wiley‐Liss, Inc.

[1]  M. Okazaki,et al.  Hippocampal mossy fiber sprouting and synapse formation after status epilepticus in rats: Visualization after retrograde transport of biocytin , 1995, The Journal of comparative neurology.

[2]  J. Cavazos,et al.  Synaptic reorganization in the hippocampus induced by abnormal functional activity. , 1988, Science.

[3]  C. Epstein,et al.  Alumina gel injections into the temporal lobe of rhesus monkeys cause complex partial seizures and morphological changes found in human temporal lobe epilepsy , 1998, The Journal of comparative neurology.

[4]  J. Nadler,et al.  Recurrent mossy fiber pathway in rat dentate gyrus: synaptic currents evoked in presence and absence of seizure-induced growth. , 1999, Journal of neurophysiology.

[5]  T. Babb,et al.  Sprouting of GABAergic and mossy fiber axons in dentate gyrus following intrahippocampal kainate in the rat , 1990, Experimental Neurology.

[6]  C. Ribak,et al.  Five types of basket cell in the hippocampal dentate gyrus: a combined Golgi and electron microscopic study , 1983, Journal of neurocytology.

[7]  C. Stevens,et al.  Excitatory and inhibitory autaptic currents in isolated hippocampal neurons maintained in cell culture. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Lisbeth M. Kraft,et al.  The structure of Ammon's horn , 1968 .

[9]  D. Spencer,et al.  A selective loss of somatostatin in the hippocampus of patients with temporal lobe epilepsy , 1991, Annals of neurology.

[10]  X. Qiao,et al.  Developmental analysis of hippocampal mossy fiber outgrowth in a mutant mouse with inherited spike-wave seizures , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  D. Amaral A golgi study of cell types in the hilar region of the hippocampus in the rat , 1978, The Journal of comparative neurology.

[12]  T. Kosaka,et al.  GABAergic synaptic boutons in the granule cell layer of rat dentate gyrus , 1984, Brain Research.

[13]  W. Cowan,et al.  Electron microscopic studies of the dentate gyrus of the rat. I. Normal structure with special reference to synaptic organization , 1966, The Journal of comparative neurology.

[14]  F. Dudek,et al.  Physiological unmasking of new glutamatergic pathways in the dentate gyrus of hippocampal slices from kainate-induced epileptic rats. , 1998, Journal of neurophysiology.

[15]  K M Harris,et al.  Three‐dimensional analysis of the structure and composition of CA3 branched dendritic spines and their synaptic relationships with mossy fiber boutons in the rat hippocampus , 1992, The Journal of comparative neurology.

[16]  R. Miettinen,et al.  Characterization of Target Cells for Aberrant Mossy Fiber Collaterals in the Dentate Gyrus of Epileptic Rat , 1997, Experimental Neurology.

[17]  E M Glaser,et al.  Autapses in neocortex cerebri: synapses between a pyramidal cell's axon and its own dendrites. , 1972, Brain research.

[18]  A. Obenaus,et al.  Dentate granule cells form novel basal dendrites in a rat model of temporal lobe epilepsy , 1998, Neuroscience.

[19]  P. Schwartzkroin,et al.  Axon arbors and synaptic connections of hippocampal mossy cells in the rat in vivo , 1996, The Journal of comparative neurology.

[20]  Carl W. Cotman,et al.  Selective reinnervation of hippocampal area CA1 and the fascia dentata after destruction of CA3-CA4 afferents with kainic acid , 1980, Brain Research.

[21]  CR Houser,et al.  Altered patterns of dynorphin immunoreactivity suggest mossy fiber reorganization in human hippocampal epilepsy , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[22]  T. Babb,et al.  Single mossy fiber axonal systems of human dentate granule cells studied in hippocampal slices from patients with temporal lobe epilepsy [published erratum appears in J Neurosci 1993 Jun;13(6):following table of contents] , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[23]  P. Schwartzkroin,et al.  Ultrastructural localization of neurotransmitter immunoreactivity in mossy cell axons and their synaptic targets in the rat dentate gyrus , 1997, Hippocampus.

[24]  S. Tanaka,et al.  Heterogeneity of Ictal SPECT Findings in Nine Cases of West Syndrome , 1998, Epilepsia.

[25]  R. S. Sloviter,et al.  The functional organization of the hippocampal dentate gyrus and its relevance to the pathogenesis of temporal lobe epilepsy , 1994, Annals of neurology.

[26]  J H Margerison,et al.  Epilepsy and the temporal lobes. A clinical, electroencephalographic and neuropathological study of the brain in epilepsy, with particular reference to the temporal lobes. , 1966, Brain : a journal of neurology.

[27]  C. Ribak,et al.  Ultrastructure of the pyramidal basket cells in the dentate gyrus of the rat , 1980, The Journal of comparative neurology.

[28]  Y. Ben-Ari,et al.  Brief seizure episodes induce long-term potentiation and mossy fibre sprouting in the hippocampus , 1990, Trends in Neurosciences.

[29]  T. Otis Lasting potentiation of inhibition is associated with an increased number of GABA_A receptors activated during miniature inhibitory postsynaptic currents , 1994 .

[30]  R. Nitsch,et al.  Proportion of parvalbumin‐positive basket cells in the GABAergic innervation of pyramidal and granule cells of the rat hippocampal formation , 1990, The Journal of comparative neurology.

[31]  M. Sperling,et al.  The functional relationship between antidromically evoked field responses of the dentate gyrus and mossy fiber reorganization in temporal lobe epileptic patients , 1992, Brain Research.

[32]  E. Lothman Seizure circuits in the hippocampus and associated structures , 1994, Hippocampus.

[33]  Nadler Jv Kainic acid as a tool for the study of temporal lobe epilepsy , 1981 .

[34]  J. Sørensen,et al.  Correlated Axonal Sprouting and Dendritic Spine Formation during Kainate-Induced Neuronal Morphogenesis in the Dentate Gyrus of Adult Mice , 1997, Experimental Neurology.

[35]  H. Scharfman,et al.  Synaptic connections of dentate granule cells and hilar neurons: Results of paired intracellular recordings and intracellular horseradish peroxidase injections , 1990, Neuroscience.

[36]  C. Zahn Neurologic Care of Pregnant Women with Epilepsy , 1998, Epilepsia.

[37]  Z. Bortolotto,et al.  Seizures produced by pilocarpine in mice: A behavioral, electroencephalographic and morphological analysis , 1984, Brain Research.

[38]  M. Frotscher,et al.  Sprouting in the hippocampus is layer-specific , 1997, Trends in Neurosciences.

[39]  J. E. Franck,et al.  Physiologic and Morphologic Characteristics of Granule Cell Circuitry in Human Epileptic Hippocampus , 1995, Epilepsia.

[40]  T. Babb,et al.  Circuit Mechanisms of Seizures in the Pilocarpine Model of Chronic Epilepsy: Cell Loss and Mossy Fiber Sprouting , 1993, Epilepsia.

[41]  J. Lacaille,et al.  Axonal Sprouting of CA1 Pyramidal Cells in Hyperexcitable Hippocampal Slices of Kainate‐treated Rats , 1996, The European journal of neuroscience.

[42]  D. Spencer,et al.  NMDA receptor activation during epileptiform responses in the dentate gyrus of epileptic patients , 1991, Brain Research.

[43]  T L Babb,et al.  Hippocampal EEG excitability and chronic spontaneous seizures are associated with aberrant synaptic reorganization in the rat intrahippocampal kainate model. , 1993, Electroencephalography and clinical neurophysiology.

[44]  R. Racine,et al.  Modification of seizure activity by electrical stimulation. II. Motor seizure. , 1972, Electroencephalography and clinical neurophysiology.

[45]  F. Dudek,et al.  Electrographic Seizures and New Recurrent Excitatory Circuits in the Dentate Gyrus of Hippocampal Slices from Kainate-Treated Epileptic Rats , 1996, The Journal of Neuroscience.

[46]  T Sutula,et al.  Synaptic and axonal remodeling of mossy fibers in the hilus and supragranular region of the dentate gyrus in kainate‐treated rats , 1998, The Journal of comparative neurology.

[47]  T. Babb,et al.  Synaptic reorganization by mossy fibers in human epileptic fascia dentata , 1991, Neuroscience.

[48]  S. Laurberg,et al.  Lesion‐induced sprouting of hippocampal mossy fiber collaterals to the fascia dentata in developing and adult rats , 1981, The Journal of comparative neurology.

[49]  A. M. Dam,et al.  Epilepsy and Neuron Loss in the Hippocampus , 1980, Epilepsia.

[50]  Thomas P. Sutula,et al.  Progressive neuronal loss induced by kindling: a possible mechanism for mossy fiber synaptic reorganization and hippocampal sclerosis , 1990, Brain Research.

[51]  L Seress,et al.  Morphological variability and developmental aspects of monkey and human granule cells: differences between the rodent and primate dentate gyrus. , 1992, Epilepsy research. Supplement.

[52]  G. Cascino,et al.  Mossy fiber synaptic reorganization in the epileptic human temporal lobe , 1989, Annals of neurology.

[53]  A. Karabelas,et al.  Evidence for autapses in the substantia nigra , 1980, Brain Research.

[54]  F. Dudek,et al.  Electrophysiology of dentate granule cells after kainate-induced synaptic reorganization of the mossy fibers , 1992, Brain Research.

[55]  I. Módy,et al.  Lasting potentiation of inhibition is associated with an increased number of gamma-aminobutyric acid type A receptors activated during miniature inhibitory postsynaptic currents. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[56]  G. Golarai,et al.  Mossy fiber synaptic reorganization induced by kindling: time course of development, progression, and permanence , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[57]  F. Dudek,et al.  Neuron loss, granule cell axon reorganization, and functional changes in the dentate gyrus of epileptic kainate‐treated rats , 1997 .

[58]  C. Ribak,et al.  Direct commissural connections to the basket cells of the hippocampal dentate gyrus: anatomical evidence for feed-forward inhibition , 1984, Journal of neurocytology.

[59]  T. Maehara,et al.  An EEG Study of Patients with Unilateral Diffuse Cortical Dysplasia Who Underwent Hemispherectomy , 1998 .

[60]  P. Somogyi,et al.  Synaptic effects of identified interneurons innervating both interneurons and pyramidal cells in the rat hippocampus , 1997, Neuroscience.

[61]  R. S. Sloviter Possible functional consequences of synaptic reorganization in the dentate gyrus of kainate-treated rats , 1992, Neuroscience Letters.

[62]  Y. Ben-Ari,et al.  Epilepsy induced collateral sprouting of hippocampal mossy fibers: Does it induce the development of ectopic synapses with granule cell dendrites? , 1993, Hippocampus.

[63]  C. Cotman,et al.  Specificity of synaptic growth in brain: remodeling induced by kainic acid lesions. , 1979, Progress in brain research.

[64]  H. Scharfman,et al.  Responses of cells of the rat fascia dentata to prolonged stimulation of the perforant path: Sensitivity of hilar cells and changes in granule cell excitability , 1990, Neuroscience.

[65]  D. Tauck,et al.  Evidence of functional mossy fiber sprouting in hippocampal formation of kainic acid-treated rats , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[66]  F. Dudek,et al.  Chronic seizures and collateral sprouting of dentate mossy fibers after kainic acid treatment in rats , 1988, Brain Research.

[67]  R. S. Sloviter,et al.  Decreased hippocampal inhibition and a selective loss of interneurons in experimental epilepsy. , 1987, Science.

[68]  G. M. Peterson,et al.  Intragranular mossy fibers in rats and gerbils from synapses with the somata and proximal dendrites of basket cells in the dentate gyrus , 1991, Hippocampus.

[69]  D. Spencer,et al.  Epileptiform discharges evoked in hippocampal brain slices from epileptic patients , 1989, Brain Research.

[70]  Y. Ben-Ari,et al.  Limbic seizure and brain damage produced by kainic acid: Mechanisms and relevance to human temporal lobe epilepsy , 1985, Neuroscience.

[71]  G Buzsáki,et al.  GABAergic Cells Are the Major Postsynaptic Targets of Mossy Fibers in the Rat Hippocampus , 1998, The Journal of Neuroscience.

[72]  C. Nitsch,et al.  Parvalbumin disappears from GABAergic CA1 neurons of the gerbil hippocampus with seizure onset while its presence persists in the perforant path , 1997, Brain Research.

[73]  E. Cavalheiro,et al.  The Pilocarpine Model of Epilepsy in Mice , 1996, Epilepsia.

[74]  J. H. Kim,et al.  Hippocampal interneuron loss and plasticity in human temporal lobe epilepsy , 1989, Brain Research.

[75]  R. S. Sloviter,et al.  Permanently altered hippocampal structure, excitability, and inhibition after experimental status epilepticus in the rat: The “dormant basket cell” hypothesis and its possible relevance to temporal lobe epilepsy , 1991, Hippocampus.

[76]  F. Gaarskjaer The organization and development of the hippocampal mossy fiber system , 1986, Brain Research Reviews.

[77]  W. J. Brown,et al.  Temporal Lobe Volumetric Cell Densities in Temporal Lobe Epilepsy , 1984, Epilepsia.

[78]  M. Frotscher,et al.  GABAergic innervation of the rat fascia dentata: A novel type of interneuron in the granule cell layer with extensive axonal arborization in the molecular layer , 1993, The Journal of comparative neurology.

[79]  T L Babb,et al.  Quantified patterns of mossy fiber sprouting and neuron densities in hippocampal and lesional seizures. , 1995, Journal of neurosurgery.

[80]  M. Frotscher,et al.  Divergence of hippocampal mossy fibers , 1994, Synapse.

[81]  House Cr,et al.  Morphological changes in the dentate gyrus in human temporal lobe epilepsy. , 1992 .

[82]  JO McNamara,et al.  Cellular and molecular basis of epilepsy , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[83]  P. Somogyi,et al.  A High Degree of Spatial Selectivity in the Axonal and Dendritic Domains of Physiologically Identified Local‐circuit Neurons in the Dentate Gyms of the Rat Hippocampus , 1993, The European journal of neuroscience.

[84]  B. Longo,et al.  Blockade of pilocarpine- or kainate-induced mossy fiber sprouting by cycloheximide does not prevent subsequent epileptogenesis in rats , 1997, Neuroscience Letters.

[85]  D. Amaral,et al.  The three-dimensional organization of the hippocampal formation: A review of anatomical data , 1989, Neuroscience.

[86]  Ribak Ce Local circuitry of GABAergic basket cells in the dentate gyrus. , 1992 .

[87]  D. Amaral,et al.  A light and electron microscopic analysis of the mossy fibers of the rat dentate gyrus , 1986, The Journal of comparative neurology.

[88]  M. Segal Endogenous bursts underlie seizurelike activity in solitary excitatory hippocampal neurons in microcultures. , 1994, Journal of neurophysiology.

[89]  S. Hsu,et al.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. , 1981, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[90]  W M Cowan,et al.  Quantitative, three‐dimensional analysis of granule cell dendrites in the rat dentate gyrus , 1990, The Journal of comparative neurology.

[91]  I. Módy,et al.  Zinc-Induced Collapse of Augmented Inhibition by GABA in a Temporal Lobe Epilepsy Model , 1996, Science.

[92]  H. Markram,et al.  Frequency and Dendritic Distribution of Autapses Established by Layer 5 Pyramidal Neurons in the Developing Rat Neocortex: Comparison with Synaptic Innervation of Adjacent Neurons of the Same Class , 1996, The Journal of Neuroscience.

[93]  P. Somogyi,et al.  Subdivisions in the Multiple GABAergic Innervation of Granule Cells in the Dentate Gyrus of the Rat Hippocampus , 1993, The European journal of neuroscience.

[94]  Y. Ben-Ari,et al.  From seizures to neo‐synaptogenesis: Intrinsic and extrinsic determinants of mossy fiber sprouting in the adult hippocampus , 1994, Hippocampus.

[95]  B. Stanfield Excessive intra- and supragranular mossy fibers in the dentate gyrus of tottering (tg/tg) mice , 1989, Brain Research.

[96]  Gray Eg Axo-somatic and axo-dendritic synapses of the cerebral cortex: An electron microscope study , 1959 .

[97]  H. Wheal,et al.  Changes in parvalbumin-immunoreactive neurons in the rat hippocampus following a kainic acid lesion , 1993, Neuroscience Letters.

[98]  G. Buzsáki,et al.  Interneurons of the hippocampus , 1998, Hippocampus.

[99]  G Buzsáki,et al.  Interneurons in the Hippocampal Dentate Gyrus: an In Vivo intracellular Study , 1997, The European journal of neuroscience.

[100]  M. Frotscher,et al.  Morphological evidence for the sprouting of inhibitory commissural fibers in response to the lesion of the excitatory entorhinal input to the rat dentate gyrus , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[101]  M. Frotscher,et al.  Lesion‐induced mossy fibers to the molecular layer of the rat fascia dentata: Identification of postsynaptic granule cells by the Golgi‐EM technique , 1983, The Journal of comparative neurology.

[102]  Y. Ben-Ari,et al.  Hippocampal plasticity in the kindling model of epilepsy in rats , 1989, Neuroscience Letters.