Innervation of burst firing spiny interneurons by pyramidal cells in deep layers of rat somatomotor cortex: Paired intracellular recordings with biocytin filling

Intracellular recordings were obtained from a class of neuron defined electrophysiologically as burst firing interneurons in layers V and VI in slices of adult rat somatomotor cortex. Four of these cells were recovered histologically. These four cells had resting membrane potentials between -68 and -80 mV, a mean input resistance of 77 +/- 16.2 M omega (measured from the voltage deflection produced by a 100 ms, 0.5 nA hyperpolarizing pulse delivered from a membrane potential of -80 mV) and responded to injections of depolarizing current from membrane potentials negative of -70 to -75 mV with an initial burst of action potentials followed by a complex afterhyperpolarization. In response to injection of larger (0.5-1.5 nA) hyperpolarizing current pulses from membrane potentials between -60 and -70 mV, 15 of 20 burst firing cells (three of four recovered histologically) that were tested displayed delayed inward rectification, and in all 20 cells of this type, responses to large negative current pulses were followed by a rebound depolarization that could initiate action potentials. Filling of four of these cells with biocytin and subsequent histological processing revealed that they were bitufted with sparsely to medium spiny dendrites and extensive local axon ramifications. These neurons are similar to low threshold spiking cells [Kawaguchi (1993) J. Neurophysiol. 69, 416-431]. Ultrastructural examination of the axons of three cells revealed that of 53 labelled terminals studied, the majority formed synaptic contacts with dendritic shafts. Filling neurons with biocytin during paired intracellular recordings resulted in three well labelled interneurons, each of which was postsynaptic to a simultaneously recorded pyramidal neuron. In these pairs both cells were identified, but the presynaptic axon was poorly labelled in one. In one of the two pairs in which the pre- and postsynaptic neurons were fully recovered, light microscopic assessment indicated that the axon of the presynaptic pyramid formed 12 close appositions with dendrites of the postsynaptic interneuron. Six of these appositions were examined at the electron microscopic level and were identified as possible synaptic contacts. In the other pair three of six close appositions observed at the light level were verified as possible synaptic connections at the ultrastructural level. These correlated electrophysiological and anatomical studies provide the first evidence for connections from pyramid to burst firing interneurons in the neocortex and indicate that these connections can be mediated by multiple synaptic contacts. The accompanying paper describes the functional properties of these connections.

[1]  E. White,et al.  Intrinsic circuitry: Synapses involving the local axon collaterals of corticocortical projection neurons in the mouse primary somatosensory cortex , 1990, The Journal of comparative neurology.

[2]  E. G. Jones,et al.  Synapses of double bouquet cells in monkey cerebral cortex visualized by calbindin immunoreactivity , 1989, Brain Research.

[3]  C. Blakemore,et al.  Pyramidal neurons in layer 5 of the rat visual cortex. I. Correlation among cell morphology, intrinsic electrophysiological properties, and axon targets , 1994, The Journal of comparative neurology.

[4]  E. White,et al.  Intrinsic circuitry involving the local axon collaterals of corticothalamic projection cells in mouse SmI cortex , 1987, The Journal of comparative neurology.

[5]  P. Branchereau,et al.  Analysis of synaptic inputs and targets of physiologically characterized neurons in rat frontal cortex: Combined in vivo intracellular recording and immunolabeling , 1994, Synapse.

[6]  Peter Somogyi,et al.  Diverse sources of hippocampal unitary inhibitory postsynaptic potentials and the number of synaptic release sites , 1994, Nature.

[7]  Françoise Condé,et al.  Local circuit neurons immunoreactive for calretinin, calbindin D‐28k or parvalbumin in monkey prefronatal cortex: Distribution and morphology , 1994, The Journal of comparative neurology.

[8]  T. Wiesel,et al.  Targets of horizontal connections in macaque primary visual cortex , 1991, The Journal of comparative neurology.

[9]  B. Sakmann,et al.  Differences in Ca2+ permeability of AMPA-type glutamate receptor channels in neocortical neurons caused by differential GluR-B subunit expression , 1994, Neuron.

[10]  C. Sotelo,et al.  Ultrastructural features of the isolated suprasylvian gyrus in the cat , 1974, The Journal of comparative neurology.

[11]  J. E. Franck,et al.  Local circuit synaptic interactions between CA1 pyramidal cells and interneurons in the kainate‐lesioned hyperexcitable hippocampus , 1991, Hippocampus.

[12]  J. Deuchars,et al.  Single axon excitatory postsynaptic potentials in neocortical interneurons exhibit pronounced paired pulse facilitation , 1993, Neuroscience.

[13]  J. Deuchars,et al.  Single axon fast inhibitory postsynaptic potentials elicited by a sparsely spiny interneuron in rat neocortex , 1995, Neuroscience.

[14]  N. Tamamaki,et al.  Hippocampal pyramidal cells excite inhibitory neurons through a single release site , 1993, Nature.

[15]  J. Lacaille,et al.  Local circuit interactions between oriens/alveus interneurons and CA1 pyramidal cells in hippocampal slices: electrophysiology and morphology , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  J. Deuchars,et al.  Temporal and spatial properties of local circuits in neocortex , 1994, Trends in Neurosciences.

[17]  D. Prince,et al.  Burst generating and regular spiking layer 5 pyramidal neurons of rat neocortex have different morphological features , 1990, The Journal of comparative neurology.

[18]  Y. Kawaguchi Physiological subgroups of nonpyramidal cells with specific morphological characteristics in layer II/III of rat frontal cortex , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[19]  V. Braitenberg,et al.  Classification of Cortical Neurons , 1991 .

[20]  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.

[21]  D. Whitteridge,et al.  Connections between pyramidal neurons in layer 5 of cat visual cortex (area 17) , 1987, The Journal of comparative neurology.

[22]  T. Freund,et al.  GABAergic interneurons containing calbindin D28K or somatostatin are major targets of GABAergic basal forebrain afferents in the rat neocortex , 1991, The Journal of comparative neurology.

[23]  Shaul Hestrin,et al.  Different glutamate receptor channels mediate fast excitatory synaptic currents in inhibitory and excitatory cortical neurons , 1993, Neuron.

[24]  A. Thomson,et al.  Voltage-dependent currents prolong single-axon postsynaptic potentials in layer III pyramidal neurons in rat neocortical slices. , 1988, Journal of neurophysiology.

[25]  J. DeFelipe,et al.  The pyramidal neuron of the cerebral cortex: Morphological and chemical characteristics of the synaptic inputs , 1992, Progress in Neurobiology.

[26]  Y. Kubota,et al.  Correlation of physiological subgroupings of nonpyramidal cells with parvalbumin- and calbindinD28k-immunoreactive neurons in layer V of rat frontal cortex. , 1993, Journal of neurophysiology.

[27]  L. Nowak,et al.  Quisqualate‐ and kainate‐activated channels in mouse central neurones in culture. , 1988, The Journal of physiology.

[28]  S. Levay,et al.  Synaptic patterns in the visual cortex of the cat and monkey. Electron microscopy of Golgi Preparations , 1973, The Journal of comparative neurology.

[29]  M. Celio,et al.  Calbindin D-28k and parvalbumin in the rat nervous system , 1990, Neuroscience.

[30]  E. Costa,et al.  Glutamate-activated currents in outside-out patches from spiny versus aspiny hilar neurons of rat hippocampal slices , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[31]  J. Hornung,et al.  The Selective innervation by serotoninergic axons of calbindin‐containing interneurons in the neocortex and hippocampus of the marmoset , 1992, The Journal of comparative neurology.

[32]  J. Deuchars,et al.  Large, deep layer pyramid-pyramid single axon EPSPs in slices of rat motor cortex display paired pulse and frequency-dependent depression, mediated presynaptically and self-facilitation, mediated postsynaptically. , 1993, Journal of neurophysiology.

[33]  E. White,et al.  A quantitative study of thalamocortical and other synapses involving the apical dendrites of corticothalamic projection cells in mouse SmI cortex , 1982, Journal of neurocytology.

[34]  J Deuchars,et al.  Relationships between morphology and physiology of pyramid‐pyramid single axon connections in rat neocortex in vitro. , 1994, The Journal of physiology.

[35]  P. Somogyi,et al.  The study of golgi stained cells and of experimental degeneration under the electron microscope: A direct method for the identification in the visual cortex of three successive links in a neuron chain , 1978, Neuroscience.

[36]  E. G. Jones,et al.  A microcolumnar structure of monkey cerebral cortex revealed by immunocytochemical studies of double bouquet cell axons , 1990, Neuroscience.

[37]  J. DeFelipe,et al.  Neocortical neuronal diversity: chemical heterogeneity revealed by colocalization studies of classic neurotransmitters, neuropeptides, calcium-binding proteins, and cell surface molecules. , 1993, Cerebral cortex.

[38]  J. Deuchars,et al.  Properties of single axon excitatory postsynaptic potentials elicited in spiny interneurons by action potentials in pyramidal neurons in slices of rat neocortex , 1995, Neuroscience.

[39]  J SZENTAGOTHAI,et al.  THE USE OF DEGENERATION METHODS IN THE INVESTIGATION OF SHORT NEURONAL CONNEXIONS. , 1965, Progress in brain research.

[40]  A. Thomson,et al.  Fluctuations in pyramid-pyramid excitatory postsynaptic potentials modified by presynaptic firing pattern and postsynaptic membrane potential using paired intracellular recordings in rat neocortex , 1993, Neuroscience.

[41]  U. Eysel,et al.  Cellular organization of reciprocal patchy networks in layer III of cat visual cortex (area 17) , 1992, Neuroscience.

[42]  H Korn,et al.  Excitatory synaptic connections onto rat hippocampal inhibitory cells may involve a single transmitter release site. , 1994, The Journal of physiology.

[43]  K. Stratford,et al.  Synaptic transmission between individual pyramidal neurons of the rat visual cortex in vitro , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.