| Neuron | Compartment | Property | Connectivity | Notes |
|---|
| Neocortex V1 interneuron basket PV GABA cell | Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Neocortex V1 interneuron basket PV GABA cell | Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Neocortex M1 interneuron basket PV GABA cell | Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Neocortex M1 interneuron basket PV GABA cell | Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Neocortex U1 interneuron basket PV GABA cell | Soma | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). |
| Neocortex U1 interneuron basket PV GABA cell | Proximal equivalent dendrite | Gaba | from other GABAergic interneurons | GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). Most layer 2/3 pyramidal neurons and interneurons received inhibitory input (presumably GABAergic) from neighboring interneurons in layer 2/3 (Dantzker JL and Callaway EM, 20002 ). Analysis of synaptic input to layer 4 basket cells show that 79% of symmetric synapses could have originated from other layer 4 basket cells. Soma and proximal dendrites received 76% of all the symmetric synapses (Ahmed B et al, 19974 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). |
| Neocortex V1 interneuron basket PV GABA cell | Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
| Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
| Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
| Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
| Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
| Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
| Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
| Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
| Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
| Neocortex M1 interneuron basket PV GABA cell | Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
| Neocortex U1 interneuron basket PV GABA cell | Axon terminal | Gaba | to other GABAergic interneurons | Layer-4 basket cell axons make lateral connection isotropically near cell body ( 50 microm radius), but beyond this core region, anisotropically, preferably within a particular angular sectors cell body (Budd JM and Kisvárday ZF, 20015 ). GABA inactivation of large-basket cells of visual cortex resulted in weakened orientation and direction selectivity, via weakening of long-range lateral inhibition by the basket cells (Kisvárday ZF et al, 20001 ). GABAergic interneurons (basket cells, dendrite-targeting cells, and double-bouquet cells) form reciprocally interconnected intracortical networks in which basket cells play a prominent role, given the strength of innervation and the proximal placement of synapses by basket cells to their postsynaptic targets (Tamás G et al, 19983 ). Layer 4 basket cells in cat visual cortex receive excitatory input from neighboring spiny neurons, resulting in large excitatory EPSPs. One third of spiny cell-smooth cell pair were connected reciprocally (postsynaptic targets include local spiny stellate, pyramidal cells, as well as smooth neurons), but the postsynaptic IPSPs evoked by basket cells are slower, GABAergic, probably of GABAA type (Tarczy-Hornoch K et al, 19986 ). |
