Olfactory bulb main interneuron periglomerular GABA cell

- - OBmain - - INT - periglomerular - - gaba
Properties are:  Present   Absent 
Input Receptors
Intrinsic Currents
Output Transmitters
Distal equivalent dendrite
Cholinergic Receptors
In triads made up of (i) a cholinergic axon, (ii) one or several periglomerular or granule cell dendrites, and (iii) usually one relay cell dendrite, asymmetric cholinergic synapses were selectively focused on dendrites (gemmules and spines) of periglomerular or granule cells. (Kasa P et al, 19957 ).
Olfactory bulb main mitral GLU cell
 -Distal apical dendrite.Glutamate
Olfactory receptor GLU cell
 -Axon terminal.Glutamate
Olfactory bulb main tufted middle GLU cell
 -Distal apical dendrite.Glutamate
AMPA
Type 1 synapse (Pinching AJ and Powell TP, 197111 ). (Pinching AJ and Powell TP, 197112 ).
Olfactory bulb main mitral GLU cell
 -Distal apical dendrite.Glutamate
Olfactory receptor GLU cell
 -Axon terminal.Glutamate
Olfactory bulb main tufted middle GLU cell
 -Distal apical dendrite.Glutamate
NMDA
Type 1 synapse (Pinching AJ and Powell TP, 197111 ). (Pinching AJ and Powell TP, 197112 ).
GabaA
Synapse of type 2 (Pinching AJ and Powell TP, 197111 ). (Pinching AJ and Powell TP, 197112 ).
GabaB
Synapse of type 2 (Pinching AJ and Powell TP, 197111 ). (Pinching AJ and Powell TP, 197112 ).
I h
(Fried HU et al, 2010 [Mice]16 ). (Holderith NB et al, 2003 [Rat]17 ). histological experiments found Ih expressed in many olfactory bulb cell types including periglomerular cells.
NO
Using double-staining techniques, the distribution of NADPH-diaphorase (ND)- and nitric oxide synthase (NOS)-positive cells was compared in the periglomerular region of typical and atypical rat olfactory glomeruli. The number of ND/NOS-stained periglomerular cells was much higher (P < 0.001) in typical than in atypical glomeruli. (Crespo C et al, 199624 ).
Dopamine
Dopaminergic subdivision of the periglomerular interneurons throughout classes of vertebrates. (Halász N et al, 198225 ).
Gaba
Olfactory bulb main mitral GLU cell
 -Distal apical dendrite.GabaA
Olfactory bulb main tufted middle GLU cell
 -Distal apical dendrite.GabaA
Dendrodendritic synapse onto mitral/tufted cells, of type 2 (Pinching AJ and Powell TP, 197111 ). (Pinching AJ and Powell TP, 197112 ). GAD-positive staining gemmules (i.e., spines) of periglomerular cells also formed reciprocal dendrodentritic synaptic contacts with mitral/tufted cell dentrites. (Ribak CE et al, 197723 ).
Middle equivalent dendrite
I h
(Fried HU et al, 2010 [Mice]16 ). (Holderith NB et al, 2003 [Rat]17 ). histological experiments found Ih expressed in many olfactory bulb cell types including periglomerular cells.
Gaba
Olfactory bulb main mitral GLU cell
 -Middle apical dendrite.GabaA
Proximal equivalent dendrite
mGluR1
(Montague AA and Greer CA, 19991 ).
mGluR2
(Montague AA and Greer CA, 19991 ).
mGluR3
(Montague AA and Greer CA, 19991 ).
Raphe nuclei principal 5HT cell
 -Axon terminal.Serotonin
Serotonin
(Brunert D et al, 201613 ).
I h
(Fried HU et al, 2010 [Mice]16 ). (Holderith NB et al, 2003 [Rat]17 ). histological experiments found Ih expressed in many olfactory bulb cell types including periglomerular cells.
Soma
mGluR1
(Montague AA and Greer CA, 19991 ).
mGluR2
(Montague AA and Greer CA, 19991 ).
mGluR3
(Montague AA and Greer CA, 19991 ).
Possibly from other interneurons in the glomerular layer. Gaba
Spontaneous and electrically driven GABAergic synaptic inputs to PG cells come possibly from other interneurons in the glomerular layer. (Puopolo M and Belluzzi O, 19982 ). Reversed chloride gradients, demonstrated by cytochemical methods, may be responsible for excitatory GABA effects on selected periglomerular neurons (Siklós L et al, 19953 ). Voltage-sensitive dye signals recorded from the glomerular layer reflect activity in periglomerular cells and that Cl- efflux through non-GABAA chloride channels contributes to the postsynaptic depolarization of these cells after olfactory nerve stimulation (Senseman DM, 19964 ). It was shown that stimulation of PG cells results in self-inhibition: release of GABA from an individual PG cell activates GABA(A) receptors on the same neuron (Smith TC and Jahr CE, 20025 ).
primary culture Glycine
Glycine and GABA exert inhibitory actions on olfactory bulb neurons, mitral/tufted cells, granule and periglomerular cells).(Trombley PQ and Shepherd GM, 19946 ).
primary culture Cholinergic Receptors
Periglomerular cells respond to microapplication of GABA, acetylcholine, norepinephrine and glycine with the activation of distinct ionic currents. (Bufler J et al, 19928 ).
culture cells Nicotinic
Application of acetylcholine (ACh) evoked concentration-dependent whole-cell currents (Alkondon M et al, 19969 ).
Primary culture Gaba
In primary culture, GABA and glycine exert inhibitory actions on olfactory bulb neurons, mitral/tufted cells, granule and periglomerular cells (Trombley PQ and Shepherd GM, 19946 ).
Kainate
In an immunocytochemical study in zebrafish 60-70% of cells showed KA receptor mediated labelling (Edwards JG and Michel WC, 200310 ).
NMDA
In an immunocytochemical study in zebrafish all cells resulted in NMDA receptor mediated labelling (Edwards JG and Michel WC, 200310 ).
I Na,t
Depolarisations beyond -40 mV activated a fast transient TTX-sensitive inward current. Once activated, INa declined exponentially to zero following a single exponential. The underlying conductance showed a sigmoidal activation between -40 and +30 mV, with half activation at -17.4 mV and a maximal value of 9.7 nS per neurone. The steady-state inactivation was complete at -30 mV and completely removed at -90 mV, with a midpoint at -56 mV. The activation process could be adequately described by third order kinetics, with time constants ranging from 260 microseconds at -20 mV to 70 microseconds at +50 mV. (Bardoni R et al, 199514 ).
I Calcium
Electrophysiological classification of juxtaglomerular neurons: bursting and standard firing. In contrast to the standard firing neurons, bursting neurons produced a calcium-channel-dependent low-threshold spike (LTS) when depolarized either by current injection or by spontaneous or evoked postsynaptic potentials. Bursting neurons also could oscillate spontaneously. Most bursting cells were either periglomerular cells or external tufted cells. Based on their mode of firing and placement in the bulb circuit, these bursting cells are well situated to drive synchronous oscillations in the olfactory bulb. LVA (low voltage-activated) Ca++ channel may be involved in LTS. (McQuiston AR and Katz LC, 200115 ).
I h
(Fried HU et al, 2010 [Mice]16 ). (Holderith NB et al, 2003 [Rat]17 ). histological experiments found Ih expressed in many olfactory bulb cell types including periglomerular cells.
I A
Two types of PG cells can be distinguished by the presence of delayed-rectifier. R-type has DR current and shows outward rectification under current-clamp; N-type does not. A third type, X-type, has properties of both R- and N-type. Zinc modifies the A-type current, but not the delayed-rectifier type: at given voltages, it reduces A-current peak amplitude, slows its kinetics. Zinc shifts activation and inactivation toward more positive voltage. Thus, at physiological resting potential -55mV, zinc accelerates repolarization. (Puopolo M and Belluzzi O, 199818 ). mRNA of A-channel subunit Kv4.3 is expressed predominantly in periglomerular cells. (In contrast, that of Kv4.2, also of A-channel, is expressed predominantly in granule cells) (Serôdio P and Rudy B, 199819 ).
I h
Ih current: slowly developing hyperpolarisation-activated current with a threshold generally positive to resting potential and with a strongly voltage-dependent activation time constant. The current was Na+- and K+-sensitive, suppressed by external Cs+, and insensitive to Ba++. The Ih should be tonically active at rest, and may contribute to the oscillatory behaviour of the bulbar network (Cadetti L and Belluzzi O, 200120 ).
I p,q
The distribution of the P-type calcium channel in the mammalian central nervous system has been demonstrated immunohistochemically by using a polyclonal specific antibody. Electron microscopic localization revealed labeled patches of plasma membrane on the soma, main dendrites, spiny branchlets, and spines; portions of the smooth endoplasmic reticulum were also labeled. Strong labeling was present in the periglomerular cells of the olfactory bulb, ...etc (Hillman D et al, 199121 ).
I Na,t
PG cells closely resembled previously described periglomerular cells in their morphology. During current clamp recording these neurons were characterized by their lack of action potentials upon depolarization. Consistent with these results no Na+ currents could be elicited in voltage clamp experiments. Two types of outward K+ currents were distinguished: one which inactivated and one which did not. (Bufler J et al, 199222 ).
I K
Re: PG cells: Two types of outward K+ currents were distinguished: one which inactivated and one which did not. (Bufler J et al, 199222 ).
Gaba
GAD-positive staining (Ribak CE et al, 197723 ).
Axon hillock
Axon fiber
Axon terminal
Dopamine
Olfactory bulb main mitral GLU cell
 -Middle apical dendrite.Dopaminergic Receptor
Olfactory bulb main tufted middle GLU cell
 -Middle apical dendrite.Dopaminergic Receptor
Gaba
Olfactory bulb main mitral GLU cell
 -Middle apical dendrite.GabaA
Olfactory bulb main tufted middle GLU cell
 -Middle apical dendrite.GabaA
NO
Classical References: first publications on each compartmental property; search PubMed for complete list
1.  Montague AA and Greer CA. (1999) Differential distribution of ionotropic glutamate receptor subunits in the rat olfactory bulb. J Comp Neurol 405:233-46.
2.  Puopolo M and Belluzzi O. (1998) Inhibitory synapses among interneurons in the glomerular layer of rat and frog olfactory bulbs. J Neurophysiol 80:344-9 [Journal] .
3.  Siklós L, Rickmann M, Joó F, Freeman WJ and Wolff JR. (1995) Chloride is preferentially accumulated in a subpopulation of dendrites and periglomerular cells of the main olfactory bulb in adult rats. Neuroscience 64:165-72.
4.  Senseman DM. (1996) High-speed optical imaging of afferent flow through rat olfactory bulb slices: voltage-sensitive dye signals reveal periglomerular cell activity. J Neurosci 16:313-24.
5.  Smith TC and Jahr CE. (2002) Self-inhibition of olfactory bulb neurons. Nat Neurosci 5:760-6 [Journal] .
6.  Trombley PQ and Shepherd GM. (1994) Glycine exerts potent inhibitory actions on mammalian olfactory bulb neurons. J Neurophysiol 71:761-7 [Journal] .
7.  Kasa P, Hlavati I, Dobo E, Wolff A, Joo F and Wolff JR. (1995) Synaptic and non-synaptic cholinergic innervation of the various types of neurons in the main olfactory bulb of adult rat: immunocytochemistry of choline acetyltransferase. Neuroscience 67:667-77.
8.  Bufler J, Zufall F, Franke C and Hatt H. (1992) Patch-clamp recordings of spiking and nonspiking interneurons from rabbit olfactory bulb slices: GABA- and other transmitter receptors. J Comp Physiol A 170:153-9.
9.  Alkondon M, Rocha ES, Maelicke A and Albuquerque EX. (1996) Diversity of nicotinic acetylcholine receptors in rat brain. V. alpha-Bungarotoxin-sensitive nicotinic receptors in olfactory bulb neurons and presynaptic modulation of glutamate release. J Pharmacol Exp Ther 278:1460-71.
10.  Edwards JG and Michel WC. (2003) Pharmacological characterization of ionotropic glutamate receptors in the zebrafish olfactory bulb. Neuroscience 122:1037-47.
11.  Pinching AJ and Powell TP. (1971) The neuropil of the glomeruli of the olfactory bulb. J Cell Sci 9:347-77.
12.  Pinching AJ and Powell TP. (1971) The neuron types of the glomerular layer of the olfactory bulb. J Cell Sci 9:305-45.
13.  Brunert D, Tsuno Y, Rothermel M, Shipley MT and Wachowiak M. (2016) Cell-Type-Specific Modulation of Sensory Responses in Olfactory Bulb Circuits by Serotonergic Projections from the Raphe Nuclei. J Neurosci 36:6820-35 [Journal] .
14.  Bardoni R, Magherini PC and Belluzzi O. (1995) Sodium current in periglomerular cells of frog olfactory bulb in vitro. Brain Res 703:19-25.
15.  McQuiston AR and Katz LC. (2001) Electrophysiology of interneurons in the glomerular layer of the rat olfactory bulb. J Neurophysiol 86:1899-907 [Journal] .
16.  Fried HU, Kaupp UB and Müller F. (2010) Hyperpolarization-activated and cyclic nucleotide-gated channels are differentially expressed in juxtaglomerular cells in the olfactory bulb of mice. Cell Tissue Res 339:463-79 [Journal] .
17.  Holderith NB, Shigemoto R and Nusser Z. (2003) Cell type-dependent expression of HCN1 in the main olfactory bulb. Eur J Neurosci 18:344-54.
18.  Puopolo M and Belluzzi O. (1998) Functional heterogeneity of periglomerular cells in the rat olfactory bulb. Eur J Neurosci 10:1073-83.
19.  Serôdio P and Rudy B. (1998) Differential expression of Kv4 K+ channel subunits mediating subthreshold transient K+ (A-type) currents in rat brain. J Neurophysiol 79:1081-91 [Journal] .
20.  Cadetti L and Belluzzi O. (2001) Hyperpolarisation-activated current in glomerular cells of the rat olfactory bulb. Neuroreport 12:3117-20 [Journal] .
21.  Hillman D, Chen S, Aung TT, Cherksey B, Sugimori M and Llinás RR. (1991) Localization of P-type calcium channels in the central nervous system. Proc Natl Acad Sci U S A 88:7076-80.
22.  Bufler J, Zufall F, Franke C and Hatt H. (1992) Patch-clamp recordings of spiking and nonspiking interneurons from rabbit olfactory bulb slices: membrane properties and ionic currents. J Comp Physiol A 170:145-52.
23.  Ribak CE, Vaughn JE, Saito K, Barber R and Roberts E. (1977) Glutamate decarboxylase localization in neurons of the olfactory bulb. Brain Res 126:1-18.
24.  Crespo C, Porteros A, Arévalo R, Briñón JG, Aijón J and Alonso JR. (1996) Segregated distribution of nitric oxide synthase-positive cells in the periglomerular region of typical and atypical olfactory glomeruli. Neurosci Lett 205:149-52.
25.  Halász N, Nowycky M, Hökfelt T, Shepherd GM, Markey K and Goldstein M. (1982) Dopaminergic periglomerular cells in the turtle olfactory bulb. Brain Res Bull 9:383-9.