» Articles » PMID: 27747107

Sniff-Like Patterned Input Results in Long-Term Plasticity at the Rat Olfactory Bulb Mitral and Tufted Cell to Granule Cell Synapse

Overview
Journal Neural Plast
Specialty Neurology
Date 2016 Oct 18
PMID 27747107
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

During odor sensing the activity of principal neurons of the mammalian olfactory bulb, the mitral and tufted cells (MTCs), occurs in repetitive bursts that are synchronized to respiration, reminiscent of hippocampal theta-gamma coupling. Axonless granule cells (GCs) mediate self- and lateral inhibitory interactions between the excitatory MTCs via reciprocal dendrodendritic synapses. We have explored long-term plasticity at this synapse by using a theta burst stimulation (TBS) protocol and variations thereof. GCs were excited via glomerular stimulation in acute brain slices. We find that TBS induces exclusively long-term depression in the majority of experiments, whereas single bursts ("single-sniff paradigm") can elicit both long-term potentiation and depression. Statistical analysis predicts that the mechanism underlying this bidirectional plasticity involves the proportional addition or removal of presynaptic release sites. Gamma stimulation with the same number of APs as in TBS was less efficient in inducing plasticity. Both TBS- and "single-sniff paradigm"-induced plasticity depend on NMDA receptor activation. Since the onset of plasticity is very rapid and requires little extra activity, we propose that these forms of plasticity might play a role already during an ongoing search for odor sources. Our results imply that components of both short-term and long-term olfactory memory may be encoded at this synapse.

Citing Articles

Structural spine plasticity: Learning and forgetting of odor-specific subnetworks in the olfactory bulb.

Meng J, Riecke H PLoS Comput Biol. 2022; 18(10):e1010338.

PMID: 36279303 PMC: 9632792. DOI: 10.1371/journal.pcbi.1010338.


Anatomical and Functional Connectivity at the Dendrodendritic Reciprocal Mitral Cell-Granule Cell Synapse: Impact on Recurrent and Lateral Inhibition.

Aghvami S, Kubota Y, Egger V Front Neural Circuits. 2022; 16:933201.

PMID: 35937203 PMC: 9355734. DOI: 10.3389/fncir.2022.933201.


Olfactory bulb granule cells: specialized to link coactive glomerular columns for percept generation and discrimination of odors.

Egger V, Kuner T Cell Tissue Res. 2021; 383(1):495-506.

PMID: 33404844 PMC: 7873091. DOI: 10.1007/s00441-020-03402-7.


Dendritic integration in olfactory bulb granule cells upon simultaneous multispine activation: Low thresholds for nonlocal spiking activity.

Mueller M, Egger V PLoS Biol. 2020; 18(9):e3000873.

PMID: 32966273 PMC: 7535128. DOI: 10.1371/journal.pbio.3000873.


Vasopressin Cells in the Rodent Olfactory Bulb Resemble Non-Bursting Superficial Tufted Cells and Are Primarily Inhibited upon Olfactory Nerve Stimulation.

Lukas M, Suyama H, Egger V eNeuro. 2019; 6(4).

PMID: 31217196 PMC: 6620393. DOI: 10.1523/ENEURO.0431-18.2019.


References
1.
Phillips M, Sachdev R, Willhite D, Shepherd G . Respiration drives network activity and modulates synaptic and circuit processing of lateral inhibition in the olfactory bulb. J Neurosci. 2012; 32(1):85-98. PMC: 3566643. DOI: 10.1523/JNEUROSCI.4278-11.2012. View

2.
Gao Y, Strowbridge B . Long-term plasticity of excitatory inputs to granule cells in the rat olfactory bulb. Nat Neurosci. 2009; 12(6):731-3. PMC: 2693249. DOI: 10.1038/nn.2319. View

3.
Humeau Y, Luthi A . Dendritic calcium spikes induce bi-directional synaptic plasticity in the lateral amygdala. Neuropharmacology. 2006; 52(1):234-43. DOI: 10.1016/j.neuropharm.2006.07.010. View

4.
Larson J, Munkacsy E . Theta-burst LTP. Brain Res. 2014; 1621:38-50. PMC: 4411212. DOI: 10.1016/j.brainres.2014.10.034. View

5.
Markram H, Gerstner W, Sjostrom P . Spike-timing-dependent plasticity: a comprehensive overview. Front Synaptic Neurosci. 2012; 4:2. PMC: 3395004. DOI: 10.3389/fnsyn.2012.00002. View