The main question:

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The main question: How is the topographical information in the olfactory bulb transmitted to and interpreted in the brain to decode the odor map?. Zone-to-Zone Projection (receptor identity). Zone-to-Zone Projection (zone specific markers + olfactory receptor subtypes). coronal slice. - PowerPoint PPT Presentation

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The main question:

How is the topographical information in the olfactory bulb transmitted to and

interpreted in the brain to decode the odor map?

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Zone-to-Zone Projection

(receptor identity)

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Zone-to-Zone Projection

(zone specific markers + olfactory receptor subtypes)

Class I receptor

Class II receptor

(O-MAC)

(OCAM)

coronal slice

Markers:

O-MAC- olfactory specific medium-chain acyl-CoA synthetase (expressed only in the D-zone). OCAM (NCAM2) - olfactory cell adhesion molecule (expressed only in the V-zone).

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ΔIIΔD

Synaptotagmin GFP OCAM

wt

Receptor expression

Two strains of mice

(specific expression of diphtera toxin)

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ΔD mice

ΔD

Synaptotagmin GFP OCAM

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Morphological consequences of ΔD (1)

(Arrangement of glomeruli in the olfactory bulb)

Appropriate glomeruli are missing in ΔD mice (“empty” spaces left – competition?)

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Morphological consequences of ΔD (2)

(otherwise normal cytoarchitecture with distinct layers)

- Appropriate layers were formed (except for missing glomeruli)

TH+ = PGNsGABA+ = GCsSynaptotagmin = synapsesReelin+ = MCs

- Mitral cells in the D domain do not form dendritic terminal tufts (probably no input from OSNs).

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Functional consequences of ΔD (Zif268 + ISI)

Dorsal surface of the OB (ISI):

“unrolled” whole OB (Zif268):

ISI= intrinsic signal imaging

Zif268= immediate early gene

- No ISI odor response in the dorsal surface of the OB.

- Odorants which evoke a response in the V and D domains only activate the V domain in ΔD mice.

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Behavioral consequences of ΔD (1) (odor detection)

- The detection thresholds for pentanal and TMT were not affected, whereas it was ten-times higher for 2MB acid.

- In rats, the most responsive glomerulus for pentanal is located in the V-domain. The same seems to be true in mice, for pentanal and for TMT.

Habituation-dishabituation test:Pentanal - spoiled food (avoidance response) 2MB acid - spoiled food (avoidance response) TMT - fox urine (fear avoidance response)

Thus, ΔD mice can detect odors fairly normally

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Behavioral consequences of ΔD

(2) (odor discrimination)

Thus, ΔD can discriminate between odors normally

- In the odor discrimination test, hungry mice associate 1 odorant with sugar thus and dig longer when smelling it.

- Both wt and ΔD have similar discrimination capabilities.

-Wt mice cannot be trained to associate TMT with sugar (fear avoidance).

- ΔD do not have this problem (but they do detect it).

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Behavioral consequences of ΔD

(3) (Innate avoidance)

Aversive odors

- Innate preference test: in contrast to wt mice, ΔD mice do not display innate avoidance. They are even attracted in some cases.

- Innate avoidance test: in contrast to wt mice, ΔD mice do not display innate avoidance. They are even attracted in some cases. The same is seen in increasing concentrations of 2MB acid.

Thus, the D domain is necessary for innate avoidance

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So… ΔD mice can detect and discriminate between

odors, but they do not exhibit innate avoidance.

Can they be trained?

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Behavioral consequences of ΔD

(3) (Learned avoidance)

- Conditioned avoidance (preference

test): ΔD mice can be conditioned to avoid

aversive odors (LiCl-induced nausea).

Thus, the ΔD mice do not exhibit innate avoidance BUT they do exhibit learned avoidance

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The D domain is necessary for innate avoidance, but is

it sufficient ?

ΔII mice

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ΔII mice

(Do not have any glomeruli except the DI glomeruli)

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(DII but not DI responds to TMT so it is not

avoided)

Behavioral consequences of ΔII

(1) (Innate avoidance)

- Innate avoidance test: in

contrast to ΔD mice, ΔII mice do

display innate avoidance just like

wt mice (except in response to

TMT).

Thus, the D domain is necessary and sufficient for innate avoidance

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Two different “fear pathways”: nature and

nurture

BST

- In wt mice, the BST was strongly activated in the BST-MA, and moderately in the BST-LD.

- This is consistent with the previous observation that TMT activates the BST-MA, leading to the stimulation of the HPA axis (the “stress pathway”) in rats.

- In contrast, the BST-MA was not activated by TMT in the ΔD mice, although the BST-LD was activated as in wild-type mice.

- 2MB acid response was similar between wt and ΔD mice.

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Two different “fear pathways”: nature and

nurture

- TMT strongly activated the HPA axis (measured by ACTH) in wt mice but not in ΔD mice.

- 2MB acid also moderately activated the HPA axis.

“The Stress Pathway”:

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Two different “fear pathways”: nature and nurture

The proposed model:

- TMT activates two different neuronal pathways: one for the innate fear response (in the D-domain) and the other for the learned fear response (in the V-domain).

- For TMT, the D-domain glomeruli activate the olfactory cortex, and subsequently the BST-MA, which activates the HPA axis and causes an increase the plasma ACTH concentration.

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Eliminate a specific population of neurons

Detect morphological consequences

Detect functional consequences

Detect behavioral consequences

Show opposite behavioral consequences

Eliminate all but the specific population of neurons

“Guidelines” for discovering what a neural circuit “does”:

and to be even more persuasive, establish sufficiency (in addition to necessity):

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Question?