| Olfaction is important in the life of most
insects, they use odors to find food, oviposition sites, mates,
and
avoid predators. Insects are excellent model systems for
studying how olfaction works, because their
olfactory system
is numerically simpler –but functionally equivalent- than that
of vertebrates.
But it doesn’t matter if you’re a mouse, a
lizard, or a cockroach, all olfactory systems have to deal with
the same kind of problems! Odorant molecules bear different functional
groups (alcohols, ketones,
aldehydes, ketones) and have varying
carbon chain lengths, and that’s why they smell different to
as.
We also need to know how much of an odorant is in the air
(its concentration, or in other words, how
strong it smells)
and recognize mixtures of odorant mixtures (smells like roses,
a banana, an apple, a mate?).
Odors also vary over time, sometimes
in a very short time scale (milliseconds or less), and the olfactory
system also has to be able to deal with that.

In insects olfaction starts in the antennae.
Upon hitting the antennae, odor molecules interact with olfactory
receptor
cells generating a message which travels down their
axons reaching distinct olfactory neuropil –called glomeruli-
in the first relay station in the olfactory pathway, the antennal
lobe. It is believed that each glomerulus process
information
about a particular odorant or a chemically related group of odorant
molecules.
Glomeruli
are the landmarks of the primary olfactory centers: their positions
and numbers are conserved
across individuals and are characteristic
of each animal species. For instance, in the mice there’re about
1800 glomeruli, and in the sphinx moth there’re 63.
 
In the moth (as in other insects) some
glomeruli are sexually dimorphic. Male moths (but not females)
have
a set of glomeruli exclusively devoted to process information
about the conspecific female sex pheromone.
Similarly, female
moths have a set of glomeruli probably involved in finding and
recognizing suitable oviposition sites.

In the glomeruli, olfactory receptor cells
synapse with neurons that mediate interactions between glomeruli
–
so called local neurons- and with projection neurons.

Projection neurons, which are the output elements of the
antennal lobes, project to higher brain centers
(centers involved
in learning
and memory, and in integration of information of different
sensory modalities).
In the lab I study how odors are represented
in the first relay station in the olfactory pathway, the antennal
lobe.
How I do that?

I stimulate the antenna with host-plant
odorants, and I simultaneously record the electrical activity
of
neurons in the brain. I use fluorescent dyes to stain the
neuron I’ve been recording from and later visualize
its glomerular
affiliation using a laser-scanning confocal microscope.

For instance, using these kind of techniques,
I found that projection neurons with dendritic arborizations
restricted to one of the sexually dimorphic glomeruli n the
female, a lateral large female glomerulus (latLFG),
are preferentially
responsive to one enantiomer (molecules which have identical
physical and chemical
properties and
are just non-superimposable mirror images, like our right and
left hands) of a common
host-plant volatile, linalool. They responded
much better to the (+) than
to the (-) enantiomer of linalool.
It was exciting to find that
projection neurons arborizing in another nearby glomeruli responded
better
to the (-) enantiomer of linalool, and that projection
neurons in other nearby glomeruli might respond
equally well
to both enantiomers of linalool! (Do you want to learn more about
this?)
But what is so important that neurons in the brain care about these enatiomers?
That question –linking neurons
and behavior- was really appealing to
me. One thing I’m doing together with another posdoc in the lab, Jeff
Rifley, and Prof. Wittko Francke, is to look at natural sources of
(+) and (-)linalool. We collect volatiles from
plants and then analyze
their chemical composition using gas chromatography (to separate compounds)
coupled
to mass spectrometry (to identify the compounds).
In other projects, I’m studying how information
about odorants which are behaviorally relevant for both
sexes
(food, for instance) are processed in the antennal lobe, and
how glomeruli interact to process
information about behaviorally
relevant odor blends. Also, when we have time, Heather Stein
and I have
fun with gynandromorphic moths –insects with a transplanted
antennal imagined disk from the opposite sex.
These gynandromorphs
give us an excellent opportunity for studying the role of olfactory
receptor cells in
conferring odor specificity to their postsynaptic
targets.
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