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Givaudan-Roure Lecture - Association for Chemoreception Sciences

Givaudan-Roure Lecture - Association for Chemoreception Sciences

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37 Poster [ ] Vomeronasal Organ<br />

EXPRESSION PATTERN OF GENES FOR NOTCH<br />

SIGNALING PATHWAY IN MOUSE VOMERONASAL ORGAN<br />

DURING ONTOGENY AND REGENERATION AFTER<br />

REMOVAL OF ACCESSORY OLFACTORY BULB.<br />

Wakabayashi Y. 1, Ichikawa M. 2 1Research Fellow of the Japan Society<br />

<strong>for</strong> the Promotion of Science, Tokyo, Japan; 2Dep Basic Tech and<br />

Facilities, Tokyo Metropol Inst Neurosci, Tokyo, Japan<br />

Vomeronasal receptor neurons (VRNs) proliferate and differentiate<br />

continuously throughout life. Proliferation of VRNs mainly occurs in<br />

the marginal region of the sensory epithelium of adult vomeronasal<br />

organ (VNO). The Notch signaling pathway is involved in cell fate<br />

decisions and differentiation during developmental CNS. We have<br />

studied whether Notch signaling pathway involves in differentiation<br />

and proliferation of VRNs during ontogeny and regeneration.<br />

In this study, we examined the expression patterns of Notch and<br />

their ligands, Delta and Jagged, using in situ hybridization during<br />

ontogeny and regeneration after removal of accessory olfactory bulb<br />

(AOBX) in mice. In adult VNO, a few Notch1(+), Delta1(+) and<br />

BrdU(+) cells appeared only in the marginal region, whereas Jagged2<br />

was expressed in all VRNs. Notch1(+), Delta1(+) and BrdU(+) cells<br />

located close to the basal lamia at embryonic days 14.5 and 16.5,<br />

whereas expression level of Jagged2 was very low in comparison with<br />

adult. At AOBX day2, number and location of Notch1(+), Delta1(+)<br />

and BrdU(+) cells did not change. Expression pattern of Jagged2 did<br />

not change. At AOBX day7, large amount of Notch1(+), Delta1(+) and<br />

BrdU(+) cells appeared in the marginal region, whereas expression<br />

pattern of Jagged2 did not change. These results suggested that the<br />

interaction of Notch1(+) and Delta1(+) cells play important roles in<br />

vomeronasal neurogenesis of VNO during ontogeny as well as<br />

regeneration after AOBX mice.<br />

38 Poster [ ] Vomeronasal Organ<br />

THE ROLE OF THE VOMERONASAL SYSTEM IN FOOD<br />

PREFERENCES OF THE GRAY SHORT-TAILED OPOSSUM,<br />

MONODELPHIS DOMESTICA<br />

Daniels Y. 1, Halpern M. 2, Zuri I. 1 1Anatomy and Cell Biology,<br />

Downstate Medical Center, Brooklyn, NY; 2Anatomy & Cell Biology,<br />

Downstate Medical Center, Brooklyn, NY<br />

The vomeronasal system (VNS) is usually considered primarily a<br />

pheromone-detecting system. In snakes and lizards, this system is also<br />

important <strong>for</strong> feeding behavior. To date, no studies have reported<br />

feeding deficits in mammals deprived of a functional VNS. M.<br />

domestica is considered a primitive mammalian species that was<br />

recently introduced into laboratories. Since these opossums respond to a<br />

variety of foods, they are a good model to investigate the role of the<br />

VNS in food preferences in mammals.<br />

The six male and seven female gray short-tailed opossums used in<br />

this study were simultaneously presented with four foods, one from<br />

each of the following food groups: fruits (apples, oranges, peaches,<br />

cantaloupes), meats (mealworms, chicken, pork, crickets), processed<br />

vegetables (raisin bran, cheerios, whole wheat bread, bagel) and<br />

unprocessed vegetables (corn, peppers, carrots, broccoli). Be<strong>for</strong>e<br />

blocking access to the vomeronasal organ (VNO) with gel foam and<br />

Crazy Glue, the opossums selected meats most frequently and fruits<br />

more frequently than processed and unprocessed vegetables. Following<br />

VNO blockage, the opossums demonstrated no preference between the<br />

different food groups. This study suggests that without a functional<br />

vomeronasal organ, the food preferences of gray short-tailed opossums<br />

are significantly impaired.<br />

Supported by NIDCD Grant # DC02745.<br />

10<br />

39 Slide [ ] Vomeronasal Organ<br />

CHEMO-INVESTIGATORY BEHAVIOUR OF MALE MICE IN<br />

DETECTING ESTRUS: ROLE OF OLFACTORY-<br />

VOMERONASAL SYSTEM<br />

Raman S.A. 1 1Animal Scinece, Bharathidasan University,<br />

Trichirappalli, India<br />

S.ACHIRAMAN AND G.ARCHUNAN<br />

Department of Animal Science, Bharathidasan University<br />

Tiruchirappalli-620 024, Tamilnadu.<br />

INDIA<br />

achiraman_s@yahoo.co.in<br />

The aim of the present study is to evaluate whether the male<br />

mouse is capable of discriminating the female urinary odour of different<br />

reproductive phases (with a view to detect estrus using Y-maze<br />

apparatus and to establish the relationship of olfactory - vomeronasal<br />

system and chemo-investigatory behaviour in estrus detection. Hence,<br />

normal, vomeronasal organ (VNO)-ablated and Zinc Sulphate-irrigated<br />

mouse were used as test animals. Various behaviours such as frequency<br />

of visit, duration of visit, sniffing, licking, body rubbing and grooming<br />

were recorded. The normal mice frequently visited and devoted more<br />

time in delivering various behaviours towards the estrus urine sample in<br />

comparison to that of non-estrus urine. The VNO-ablated mice showed<br />

significant reduction in response to estrus urine (duration of visit and<br />

self-grooming) than that of ZnSO4-irrigated mice. However, the<br />

ZnSO4-irrigated mice showed significant reduction in frequency of<br />

visits to the urine samples. These results clearly reveal that the VNO<br />

play a significant role in the detection of estrus in mice. The present<br />

results also suggest that male mice preferentially communicate sexual<br />

interest via self-grooming towards the opposite sex. By self-grooming<br />

at higher rates, male mice may be broadcasting scents to attract<br />

potential mates or to in<strong>for</strong>m their willingness to mate.<br />

40 Poster [ ] Vomeronasal Organ<br />

NEUROGENESIS, MIGRATION AND APOPTOSIS IN THE<br />

VOMERONASAL EPITHELIUM OF ADULT MICE<br />

Martinez-Marcos A. 1, Quan W. 2, Jia C. 2, Halpern M. 3 1Departamento<br />

de Ciencias Medicas, Universidad de Castilla-La Mancha, Albacete,<br />

Albacete, Spain; 2Anatomy and Cell Biology, Downstate Medical<br />

Center, Brooklyn, NY; 3Anatomy & Cell Biology, Downstate Medical<br />

Center, Brooklyn, NY<br />

Neurogenesis in the adult mouse vomeronasal organ appears to occur<br />

in the central regions, but is more prevalent at the edges of sensory<br />

epithelium. Basal cells at the center of the epithelium participate in cell<br />

replacement. It is unknown whether dividing cells at the edges<br />

constitute a reservoir <strong>for</strong> growth, become apoptotic or participate in<br />

neural turnover. This latter possibility implies a process of horizontal<br />

migration. The present work addresses this controversy by injecting<br />

bromodeoxyuridine in adult mice and allowing them to survive <strong>for</strong><br />

various intervals. The vertical and horizontal position of labeled cells<br />

was analyzed as a function of time. Both, vertical and horizontal<br />

migration of labeled cells were detected. Cells at the center of the<br />

epithelium migrate vertically to become neurons as demonstrated by coexpression<br />

of olfactory marker protein. Cells at the edges migrate<br />

horizontally toward the center. After 42 days, however, they have<br />

migrated less than 10% of the distance from the edge (0%) to the center<br />

of the epithelium (100%), thus making it likely that if these cells<br />

participate in neural turnover it is only in marginal regions. The pattern<br />

of distribution of apoptotic cells has been studied and, interestingly, it is<br />

similar to that of dividing cells. These results support the idea that<br />

sensory cell renewal in the mouse vomeronasal organ occurs through a<br />

process of vertical migration. Supported by grant DC02745.

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