 |
|||||
|
|||||
|
|||||
|
|||||
|
|||||
The Journal of Neuroscience, March 5, 2008, 28(10):2332-2341; doi:10.1523/JNEUROSCI.4807-07.2008
Previous Article | Next Article
Cellular/Molecular
Expression of Nonclassical Class I Major Histocompatibility Genes Defines a Tripartite Organization of the Mouse Vomeronasal System
Tomohiro Ishii andPeter Mombaerts The Rockefeller University, New York, New York 10065
Correspondence should be addressed to Peter Mombaerts at his present address: Department of Molecular Neurogenetics, Max Planck Institute of Biophysics, Max-von-Laue-Strasse 3, D-60438 Frankfurt, Germany. Email: peter.mombaerts{at}mpibp-frankfurt.mpg.de
The epithelium of the mouse vomeronasal organ (VNO) consists of apical and basal layers of neuronal cell bodies. Vomeronasal sensory neurons (VSNs) with cell bodies in the basal layer express the G-protein subunit G
o and members of the V2R superfamily of vomeronasal receptor genes and project their axons to the posterior accessory bulb (AOB). V2R+ VSNs also express particular patterns of a family of nine nonclassical class I major histocompatibility Mhc genes, the H2-Mv genes. The function of H2-Mv molecules remains unknown. H2-Mv molecules have been reported to be associated with V2R molecules and have been proposed to participate in pheromone detection. Here, we find that a substantial fraction of V2R+ VSNs does not express these nine H2-Mv genes. The cell bodies of H2-Mv+ and H2-Mv– VSNs reside in the lower and upper sublayers of the basal layer, respectively. This spatial segregation is maintained at the level of the AOB: H2-Mv+ and H2-Mv– VSNs project their axons to the posterior and anterior subdomains of the posterior AOB, respectively. By generating a C-terminal green fluorescent protein fusion protein with M10.2 in gene-targeted mice, we observe subcellular localization of M10.2 not only in dendrites but also in axons of VSNs. Our results reveal a tripartite organization of the VNO and AOB, question the generality of the requirement of these nine H2-Mv molecules for V2R surface expression, and suggest that H2-Mvs can function in both dendrites and axons.
Key words: accessory olfactory bulb; axonal projection; Mhc; sensory neuron; V2R; vomeronasal organ
Received Oct. 23, 2007; revised Dec. 10, 2007; accepted Dec. 28, 2007.
Correspondence should be addressed to Peter Mombaerts at his present address: Department of Molecular Neurogenetics, Max Planck Institute of Biophysics, Max-von-Laue-Strasse 3, D-60438 Frankfurt, Germany. Email: peter.mombaerts{at}mpibp-frankfurt.mpg.de
This article has been cited by other articles:
J. E. A. Prince, J. H. Cho, E. Dumontier, W. Andrews, T. Cutforth, M. Tessier-Lavigne, J. Parnavelas, and J.-F. Cloutier
Robo-2 Controls the Segregation of a Portion of Basal Vomeronasal Sensory Neuron Axons to the Posterior Region of the Accessory Olfactory Bulb
J. Neurosci., November 11, 2009; 29(45): 14211 - 14222.
[Abstract] [Full Text] [PDF]
S. Thams, P. Brodin, S. Plantman, R. Saxelin, K. Karre, and S. Cullheim
Classical Major Histocompatibility Complex Class I Molecules in Motoneurons: New Actors at the Neuromuscular Junction
J. Neurosci., October 28, 2009; 29(43): 13503 - 13515.
[Abstract] [Full Text] [PDF]
R. Tirindelli, M. Dibattista, S. Pifferi, and A. Menini
From Pheromones to Behavior
Physiol Rev, July 1, 2009; 89(3): 921 - 956.
[Abstract] [Full Text] [PDF]
M. J. McConnell, Y. H. Huang, A. Datwani, and C. J. Shatz
H2-Kb and H2-Db regulate cerebellar long-term depression and limit motor learning
PNAS, April 21, 2009; 106(16): 6784 - 6789.
[Abstract] [Full Text] [PDF]
|
|
|
|
 |
|