 |
The Journal of Neuroscience, October 20, 2004, 24(42):9341-9352; doi:10.1523/JNEUROSCI.1782-04.2004
Previous Article | Next Article 
Cellular/Molecular
Action Potential Backpropagation and Multiglomerular Signaling in the Rat Vomeronasal System
Jie Ma and
Graeme Lowe
Monell Chemical Senses Center, Philadelphia, Pennsylvania 19104-3308
In the accessory olfactory bulb (AOB), sensory neurons expressing a given vomeronasal receptor (VR) gene send divergent projections to many glomeruli, and second-order neurons (mitral cells) link to multiple glomeruli via branched primary dendrites. We used calcium imaging and paired somadendritic patch-clamp recording to track backpropagated action potentials (APs) in rat AOB primary dendrites. In cells loaded with 150 µM Calcium Orange, somatic spikes elicited fluorescence transients over the entire primary dendritic tree, and the relative fluorescence increment F/F0 increased along all branches from soma to glomeruli. Backpropagation was reliant on Na+ channels: in 1 µM TTX, somatic AP commands evoked dendritic Ca2+ transients that declined steeply with distance. In paired soma- dendritic whole-cell recordings, backpropagated APs were unattenuated up to 200 µm from the soma, whereas subthreshold voltage transients decayed markedly. Computational modeling indicated that the large distal Ca2+ transients are consistent with active, not passive, backpropagation. Genetic tracing in the AOB has suggested homotypic connectivity with individual mitral cell dendritic arbors projecting only to glomeruli targeted by sensory neurons expressing the same VR gene. Non-decremental, non-dichotomous backpropagation in AOB primary dendrites ensures fast, reliable communication between mitral cells and their homotypic glomeruli, binding them into functional modules in accordance with their VR-coded inputs.
Key words: accessory olfactory bulb; mitral cells; calcium; fluorescence; dendrites; modeling
Received May 8, 2004;
revised August 16, 2004;
accepted September 3, 2004.
This article has been cited by other articles:

|
 |

|
 |
 
V. Egger and O. Stroh
Calcium buffering in rodent olfactory bulb granule cells and mitral cells
J. Physiol.,
September 15, 2009;
587(18):
4467 - 4479.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. B. Castro and N. N. Urban
Subthreshold Glutamate Release from Mitral Cell Dendrites
J. Neurosci.,
May 27, 2009;
29(21):
7023 - 7030.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Q. Yuan and T. Knopfel
Olfactory Nerve Stimulation-Induced Calcium Signaling in the Mitral Cell Distal Dendritic Tuft
J Neurophysiol,
April 1, 2006;
95(4):
2417 - 2426.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
N. N. Urban and J. B. Castro
Tuft Calcium Spikes in Accessory Olfactory Bulb Mitral Cells
J. Neurosci.,
May 18, 2005;
25(20):
5024 - 5028.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|