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AP initiation and propagation in type II cochlear ganglion cell (Hossain et al 2005)
Accession: 54903
The model of type II cochlear ganglion cell was based on the immunostaining of the mouse auditory pathway. Specific antibodies were used to map the distribution of voltage-dependent sodium channels along the two unmyelinated axon-like processes of the bipolar ganglion cells. Three distinct hot spots were detected. A high density of sodium channels was present over the entire trajectory of sensory endings beneath the outer hair cells (the most distal portion of the peripheral axon). THE other two hot spots were localized in the initial segments of both of the axons that flank the unmyelinated bipolar ganglion cell bodies.

A biophysical model indicates that all three hot spots might play important roles in action potential initiation and propagation. For instance, the hot spot in the receptor segment is important for transforming the receptor potentials into a full blown action potential (Supplemental Fig. 1). The hot spots in the two paraganglionic axon initial segments are there to ensure the successful propagation of action potentials from the peripheral to the central axon through the cell body.

The Readme.txt file provides step by step instructions on how to recreate Figures 6 and 7 of Hossain et al., 2005 paper.
Reference: Hossain WA, Antic SD, Yang Y, Rasband MN, Morest DK (2005) Where is the spike generator of the cochlear nerve? Voltage-gated sodium channels in the mouse cochlea. J Neurosci 25:6857-68 [PubMed]

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Model Information (Click on a link to find other models with that property)
Model Type:  
Brain Region(s)/Organism:  
Cell Type(s):   Cochlear Ganglion Cell Type II;
Channel(s):  I Na,t; I K; I M;  
Gap Junctions:  
Receptor(s):  
Gene(s):  
Transmitter(s):  
Simulation Environment:  Neuron;
Model Concept(s):  Action Potential Initiation; Dendritic Action Potentials;
Implementer(s):  Antic, Srdjan [antic at neuron.uchc.edu];
Search NeuronDB for information about:  I Na,t; I K; I M;
Model files   Download zip file   Auto-launch             Help downloading and running models
\
Hossain
Readme.htm
km.mod
kv.mod
na.mod
nach.mod
naf.mod
naxn.mod
mosinit.hoc
Fig7C-hh-dark grey_bar.ses
Fig7C-hh-light grey_bar.ses
Fig7C-NaCh-black_bar.ses
Fig7C-NaCh-dark grey_bar.ses
Fig7C-NaCh-light grey_bar.ses
Fig7C-naf-black_bar.ses
Fig7C-naf-dark grey_bar.ses
Fig7C-naf-light grey_bar.ses
Fig7C-naxn-black.ses
Fig7C-naxn-dark grey_bar.ses
Fig7C-naxn-light grey_bar.ses
Fig7D.ses
Fig7E.ses
Fig6-B.ses
Fig6-C.ses
Fig7B.ses
Fig6-D.ses
Fig6-E.ses
Fig6-F.ses
Fig7A.ses
Fig6-B-inset.ses
                            
Spiral Ganglion Cell Type-2 Model

Spiral Ganglion Cell Type-2 Model (Hossain et al., 2005)

Author: Srdjan Antic, University Connecticut Health Center, 22-DEC-2004

 

Instructions for those who had no previous experience with NEURON!

 

To run the model described in Hossain et al., 2005:

 

  1. Install NEURON from http://www.neuron.yale.edu/neuron/
  2. Make a new folder and copy all “Hossain et al., 2005” files to it.
  3. Run “mknrndll” to compile “mod” files in that new folder.
  4. Once the compiler is finished, go to the folder and double click “mosinit.hoc”.
  5. From the Neuron Main Menu use File --> Load Session.
  6. Pick any session from the list. The names of the sessions correspond with the figure panels in Hossain et al., 2005.
  7. For instance take session “Fig7A”.
  8.  Once the session is loaded you will see the following windows:

a)      Neuron Main Menu

b)     4 Voltage-Axis graphs (Graph[1] to Graph[4])

c)      RunControl

d)     PointProcessManager

e)      Temperature

f)       Global Ra,               and

g)      Cell Builder (CellBuild[0]

  1. In the “RunControl” window click “Init & Run” button.
  2. Graph[3] shows the membrane potential transients obtained in the receptor-neural segment (Receptor[5].v(0.5)) and in the cell body (soma). We are now at “the lower limit of the sensitive range”. Both initial segments (ISP and ISC) are supplied with sodium channels, just enough to pass an action potential from the peripheral to the central axon via the cell body. To check the actual density of hh sodium channels, go to CellBuild[0]  window à Biophysics à Init_Seg_Per.
  3. In the Cell Builder Change gNabar_hh from 929 to 928 in both, Init_Seg_Per (initial segment of the peripheral axon) and Init_Seg_Cen (initial segment of the central axon).
  4. Run the simulation again (in “RunControl” window click “Init & Run” button).
  5. Action potential (AP) now fails to invade the cell body. The only difference between this and previous trial is the removal of 1 pS/um2 from both initial segments.
  6. To create the graph in Figure 7, panel C you need to find the “lower limits of the sensitive range” using four different channel mechanisms. Each bar in the histogram is represented by a session file starting with “Fig7C-“. If you load any of the session files starting with “Fig7C-“ and then decrease the sodium conductance by only 1 pS/um2 from any initial segment, the AP would fail to invade the cell body. Note that the session “Fig7C-hh-black_bar.ses” is missing. This session file is identical to “Fig7A.ses”, and therefore is omitted from the download.

 

>>the end<<

 


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