Rat hippocampus CA1¶
This Use Case places hippocampal neurons into a volume defined by an atlas. The Use Case can be found in Online Use Cases/Circuit Building/Cells placement/Hippocampus CA1.
Approach:¶
The workflow is a sequence of independent steps manipulating volumetric data retrieved from the Neuroinformatics Platform. Each steps defines additional properties of the cells.
The sequence of steps is the following:
Define the region of interest based on the parcellation given by the atlas
Define cell positions based on given neuron densities
Define excitatory/inhibitory properties based on given ratio
Define ME-Type properties based on M-Type and E-Type ratio
Define the morphology to be used based on available morphologies and previously defined properties
Define cell orientation based on a computed orientation field in the volume
Input data:¶
Volume
Volume was adapted from Ropireddy et al., 2012
Cell composition
- Total number of cells: 350000 (adult rat - Bezaire and Soltesz, 2013) 
- EI ratio: 89:11 (adult rat - Bezaire and Soltesz, 2013) 
- Percentage of neuron types from (Bezaire and Soltesz, 2013 - adult rat) 
Morphoelectrical-type composition
We collected 146 electrophysiological single cell recordings from different neuron types (Alex Thomson, Audrey Mercer and colleagues) (Wistar rat - for the methods see Hughes et al., 2000; Pawelzik et al., 2002). We classified the recordings on the basis of stereotypical firing patterns (electrical types, e-types) according to the Petilla Convention (Ascoli et al., 2008) in response to depolarizing step current injections. For some e-types, we had too few recordings and for this reason we restricted the e-types to classical accommodating (cAC), bursting accommodating (bAC) and classical non-accommodating (cNAC). Each morphology type (m-type) can show multiple firing patterns, leading to different morpho-electrical types (me-types).
| cNAC | cAC | bAC | |
|---|---|---|---|
| Ivy | 33.33% | 0.00% | 66.67% | 
| OLM | 0.00% | 100.00% | 0.00% | 
| PVBC | 70.00% | 0.00% | 30.00% | 
| CCKBC | 0.00% | 100.00% | 0.00% | 
| BS | 75.00% | 0.00% | 25.00% | 
| AA | 0.00% | 0.00% | 100.00% | 
| SCA | 0.00% | 100.00% | 0.00% | 
| PPA | 0.00% | 0.00% | 100.00% | 
| IS1 | 0.00% | 100.00% | 0.00% | 
| IS3 | 0.00% | 100.00% | 0.00% | 
| Tri | 0.00% | 100.00% | 0.00% | 
Executing the Use Case¶
Execute the cell (SHIFT + ENTER) in the “Cell Placement Hippocampus Setup” notebook. Then navigate to the “Cell Placement Hippocampus” notebook and execute them sequentially (SHIFT + ENTER).
- positioning neurons - This step computes cell positions with downscaled densities as an illustration. It then displays the cell positions in a widget. 
- defining excitatory/inhibitory property - This step computes the excitatory/inhibitory property based on the provided ratio and displays it in a widget. 
- defining M-Type and E-Type properties - This step computes the M-Type property and E-Type property at the same time and displays them in a widget. - M-Type property: - E-Type property: 
- defining morphology for the cell position - This step computes which morphology will be assigned to a particular cell position. 
- defining cell orientation - This steps computes the 3 vector fields X, Y, and Z and uses them to orient each neuron. - X vector field: - Y vector field: - Z vector field: 








