With the current launch of the Allen Cell Types Database, we include electrophysiological recordings from over 700 individual cells, a sub-set of which also include [morphological] reconstruction and [#Neuronal Models]. There are several methods to search this database; 1) enable specific [filter parameters] by selecting from the "Filters" menu, 2) Select a cell from the "[#Cell Location]" map, 3) use the slider bars in the [Parallel Coordinate Plot] or 4) selecting from one of the curated [Electrophysiological or Morphological] searches.
To filter the neurons in your list of results, select from the [mouse line], the cortical layer (1, 2/3, 4, 5, 6a, 6b), and the Cell Reporter (Positive or Negative). By
, only a sub-set of these cells are listed; however, you can alter the sub-set of cells represented by clicking on the "More Options+" link and selecting from categories that include "Hemisphere", "Dendrite Type", "Apical Dendrite", "Morphology", and "Models".
The [#Cell Location] viewer is integrated with the [#Parallel Coordinates Plot] and the Cell Summaries list of experimental results, and enables
sorting and coloring
by the electrophysiological or morphological [features]. Features to sort and color by include: Upstroke:Downstroke, Adaptation, Rheobase, Membrane Time Constant (Tau), Firing Rate, Input Resistance, Normalized Cortical Depth, Max Distance and # of Stems.
Clicking "Reset Filters" will return the settings to the default parameters.
Whole-cell current clamp recordings were made from cells expressing the fluorescent molecule tdTomato (Reporter Positive) or from nearby non-florescent (Reporter Negative) cells. Fluorescent cells were Cre-positive cells from one of the transgenic lines described below. Whole-brain transgenic characterization of each Cre-line is available from the links below. To select a specific mouse line(s) click on the row(s) understanding that the layer refers to the selectivity of the florescence and "Type" refers to the putative Excitatory or Inhibitory cell type.
Cux2-CreERT2-Enriched in cortical layers 2/3/4, thalamus, midbrain, pons, medulla and cerebellum. View transgenic characterization.
Nr5a1-Cre-Expressed in restricted populations within the hypothalamus (ventromedial hypothalamus), and in cortical layer 4. View transgenic characterization.
Scnn1a-Tg2-Cre-Reporter expression in sparse and/or restricted regions of cortex (layer 4), thalamus, midbrain, medulla, pons, and cerebellum. View transgenic characterization.
Rorb-IRES2-Cre-Strong expression in the zonal layer of the superior colliculus and subregions of thalamus. Dense, patchy expression in layer 4 and sparse expression in layer 5 and 6 in cortex. Also expressed in trigeminal nucleus and small patches of cells in cerebellum. View transgenic characterization.
Scnn1a-Tg3-Cre-Enriched in cortical layer 4 and in restricted populations within cortex, thalamus, and in cerebellum. View transgenic characterization.
Rbp4-Cre_KL100-Enriched in cortical layer 5 and the dentate gyrus. View transgenic characterization.
Ntsr1-Cre_GN220-Specific to cortical layer 6 neurons. View transgenic characterization.
Slc17a6-IRES-Cre-Widespread expression throughout most of the brain, except very sparse expression in the striatum and restricted populations within cerebellum, medulla, and pons. View transgenic characterization.
Pvalb-IRES-Cre-Expressed in restricted and/or sparse populations within the cerebellum, medulla, pons, midbrain, cortex, hippocampus, thalamus, and striatum. View transgenic characterization.
Sst-IRES-Cre-Strong scattered expression throughout the brain. Localized areas of enrichment include restricted populations in thalamus, amygdala, midbrain, hindbrain, cortical subplate, and Purkinje cell layer. View transgenic characterization.
Htr3a-Cre_NO152-Reporter expression is detected in a subset of cortical interneurons. Enrichment is also detected in restricted populations within olfactory areas, pallidum, hypothalamus, pons, medulla, and cerebellum. View transgenic characterization.
Gad2-IRES-Cre-Specific to GABAergic neurons. Enriched in the striatum, piriform cortex, and within restricted populations in the thalamus, hypothalamus, cerebellum, olfactory areas, and GABAergic interneurons of the cortex. View transgenic characterization.
Cells were registered to the Allen Mouse Common Coordinate Framework (see whitepaper in "Documentation") and are illustrated in the approximate location on the representation of the visual cortical areas (see image below). Cell locations in 2-D are represented in the center image view (from a perspective above the brain) and are annotated: VISp - primary visual area, VISpl - visual area posterolateral, VISpor - [?], VISli - [?], VISl - visual area lateral, VISal - visual area anterolateral, VISrl - [?], VISa - visual area [?], VISam - visual area anteromedial, VISpm - visual area posteromedial and RSPagl - retrosplenial area, lateral agranular part. The cortical depth of the cell is indicated in either the coronal or the saggital view, shown in the bottom and side views, respectively. The coronal and saggital views are labeled with the Pia (top of the brain), the White Matter (or bottom of the cortex) as well as the Lateral (L), Medial (M), Rostral (R) or Caudal (C) aspects of the brain.
Filtering the cells (using the [#Filters] parameters or the sliders in the [Parallel Coordinate Plot]) will result in a decrease or increase in the number of cells visualized on this map.
Once you hover your mouse over a cell, the cell will be outlined in black and meta-data for that cell will be displayed in the upper left hand corner of the map.
Quick Electrophysiological or Morphological searches are available by clicking on those headings above the map.
A fraction of the cells that were selected for imaging and reconstruction (see Morphology Overview whitepaper in Documentation for more details) showed enough morphological similarities that a curated search based on these features is available from the dropdown above the Cell Location map. To find similar cells based on Normalized Cortical Depth and Mouse Line, click on the average morphology thumbnail to pull up a list of cells that fit that criteria. Note: the number of cells that fit the criteria is listed in the title banner of the Filters box.
A fraction of cells with well-characterized electrophysiological properties (see Electrophysiology Overview whitepaper in Documentation for more details) have been selected for a curated search. These searches select for cell types with regular to moderate to fast spiking rates with unique adaptation or time constant parameters. To select the cells with these characteristics, click on the image. Note: the number of cells that fit the criteria is listed in the title banner of the Filters box.
Another way to visualize this data, which has many distinct and sometimes unrelated dimensions, is a Parallel Coordinate Plot. This visualization plots each cell according to a finite number of electrophysiological and/or morphological features.
When you have selected the Electrophysiology Mode from the Filters box, six features are illustrated in the Parallel Coordinate Plot: Upstroke/Downstroke Ratio, Adaptation Index, Rheobase, Membrane Time Constant (Tau) and Input Resistance. When the "Electrophysiology + Morphology" mode is instead selected, again six features are shown: three electrophysiology features; Upstroke/Downstroke Ratio, Adaptation Index and Rheobase, as well as three Morphology features: Normalized Cortical Depth, Max Distance and # Stems.
You can limit your search by using the slider bars on each axis. Hovering your mouse over the axis of the parameter you are interested in inspecting will illuminate the data included in your search. Click and drag from the extremes of the axis to limit your search.
Each of the axes can be relocated by clicking and dragging the title to another position along the x-axis.
While many distinct electrophysiological features were recorded and/or calculated from each cell, only a few features were called out in the web application. To see the other features, please read the Electrophysiology Overview whitepaper in the "Documentation" tab and/or download the data from the Allen Brain Atlas API. These features were selected not only by what they were able to tell us about the intrinsic properties of the cells, but also in their ability to differentiate between putative cell types in a non-biased clustering analysis.
The ratio between the absolute values of the action potential peak upstroke and the action potential peak downstroke. Action potential peak upstroke: The maximum rate of change between the action potential threshold and the action potential peak. Action potential peak downstroke: The minimum rate of change between the action potential peak and the action potential trough.
This value gives us an indication of the amount of time a cell takes to recover after an Action Potential. An example of the difference between a high and a low ratio is illustrated here.
This parameter is used to distinguish between spiny (putatively excitatory) and aspiny (putatively inhibitory) groups of cells in a non-biased clustering analysis.
Not only are isolated action potentials of interest, but the rates of firing are likely to be important in intra-neuron communication. The adaptation index is the rate at which action potential firing changes during a stimulus. This index is used to characterize a neurons response to a sustained input, a one second square pulse in this case.
A high adaptation index means the neuron spikes at the beginning of the stimulus, but then stops spiking. These neurons transmit the initiation of an upstream input. Conversely, a neuron that does not accommodate (has a low Adaptation index) gives a consistent output during the sustained input and can be used to tell when a stimulus ends. The adaptation index likely involves ion channel proteins that change properties on the time scale of hundreds of milliseconds to seconds.
This value is the amount of stimulus current (long square current in pA) required to initiate a single action potential. This parameter gives us an indication of the excitability and the membrane resistance of the cell.
The membrane time constant, also referred to as tau, is the speed at which a neuron charges it's membrane. This is one of the passive or subthreshold properties of the cell and is the product of the [input resistance] and the cell capacitance. The cell capacitance is determined by injecting brief subthreshold square currents (see "Square 0.5 ms Subthreshold" [stimulus]). The cell’s capacitance is closely related to the amount of membrane the cell has, a larger membrane giving a higher capacitance. This feature determines how responsive a neuron is to a given stimulus at baseline.
The firing rate is simply the speed at which a neuron fires multiple action potentials in sequence given a sustained current injection. A neuron that fires at a faster rate could influence a downstream neuron more strongly than a neuron firing with a slower rate. The rate that a neuron fires given a sustained input is determined by the ion channel proteins it expresses and whether and how fast those ion channel proteins recover from the previous action potential. In general, a higher firing rate is seen in neurons that spike faster and have a deeper after hyperpolarization. This is illustrated in the [parallel coordinate plot] where cells with a greater Upstroke/Downstroke ratio show a lower firing rate.
The input resistance is the baseline resistance of the neuron membrane, and like [tau] is one of the passive or subthreshold properties of the cell. A cell with high input resistance leads to a large voltage response (Nernst equation: V=IR) and is referred to as "tight" as current doesn't easily leak out. Conversely "leaky" neurons are those with low input resistance. The input resistance was calculated by measuring the slope of the V/I plot at subthreshold potentials.
A sub-set of cells with electrophysiological recordings was manually selected to enter our 3-D reconstruction pipeline. Similar to the electrophysiology features, many morphology features were calculated in the reconstruction, but only three are called out in the web application; Normalized Cortical Depth, Max Distance and # Stems. To see the entire array of morphological features, please read the Morphology Overview whitepaper in "Documentation" or download the data from the Allen Brain Atlas API.
The three features represented in the web application were the top three most discriminative features (ranked by a classic machine learning technique) that best separates major morphological categories of neurons currently included in the database. These morphology categories are some of the most common in this dataset.
This is the maximum
of all the nodes. Euclidean distance is the straight line distance from the soma (root) to the node. The maximum euclidean distance is able to distinguish a particular category of spiny neuron ("tall, tufted") from a particular category of aspiny neuron ("common type").
number of stems
attached to the soma. The # Stems is used to distinguish between two categories of spiny neurons (“star pyramid” versus “tufted”).
Filtering of the dataset results in a list of experiments ranked (by default) by Upstroke:Downstroke. You can alter the sort parameters from the [#Filters] menu.
Each experiment lists meta-data regarding the classification of the cell, including the Cre-line, the Area, the Layer, Cell Reporter (positive or negative), the Dendrite Type as well as whether or not the Apical Dendrite is intact. It also includes thumbnails showing the electrical traces,I STOPPED HERE.
If you have selected several cells to compare, you can save this or other kinds of searches by selecting the "Permalink" feature.
Clicking anywhere in a cell's results box will open a new page with the experimental details.
The Experimental Detail page includes the Electrophysiological Summary and a workspace to Browse the Electrophysiology Data. The Electrophysiology Summary includes images of the cell and the location of the cell mapped to the CCF, meta-data on the Mouse Line and location of the cell, as well as the [cell features] most appropriate to the search parameters. It also includes model fit parameters (where appropriate). You can also view plots of the F/I and V/I curves here.
Clicking on the image of the cell will open a new page containing the [#Morphology] data.
The electrophysiological data itself can be viewed from this page, or [downloaded] to be visualized on another platform or in a third party program. The Allen SDK provides a simple Python module to support downloading metadata and NWB files for cells in the Allen Cell Types Database. Please see the Data API Client documentation page to see an example.
- Select Stimulus type: A drop-down menu from which you can select the [stimulus type] and see the resulting Cell Response.
- Select Neuronal Model: When available, [neuronal models] have been run on the data and when selected will open below the recorded Cell Response.
- Download Data: This link will download the .nwb file with the data from this experiment. For more information, please see here.
- Select Sweep: Select sweeps will be available for you to inspect from this view. As you hover your mouse over each colored square, not only do you see the resulting graphs change to reflect the sweep selected, but you also will see sweep meta-data (Sweep #, Stimulus amplitide (pA) and # of spikes) listed below the squares. Once you click on a colored square, you can use left/right arrow keys to move between the sweeps.
- Slider Bar: This feature allows you to zoom in and out of the Stimulus, Cell Response and Model views by clicking and dragging on the arrows.
- Stimulus: The stimulus injected into the cell.
- Cell Response: The response of the cell to the injected stimulus.
- (Optional) Model Response: When available, the model of the cellular response.
Different sets of stimulation waveforms were used in order to:
- Interrogate intrinsic membrane mechanisms that underlie the input/output function of neurons
- Linear and non-linear subthreshold properties
- Action potential initiation and propagation
- Understand aspects of neural response properties in vivo
- Stimulation frequency dependence (theta vs. gamma) of spike initiation mechanisms
- Ion channel states due to different resting potentials in vivo
- Construct and test computational models of varying complexity emulating the neural response to stereotyped stimuli
- Generalized leaky-integrate-and-fire (GLIF) models
- Biophysically and morphologically realistic conductance-based compartmental models
The data since the 2015 release has been re-processed, so if you used the models last year, run it again with the new ones.
The Allen Cell Types Database contains two types of neuronal models: perisomatic biophysical models and generalized leaky integrate-and-fire (GLIF) models. These models attempt to mathematically reproduce a cell's recorded response to a current injection. The perisomatic biophysical models take into account dendritic morphological structure, whereas GLIF models are simple point neuron models which represent the neuron as a single compartment.
There are five levels of GLIF models with increasing levels of complexity. The most basic model is a simple leaky integrate-and-fire equation. More advanced GLIFs attempt to model variable spike threshold, afterspike currents, and threshold adaptation.
More detailed information on each of the models is available in the whitepapers in Documentation.
1. Leaky Integrate and Fire (LIF)
Standard circuit representation of a resistor and capacitor in parallel with a leaky membrane.
2. LIF + Reset Rules (LIF-R)
LIF with biologically-derived threshold and voltage reset rules in addition to a biologically derived threshold decay.
3. LIF + Afterspike Currents (LIF-ASC)
LIF with spike-induced currents to model long-term effects of voltage-activated ion channels.
4. LIF-R + Afterspike Currents (LIF-R-ASC)
LIF with additional Reset Rules and Afterspike Currents.
5. LIF-R-ASC + Threshold Adaptation (LIF-R-ASC-A)
All of the above, with an additional voltage-dependent component of threshold.
Models with active conductances at the soma and passive dendritic morphology based on full 3-D reconstruction.
When available: the Morphology page can be reached either by clicking on the image of the reconstructed cell in the search results page,
or by clicking on the image of the cell on the Electrophysiological Detail Page.
The Experimental Detail page includes the Morphology Summary and a workspace to Browse the Morphology Data. The Morphology Summary includes the location of the cell mapped to the CCF, meta-data on the Mouse Line and location of the cell, as well as the Morphological features most appropriate to the data (see more information in the Morphology whitepaper in Documentation).
Clicking on the image of the cell trace will open a new page containing the [#Electrophysiology Results] data.
Projected views of the biocytin filled neuron were constructed by composing the darkest intensity pixel from each plane of the image stack into a single plane.
Projected top view and side view, as well as the 3-D neuron reconstruction can be viewed from this page
From the Projected top view, you can zoom into the picture from the on-screen navigation tools, the [#Keyboard Commands] or using your scroll wheel. The two views of the neuron are synched so zooming in on one will also zoom the other. Clicking on "View image stack" will take you to an [image viewer] to view the individual images taken of this neuron.
The image viewer of the 3-D neuron reconstruction allows for visualization of the reconstructed neuron using the onscreen navigation tools. Clicking "Front" will reset the neuron to it's default view.
You can download both the reconstruction (as an .swc file) or the calculated morphological measurements (as an XML) from the links below the viewers. For more information please see the API Documentation.
Clicking "View Image Stack" while browsing the Morphology data will take you to our image viewer. The title bar includes the Mouse Line, the Specimen ID, the location from which the cell came as well as a menu that will allow you to vary the image contrast and download the individual images. The entire image stack can be navigated through using the on screen navigation tools, using the [#Keyboard Commands] or by clicking on the Projected Side View.
Shows the current viewing resolution of the image, in microns. This value dynamically changes as you zoom in/out of the image. You can position the scale bar anywhere on the main image by dragging the scale bar by its ruler.
You can toggle the orientation of the scale bar from horizontal to vertical by clicking on the scale bar text.
Advance to the next image from the specimen
Go back to the previous image from the specimen