With the current launch of the Allen Cell Types Database, we include electrophysiological recordings from over 800 individual cells, a subset 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) select 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, 6), and the Cell Reporter (Positive or Negative). By default, only a subset of these cells are listed; however, you can alter the subset 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 Coordinate Plot and the Cell Summaries list of experimental results, and enables
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imagelinktestby 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 Number 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-fluorescent (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 fluorescence 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.
Ctgf-2A-dgCre-Cre expression is restricted to layer 6b of cortex and in restricted populations within cortical subplate. 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.
Vip-IRES-Cre-Strong scattered expression throughout the brain. Enriched expression in superficial cortical layers and restricted populations in hindbrain and midbrain. 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 according to Wang and Burkhalter (J. Comp. Neurol., 502: 339--357. doi: 10.1002/cne.21286).
The cortical depth of the cell is indicated in either the coronal or the sagittal view, shown in the bottom and side views, respectively. The coronal and sagittal 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.
Primary Visual Area
Posterolateral visual area
Lateral visual area
Anterolateral visual area
Rostrolateral visual area
Anteromedial visual area
Posteromedial visual area
Retrosplenial area, lateral agranular part
Filtering the cells (using the #Filters parameters or the sliders in the Parallel Coordinate Plot) will result in a change 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 metadata 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 Morphology link 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 and are available by clicking on the Electrophysiology link from above the Cell Location map. These searches select 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 inter-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 the spiking slows or stops altogether. These neurons therefore are likely 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 might also 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, reflects the time it takes for a neuron to charge its 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 membrane time constant in this study was estimated by fitting voltage responses to negative current injection with an exponential.
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 with individual action potentials that are more narrow 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 (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 subset of cells with electrophysiological recordings was manually selected for 3-D reconstruction. 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.
As the thickness of the visual cortex changes naturally and can also be affected by non-biological factors like tissue shrinkage during histology, we compute the relative depth of the soma with respect to the pia and white matter using the cortical coordinate space in the CCF (see whitepaper in Documentation).
This is the maximumof 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").
Theattached 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 metadata 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 a trace of the action potential from which many of the electrophysiological features are calculated and (when available) the reconstructed neuron.
The thumbnail depicting the reconstructed neuron includes the dendrites (red), the apical dendrites (orange) and the axon (blue). The portion of the neuron representing each of these morphologies is depicted in a histogram to the right of the reconstructed neuron. The neurons location in the cortex is indicated by the scale showing normalized cortical depth where the top is the pial surface and the bottom is the white matter. NOTE: this scale is not a measure of cortical layer.
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 Electrophysiology Data. The Electrophysiology Summary includes a thumbnail of the location of the cell mapped to the CCF, metadata on the cell including Mouse Line, ID, Area, Cell Reporter, Dendrite Type, Apical Dendrite and Hemisphere. Values from each of the electrophysiology cell features are also listed along with model parameters (where appropriate). You can also view plots of the F/I and V/I curves here.
Clicking on the image of the cell (when available) 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.
Different sets of stimulation waveforms were used in order to:
Reprocessing of the data occurred for the March 2016 release so any analysis performed prior to the March 2016 release date should be performed again with the new models.
The Allen Cell Types Database contains three types of neuronal models: two 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 biophysical models take into account dendritic morphological structure, whereas GLIF models are simple point neuron models that 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.
Biophysically realistic, single-neuron model with passive dendrites and active soma.
Biophysically realistic, single-neuron model with active conductances everywhere.
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 viewer to browse the morphology data. The Morphology Summary includes the location of the cell mapped to the CCF, metadata on the Mouse Line and location of the cell. It also shows the Morphological features most appropriate to the data (see more information in the Morphology whitepaper in Documentation), a thumbnail showing the neuron reconstruction including cortical depth, as well as a thumbnail illustrating the electrophysiology traces.
Clicking on the electrophysiology thumbnail 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 "Reset" will reset the neuron to its default view. The legend in the 3D reconstruction indicates the various components of the reconstruction.
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 structure and the hemisphere. The "Configure" icon opens 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