Summary: Combining two-photon fluorescent microscopy and all-optical laser scanning, researchers can image the brain of an alert mouse 1,000 times a second, recording the passage of millisecond electrical pulses through neurons.
Source: UC Berkeley
Electrical and chemical signals flash through our brains constantly as we move through the world, but it would take a high-speed camera and a window into the brain to capture their fleeting paths.
University of California, Berkeley, investigators have now built such a camera: a microscope that can image the brain of an alert mouse 1,000 times a second, recording for the first time the passage of millisecond electrical pulses through neurons.
“This is really exciting, because we are now able to do something that people really weren’t able to do before,” said lead researcher Na Ji, a UC Berkeley associate professor of physics and of molecular and cell biology.
The new imaging technique combines two-photon fluorescence microscopy and all-optical laser scanning in a state-of-the-art microscope that can image a two-dimensional slice through the neocortex of the mouse brain up to 3,000 times per second. That’s fast enough to trace electrical signals flowing through brain circuits.
With this technique, neuroscientists like Ji can now clock electrical signals as they propagate through the brain and ultimately look for transmission problems associated with disease.
One key advantage of the technique is that it will allow neuroscientists to track the hundreds to tens of thousands of inputs any given brain cell receives from other brain cells, including those that don’t trigger the cell to fire. These sub-threshold inputs — either exciting or inhibiting the neuron — gradually add up to a crescendo that triggers the cell to fire an action potential, passing information along to other neurons.
From electrodes to fluorescence imaging
The typical method for recording electrical firing in the brain, via electrodes embedded in the tissue, detects only blips from a few neurons as the millisecond voltage changes pass by. The new technique can pinpoint the actual firing neuron and follow the path of the signal, millisecond by millisecond.
“In diseases, many things are happening, even before you can see neurons firing, like all the subthreshold events,” said Ji, a member of UC Berkeley’s Helen Wills Neuroscience Institute. “We’ve never looked at how a disease will change with subthreshold input. Now, we have a handle to address that.”
Ji and her colleagues reported the new imaging technique in the March issue of the journal Nature Methods. In the same issue, she and other colleagues also published a paper demonstrating a different technique for imaging calcium signaling over much of an entire hemisphere of the mouse brain at once, one that uses a wide-field-of-view “mesoscope” with two-photon imaging and Bessel focus scanning. Calcium concentrations are linked with voltage changes as signals are transmitted through the brain.
When a neuron fires, calcium flows into the cell in a wave that sweeps along the cell body. Images of this infragranular neuron were obtained three times per second by two-dimensional scanning with a Bessel focus. Redder structures are deeper in the mouse cortex. Credit: UC Berkeley.
“This is the first time anyone has shown in three dimensions the neural activity of such a large volume of the brain at once, which is far beyond what electrodes can do,” Ji said. “Furthermore, our imaging approach gives us the ability to resolve the synapses of each neuron.”
Synapses are the spots where neurotransmitters are released by one neuron to excite or inhibit another.
One of Ji’s goals is to understand how neurons interact across large areas of the brain and eventually locate diseased circuits linked to brain disorders.
“In brain disorders, including neurodegenerative disease, it’s not just a single neuron or a few neurons that get sick,” Ji said. “So, if you really want to understand these illnesses, you want to be able to look at as many neurons as possible over different brain regions. With this method, we can get a much more global picture of what is happening in the brain.”
Ji and her colleagues are able to peer into the brain thanks to probes that can be pinned to specific types of cells and become fluorescent when the environment changes. To track voltage changes in neurons, for example, her team employed a sensor developed by co-author Michael Lin of Stanford University that becomes fluorescent when the cell membrane depolarizes as a voltage signal propagates along the cell membrane.
The researchers then illuminate these fluorescent probes with a two-photon laser, which makes them emit light, or fluoresce, if they have been activated. The emitted light is captured by a microscope and combined into a 2D image that shows the location of the voltage change or the presence of a specific chemical, such as the signaling ion, calcium.
By rapidly scanning the laser over the brain, much like a flashlight that gradually reveals the scene inside a darkened room, researchers are able to obtain images of a single, thin layer of the neocortex. The team was able to conduct 1,000 to 3,000 full 2D scans of a single brain layer every second by replacing one of the laser’s two rotating mirrors with an optical mirror — a technique called free-space angular-chirp-enhanced delay (FACED). FACED was developed by paper co-author Kevin Tsia at the University of Hong Kong.
The kilohertz imaging not only revealed millisecond changes in voltage, but also more slowly changing concentrations of calcium and glutamate, a neurotransmitter, as deep as 350 microns (one-third of a millimeter) from the brain’s surface.
To obtain rapid 3D images of the movement of calcium through neurons, she combined two-photon fluorescent microscopy with a different technique, Bessel focus scanning. To avoid time-consuming scans of every micron-thick layer of the neocortex, the excitation focus of the two-photon laser is shaped from a point to a small cylinder, like a pencil, about 100 microns in length. This pencil beam is then scanned at six different depths through the brain, and the fluorescent images are combined to create a 3D image. This allows more rapid scanning with little loss of information because in each pencil-like volume, typically only one neuron is active at any time. The mesoscope can image an area about 5 mm in diameter — nearly a quarter of one hemisphere of the mouse brain — and 650 microns deep, close to the full depth of the neocortex, which is involved in complex information processing.
Waves of calcium flowing through neurons. Credit: Na Ji/UC Berkeley.
“Using conventional methods, we would have to scan 300 images to cover this volume, but with an elongated beam that collapses the volume onto a single plane, we only need to scan six images, which means that now we can have a fast enough volumetric rate to look at its calcium activity,” Ji said.
Ji is now working on combining four techniques — two-photon fluorescence microscopy, Bessel beam focusing, FACED and adaptive optics — to achieve high-speed, high sensitivity images deep in the neocortex, which is about 1 millimeter thick.
“As a way to understand the brain, my dream is to combine these microscopy techniques to get submicron spatial resolution so we can see the synapses, millisecond time resolution for the voltage imaging, and see all of this deep in the brain,” she added. “What is complicated and challenging about the brain is that, if you only do one single optical section, in a way you don’t get a complete picture, because a neural network is very much three-dimensional.”
Co-authors on the voltage imaging paper with Ji, Lin and Tsia are Jianglai Wu and Shuo Chen of UC Berkeley, Yajie Liang and Ching-Lung Hsu of the Howard Hughes Medical Institute (HHMI) Janelia Research Campus in Virginia, and Mariya Chavarha, Stephen Evans and Dongqing Shi of Stanford.
Co-authors with Ji on the calcium imaging paper are co-first authors Rongwen Lu and Yajie Liang of Janelia and Guanghan Meng of UC Berkeley; Pengcheng Zhou and Liam Paninski of Columbia University; and Karel Svoboda of Janelia.
Funding: Ji’s work is supported by HHMI and the National Institute of Neurological Disorders and Stroke of the National Institutes of Health (U01NS103489, UF1NS107696).
About this neuroscience research article
Source: UC Berkeley Media Contacts: Robert Sanders – UC Berkeley Image Source: The image is credited to Na Ji.
Kilohertz two-photon fluorescence microscopy imaging of neural activity in vivo
Understanding information processing in the brain requires monitoring neuronal activity at high spatiotemporal resolution. Using an ultrafast two-photon fluorescence microscope empowered by all-optical laser scanning, we imaged neuronal activity in vivo at up to 3,000 frames per second and submicrometer spatial resolution. This imaging method enabled monitoring of both supra- and subthreshold electrical activity down to 345 μm below the brain surface in head-fixed awake mice.
Rapid mesoscale volumetric imaging of neural activity with synaptic resolution
Imaging neurons and neural circuits over large volumes at high speed and subcellular resolution is a difficult task. Incorporating a Bessel focus module into a two-photon fluorescence mesoscope, we achieved rapid volumetric imaging of neural activity over the mesoscale with synaptic resolution. We applied the technology to calcium imaging of entire dendritic spans of neurons as well as neural ensembles within multiple cortical regions over two hemispheres of the awake mouse brain.