A microscope about the size of a penny is giving scientists a new window into the everyday activity of cells within the spinal cord. The innovative technology revealed that astrocytes–cells in the nervous system that do not conduct electrical signals and were traditionally viewed as merely supportive–unexpectedly react to intense sensation.
The new miniaturized microscope and related imaging methods, described by Salk Institute scientists on April 28, 2016 in Nature Communications, offer unprecedented insight into nervous system function and could lead to novel pain treatments for spinal cord injuries, chronic itch and neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS).
The spinal cord is crucial for sensing and responding to the world. Sometimes it even works independently from the brain, such as when your hand recoils from a hot stove before the sensation has fully registered. But it is unknown exactly how the cells within the spinal cord encode these and other feelings from the skin or internal organs.
In the new study, senior author Axel Nimmerjahn, an assistant professor in Salk’s Waitt Advanced Biophotonics Center, and his team improved upon the miniaturized microscopes they first described back in 2008. The researchers’ new version–which features numerous hardware and software improvements–enabled them to visualize changes in cellular activity in awake, roaming mice.
“For a long time, researchers have dreamed of being able to record cellular activity patterns in the spinal cord of an awake animal. On top of that, we can now do this in a freely behaving animal, which is very exciting,” says first author Kohei Sekiguchi, a Salk researcher and PhD student at the University of California, San Diego.
Most of the Salk team’s previous work focused on deploying microscopes to observe the brains of living animals. The spinal cord, by contrast, presented a bigger challenge for several reasons. For example, unlike the brain, multiple, independently moving vertebrae surround the spinal cord. The spinal cord is also closer to pulsating organs (heart and lungs), which can hinder stable views of the cells within. However, by developing new microscopy and procedural and computational approaches, the team was able to overcome these challenges and capture the action of living cells in real time and during vigorous movements.
In the new work, the group found that distinct stimuli–such as light touch or pressure–activate different subsets of spinal sensory neurons. They also found that certain features, like the intensity or duration of a given stimulus, are reflected in the activity of the neurons.
To the team’s surprise, astrocytes, traditionally thought to be passive support cells, also respond to stimuli (albeit differently than the neurons). Though the astrocytes cannot send electrical signals like neurons can, they generated their own chemical signals in a coordinated way during intense stimuli.
Nimmerjahn is excited about this result because his group has a longstanding interest in understanding astrocytes and their roles in nervous system function and disease. These cells are increasingly appreciated as important players in how the nervous system develops and operates and could serve as promising new drug targets, he says.
“Not only can we now study normal sensory processing, but we can also look at disease contexts like spinal cord injury and how treatments actually affect the cells,” says Nimmerjahn.
The team is now working to simultaneously record touch or pain-related activity in the brain and spinal cord using additional iterations of the miniaturized microscopes, which allow them to monitor and manipulate multiple cell types at even higher resolutions.
About this genetics research
Other researchers on the paper include the Salk Institute’s Pavel Shekhtmeyster, Katharina Merten, Alexander Arena, Daniela Cook, Elizabeth Hoffman and Alexander Ngo.
Funding: The work was supported by grants from the National Institutes of Health, the Rita Allen Foundation, Whitehall Foundation and Brain Research Foundation; funds from the Waitt Foundation, Hearst Foundations and the Richard Allan Barry Family Charitable Foundation; and research fellowships from the Nakajima Foundation, Mary K. Chapman Foundation, Jesse and Caryl Philips Foundation, the Rose Hills Foundation, Deutsche Forschungsgemeinschaft (DFG) and the Catharina Foundation.
Source:Salk Institute Image Credit: The image is credited to Salk Institute. Video Source: The video is credited to Salk Institute. Original Research: Full open access research for “Imaging large-scale cellular activity in spinal cord of freely behaving mice” by Kohei J. Sekiguchi, Pavel Shekhtmeyster, Katharina Merten, Alexander Arena, Daniela Cook, Elizabeth Hoffman, Alexander Ngo and Axel Nimmerjahn in Nature Communications. Published online April 28 2016 doi:10.1038/ncomms11450
Imaging large-scale cellular activity in spinal cord of freely behaving mice
Sensory information from mechanoreceptors and nociceptors in the skin plays key roles in adaptive and protective motor behaviours. To date, very little is known about how this information is encoded by spinal cord cell types and their activity patterns, particularly under freely behaving conditions. To enable stable measurement of neuronal and glial cell activity in behaving mice, we have developed fluorescence imaging approaches based on two- and miniaturized one-photon microscopy. We show that distinct cutaneous stimuli activate overlapping ensembles of dorsal horn neurons, and that stimulus type and intensity is encoded at the single-cell level. In contrast, astrocytes show large-scale coordinated calcium responses to intense but not weak sensory inputs. Sensory-evoked activity is potently suppressed by anaesthesia. By revealing the cellular and computational logic of spinal cord networks under behaving conditions, our approach holds promise for better understanding of healthy and aberrant spinal cord processes.
“Imaging large-scale cellular activity in spinal cord of freely behaving mice” by Kohei J. Sekiguchi, Pavel Shekhtmeyster, Katharina Merten, Alexander Arena, Daniela Cook, Elizabeth Hoffman, Alexander Ngo and Axel Nimmerjahn in Nature Communications. Published online April 28 2016 doi:10.1038/ncomms11450