STUDY IDENTIFIES FEATURES THAT MAY MAKE MOTOR NEURONS VULNERABLE TO ALS

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U.S. Department of Health and Human Services
NATIONAL INSTITUTES OF HEALTH NIH News
National Institute of Neurological Disorders and Stroke (NINDS) <http://www.ninds.nih.gov/>
For Immediate Release: Thursday, February 2, 2023

CONTACT: Erin Bryant, 301-496-5751, <e-mail:NINDSPressTeam@xxxxxxxxxxxxx>

MEDIA ADVISORY

STUDY IDENTIFIES FEATURES THAT MAY MAKE MOTOR NEURONS VULNERABLE TO ALS
Human spinal cord cell atlas provides foundation to study neurodegeneration, chronic pain, and other diseases

What:
New research offers clues about the biology of cells in the spinal cord that die off in amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases. A team of researchers supported by the National Institutes of Health found evidence linking motor neurons' large cell size and supporting structure with the genes that underlie their vulnerability to degeneration in ALS. Findings appeared in Neuron.

The study resulted in a catalog or "atlas" characterizing the diverse community of cell types within the human spinal cord. By examining gene expression at the single-cell level, the researchers identified dozens of cell types in the spinal cord and analyzed their molecular profiles. They demonstrated the usefulness of the atlas by looking closely at motor neurons, which provide voluntary movement and motor control. Motor neurons, which degenerate and die in ALS, are large cells with one long extension called an axon―up to a meter long―that conducts signals from the spinal cord to the muscle fiber.

The team found that motor neurons are distinguished by a set of genes that may enable the large size of the motor neuron cell body and lengthy axon, but also underlie their vulnerability to degeneration. Their molecular profile was defined by genes involved in cytoskeletal structure, which gives the cell shape and organizes the structures within; neurofilament genes related to cell size; and genes linked to the onset of ALS. Additional experiments showed that ALS-related genes are also enriched in motor neurons in mice. Taken together, the study gives insight into ALS and demonstrates the utility of the spinal cell atlas to study disease and possible interventions.

WHO:
Ariel Levine, M.D., Ph.D., Principal Investigator, National Institute of Neurological Disorders and Stroke (NINDS). To arrange an interview, please contact NINDSPressTeam@xxxxxxxxxxxxx.

ARTICLE:
Yadav, et al. A Cellular Taxonomy of the Adult Human Spinal Cord. 2023 Feb 1. Neuron. DOI: 10.1016/j.neuron.2023.01.007

NINDS is the nation's leading funder of research on the brain and nervous system. The mission of NINDS is to seek fundamental knowledge about the brain and nervous system and to use that knowledge to reduce the burden of neurological disease.

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