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Potential window for treating ALS identified

Date:
March 29, 2022
Source:
Johns Hopkins Medicine
Summary:
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder that affects as many as 30,000 people in the United States, with 5,000 new cases diagnosed each year. It weakens muscles over time, impacting physical function and ultimately leading to death. There is no single cause for the disease and no known cure. However, researchers have found a possible window of opportunity during ALS treatment to target astrocyte abnormalities.
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Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder that affects as many as 30,000 people in the United States, with 5,000 new cases diagnosed each year. It weakens muscles over time, impacting physical function and ultimately leading to death. There is no single cause for the disease and no known cure. However, Johns Hopkins Medicine researchers have found a possible window of opportunity during ALS treatment to target astrocyte abnormalities -- a subtype of cells in the central nervous system that provide a structure to metabolically support neurons and fine-tune neuron network signaling.

The research team believes that astrocytes are actively involved in the death of motor neurons, which are cells in the brain and spinal cord that allow people to move, speak, swallow and breathe by sending commands from the brain to the muscles that carry out these functions.

"We think this is particularly important because the astrocyte dysfunction is active after symptom onset in patients with ALS," says Nicholas Maragakis, M.D., professor of neurology at the Johns Hopkins University School of Medicine and medical director of the Johns Hopkins ALS clinical trials unit. "This finding may enable us to target abnormalities in astrocytes for ALS treatment."

In their study, published March 21 in the Proceedings of the National Academy of Sciences, researchers analyzed brain and spinal cord tissues from patients with ALS and observed that a particular astrocyte protein, connexin 43, acts as an open pore that sends toxic factors to the motor neurons from the astrocytes. The pore was particularly active in patients with ALS who have a family history of the disease and those who contracted the disease in a sporadic fashion.

The research team was also able to develop stem cell lines from patients with ALS and develop them into astrocytes. They found that these astrocytes induced motor neuron death through hemichannels (proteins that provide pathways for the movement of molecules among cells).

"This is a new pathway that we have shown to be present in ALS tissues, animal models and patient-derived stem cells," Maragakis says. "It's also exciting that this particular hemichannel protein seems to be elevated in spinal fluid from patients with ALS and could serve as an important biomarker. This is a true precision medicine approach toward the disease."

Maragakis says pharmaceuticals are being developed that could block this hemichannel. During the study, his team showed that tonabersat, a drug originally developed for treatment of migraine and epilepsy, could block astrocyte-induced motor neuron death in human ALS stem cell lines and animal models.

This study, Maragakis says, offers increasing evidence that astrocytes play a role in the spread of ALS. Next, the team will try to establish why this hemichannel is so active in ALS astrocytes, giving them a better understanding of how the disease progresses. Maragakis says it's equally important because it furthers his team's work to identify new drugs that can block this particular hemichannel, serving as future therapeutics for ALS.

The study was funded by the ALS Association, the Maryland Stem Cell Research Fund, the Robert Packard Center for ALS Research at Johns Hopkins, the U.S. Department of Defense and the National Institutes of Health.


Story Source:

Materials provided by Johns Hopkins Medicine. Note: Content may be edited for style and length.


Journal Reference:

  1. Akshata A. Almad, Arens Taga, Jessica Joseph, Sarah K. Gross, Connor Welsh, Aneesh Patankar, Jean-Philippe Richard, Khalil Rust, Aayush Pokharel, Caroline Plott, Mauricio Lillo, Raha Dastgheyb, Kevin Eggan, Norman Haughey, Jorge E. Contreras, Nicholas J. Maragakis. Cx43 hemichannels contribute to astrocyte-mediated toxicity in sporadic and familial ALS. Proceedings of the National Academy of Sciences, 2022; 119 (13) DOI: 10.1073/pnas.2107391119

Cite This Page:

Johns Hopkins Medicine. "Potential window for treating ALS identified." ScienceDaily. ScienceDaily, 29 March 2022. <www.sciencedaily.com/releases/2022/03/220329090727.htm>.
Johns Hopkins Medicine. (2022, March 29). Potential window for treating ALS identified. ScienceDaily. Retrieved March 27, 2024 from www.sciencedaily.com/releases/2022/03/220329090727.htm
Johns Hopkins Medicine. "Potential window for treating ALS identified." ScienceDaily. www.sciencedaily.com/releases/2022/03/220329090727.htm (accessed March 27, 2024).

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