Inhibitory interneuron, a type of neuron is primarily important to manage the brain rhythms. A new study led by Jorge Palop, PhD, assistant investigator at the Gladstone Institutes finds that genetically improving these interneurons and transplanting them into the brain of a mouse model of Alzheimer's disease will be able to restore the cognitive functions of the brain. The findings of the study are published in the journal Neuron .
Like a great orchestra, your brain relies on the perfect coordination of many elements to function properly. And if one of those elements is out of sync, it affects the entire ensemble. In Alzheimer's disease, for instance, damage to specific neurons can alter brainwave rhythms and cause a loss of cognitive functions.
Alzheimers Disease
Alzheimer''s disease is a progressive neurodegenerative disease affecting memory and thinking and making the person increasingly dependent on others.
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‘Inhibitory interneurons with enhanced function can be able to restore the brain functions.’
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Interneurons control complex networks between neurons, allowing them to send signals to one another in a harmonized way. You can think of inhibitory interneurons as orchestra conductors. They create rhythms in the brain to instruct the players--excitatory neurons--when to play and when to stop. An imbalance between these two types of neurons creates disharmony and is seen in multiple neurological and psychiatric disorders, including Alzheimer's disease, epilepsy, schizophrenia, and autism.
A Brain without a Conductor
Palop's previous studies showed that, in mouse models of Alzheimer's, the inhibitory interneurons do not work properly. So, the rhythms that organize the excitatory cells are disturbed and fail to function harmoniously, causing an imbalance in brain networks. This, in turn, affects memory formation and can lead to epileptic activity, which is often observed in patients with Alzheimer's disease.
![Healthy Mitochondria May Stop Alzheimer’s Disease]( "Healthy Mitochondria May Stop Alzheimer’s Disease")
Enhancing mitochondrial proteostasis reduces the formation of amyloid plaques and delays amyloid-beta proteotoxic diseases, such as Alzheimer's disease.
His team found a way to reengineer inhibitory interneurons to improve their function. They showed that these enhanced interneurons, when transplanted into the abnormal brain of Alzheimer mice, can properly control the activity of excitatory cells and restore brain rhythms.
"We took advantage of the fact that transplanted interneurons can integrate remarkably well into new brain tissues, and that each interneuron can control thousands of excitatory neurons," said Palop, who is also an assistant professor of neurology at the University of California, San Francisco. "These properties make interneurons a promising therapeutic target for cognitive disorders associated with brain rhythm abnormalities and epileptic activity."
First, the scientists had to overcome a significant challenge. When they transplanted regular interneurons, they saw no beneficial effects, presumably because Alzheimer's disease creates a toxic environment in the brain.
The scientists then genetically boosted the activity of inhibitory interneurons by adding a protein called Nav1.1. They discovered that the interneurons with enhanced function were able to overcome the toxic disease environment and restore brain function.
"These optimized neurons are like master conductors," said Palop. "Even with a declining orchestra, they can restore the rhythms and harmony needed for cognitive functions."
Conductors Engineered for Alzheimer's Disease
The findings could eventually lead to the development of new treatment options for patients with Alzheimer's disease.
"Besides the applications this cell engineering and transplantation approach may find in regenerative medicine, our findings support the broader concept that enhancing the function of interneurons can counteract key aspects of Alzheimer's disease," said Lennart Mucke, MD, director of the Gladstone Institute of Neurological Disease.
In addition to examining if the cell therapy could be translated from mice to humans, Palop and his team are working to identify potential drugs as an alternative way to enhance the function of inhibitory interneurons.
"Advancing our understanding of Alzheimer's disease and identifying potential new treatment strategies are critical to addressing the escalating global health crisis," said Elizabeth Edgerly, PhD, executive director of the Alzheimer's Association, Northern California and Northern Nevada chapter. "We were proud to support Dr. Palop's research and vision with an Investigator Initiated Research Grant award." The Alzheimer's Association, which funded part of the study, is the world's largest nonprofit funder of Alzheimer's research.
Source: Eurekalert
Palop's previous studies showed that, in mouse models of Alzheimer's, the inhibitory interneurons do not work properly. So, the rhythms that organize the excitatory cells are disturbed and fail to function harmoniously, causing an imbalance in brain networks. This, in turn, affects memory formation and can lead to epileptic activity, which is often observed in patients with Alzheimer's disease.
Healthy Mitochondria May Stop Alzheimer’s Disease
Enhancing mitochondrial proteostasis reduces the formation of amyloid plaques and delays amyloid-beta proteotoxic diseases, such as Alzheimer's disease.
Advertisement
His team found a way to reengineer inhibitory interneurons to improve their function. They showed that these enhanced interneurons, when transplanted into the abnormal brain of Alzheimer mice, can properly control the activity of excitatory cells and restore brain rhythms.
"We took advantage of the fact that transplanted interneurons can integrate remarkably well into new brain tissues, and that each interneuron can control thousands of excitatory neurons," said Palop, who is also an assistant professor of neurology at the University of California, San Francisco. "These properties make interneurons a promising therapeutic target for cognitive disorders associated with brain rhythm abnormalities and epileptic activity."
First, the scientists had to overcome a significant challenge. When they transplanted regular interneurons, they saw no beneficial effects, presumably because Alzheimer's disease creates a toxic environment in the brain.
The scientists then genetically boosted the activity of inhibitory interneurons by adding a protein called Nav1.1. They discovered that the interneurons with enhanced function were able to overcome the toxic disease environment and restore brain function.
"These optimized neurons are like master conductors," said Palop. "Even with a declining orchestra, they can restore the rhythms and harmony needed for cognitive functions."
Conductors Engineered for Alzheimer's Disease
The findings could eventually lead to the development of new treatment options for patients with Alzheimer's disease.
"Besides the applications this cell engineering and transplantation approach may find in regenerative medicine, our findings support the broader concept that enhancing the function of interneurons can counteract key aspects of Alzheimer's disease," said Lennart Mucke, MD, director of the Gladstone Institute of Neurological Disease.
In addition to examining if the cell therapy could be translated from mice to humans, Palop and his team are working to identify potential drugs as an alternative way to enhance the function of inhibitory interneurons.
"Advancing our understanding of Alzheimer's disease and identifying potential new treatment strategies are critical to addressing the escalating global health crisis," said Elizabeth Edgerly, PhD, executive director of the Alzheimer's Association, Northern California and Northern Nevada chapter. "We were proud to support Dr. Palop's research and vision with an Investigator Initiated Research Grant award." The Alzheimer's Association, which funded part of the study, is the world's largest nonprofit funder of Alzheimer's research.
Source: Eurekalert
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Polygenic testing of multiple gene variants can more accurately predict cognitively normal adults who may be at a higher risk of developing Alzheimer's disease
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 Lack of Insight of Memory Problems Linked to Alzheimer’s Disease PathologyNot being aware of memory problems predicts onset of Alzheimer's disease, revealed new study. | Advertisement
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