Researchers found that formalin fixation does not significantly alter the polarimetric properties of brain tissue, making it suitable for training machine-learning models. The study suggests that formalin-fixed brain tissue specimens can provide high-quality data for rapid and accurate diagnostic imaging in surgery.
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Researchers at Temple University Health System found that carbonic anhydrase inhibitors reduce inflammation, restore cell function and prevent cognitive impairment in mice with amyloid buildup. CAIs also improved cerebrovascular health and enhanced amyloid-clearing capacity.
Researchers at Gladstone Institutes have made a groundbreaking discovery about how neurons consume and metabolize glucose, a process crucial for maintaining normal energy levels. The study found that neurons rely on glycolysis to break down glucose, and its disruption can lead to severe learning and memory problems in mice.
Researchers at UC Davis discovered how oligodendrocyte-lineage cells transfer cell material to neurons in the mouse brain, providing a new mechanism for understanding brain maturation and finding treatments for neurological conditions. This discovery opens new possibilities for treating neurodegenerative diseases like Alzheimer's and P...
Research suggests astrocytes integrate external sensory inputs with internal states to modify calcium signaling towards neurons. This process could be crucial for behavioral responses and memory formation.
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Researchers found that astrocyte cells directly impact motor learning by maintaining an optimal molecular balance. Astrocytes' ability to regulate neurotransmitter glutamate affects the smoothness of movement and refinement of technique.
UCSF researchers identified glioma's cellular source of recurrent disease, finding cells shift to mesenchymal, radiation-resistant phenotype in response to standard therapy. Paracrine signals from tumor microenvironment drive this transition through AP1 pathway, leading to therapy resistance and tumor recurrence.
In a study published in Nature Communications, researchers found that astrocytes take over the role of cleaning up dead microglia, which are normally responsible for this task. This process is crucial for maintaining optimal conditions in the nervous system and preventing accumulation of cellular debris.
Researchers from Xi'an Jiaotong-Liverpool University found that brain stimulation combined with a nose spray containing nanoparticles can improve recovery after ischemic stroke. The treatment increased cognitive and motor functions, and weighed more quickly than those treated with TMS alone.
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A novel stem cell-gene therapy has been shown to be safe in humans, with no serious side effects reported in the first trial. The treatment targets motor neurons that die in patients with amyotrophic lateral sclerosis (ALS), a fatal neurological disorder.
Researchers at Buck Institute discover that blood-brain barrier cells influence neuron function and can cause problems rather than just being protective. This finding opens up new avenues for therapies targeting neurodegenerative diseases like Alzheimer's and Parkinson's.
A study found that disruptions in brain sphingolipid metabolism lead to neuronal damage and neurodegeneration in animal models, revealing a new molecular perspective on Gaucher's disease. The research also shows that neuronal activity triggers the production of glucosylceramide, a key factor in the development of this disorder.
A new study suggests that supplementing a diet with Ascidiacea, also known as sea squirts, reverses some main signs of aging in animal models. The researchers found that plasmalogens, vital to body processes, decrease with age and contribute to neurodegenerative diseases like Alzheimer's and Parkinson's.
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Researchers discovered that fusing Müller glia with adult stem cells can differentiate into ganglion cells, a type of neuron essential for vision. This finding brings hope for recovering the retina's regenerative capacity in humans.
A study found that intact astrocyte networks are essential for neural homeostasis, synaptic plasticity, and spatial cognitive abilities in adult mice. Disrupting these networks impairs spatial learning and memory due to altered neuronal excitability and compromised synaptic transmission.
Researchers discovered that pain neuron-derived peptide Reg3gamma suppresses microglial IDO1, a key enzyme of the kynurenine pathway, and enhances brain ATP production. This discovery provides novel insights into understanding tolerance to endotoxic death.
Scientists identify a specialized zone in Muller glia cells called the citrullination bunker that sequesters damaged proteins, preserving vision. Chronic engagement of this process may lead to retinal degeneration, but inhibiting it could delay or prevent disease.
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Researchers at Tohoku University have discovered a stimulation paradigm that can induce epilepsy resistance in experimental animals. Repeated stimulation resulted in a dramatic decrease in seizure response to the stimulus, suggesting a potential therapeutic strategy for managing epilepsy.
A team of researchers at Fudan University has found that the protein NeuroD1 does not induce microglia-to-neuron conversion as previously thought. Instead, it causes microglial cell death. The study suggests that this finding may be due to experimental artifacts and highlights the need for stringent evidence in scientific research.
Researchers create Opto-vTrap, a reversible inhibition system that can temporarily trap vesicles from being released, allowing for controlled brain activity. The technique enables temporary removal of fear memory in live mice, with potential applications in epilepsy treatment, muscle spasm treatment, and skin tissue expansion technolog...
A new study reveals that glial cells in the heart play a critical role in regulating heart rate and rhythm, as well as driving its development in the embryo. The discovery suggests that glia may also be important in other organs.
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A team of researchers from the University of Münster has identified a second barrier in the fly brain, formed by glial cells that regulate molecule distribution. The discovery is essential for understanding nervous system functioning and may have implications for human neural health.
Researchers found that glial cells are activated by interferon gamma in response to pathogen invasion, releasing signals to attract immune cells to fight infection. In the absence of disease or injury, blocked activation led to tissue inflammation, highlighting their role in maintaining healthy intestinal tissue.
Researchers at Hebrew University developed a novel approach to mapping brain white matter fiber architecture using Nissl staining. The technique, called Nissl-ST, reveals the hidden patterns and organization of glial cells in white matter, opening new avenues for studying brain development, aging, and neurodegenerative diseases.
A study by Purdue University researchers has discovered a way to use gene therapy to turn glial brain cells into neurons, restoring visual function. This process is more efficient and less damaging than stem cell therapy, offering new hope for patients who have lost vision or motor skills after a stroke.
A Johns Hopkins Medicine research team has provided a definitive view of the biological process leading to necrotizing enterocolitis (NEC), a dangerous inflammatory disease that can destroy a premature infant's intestinal lining. The loss of enteric glia leads to intestinal dysmotility, which is a key factor in NEC's genesis.
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Researchers at the University of Basel have discovered two new types of glial cells in the brain that may play a crucial role in brain plasticity and repair. These cells can potentially be used to treat neurodegenerative diseases such as multiple sclerosis.
A recent study found that environmental enrichment leads to specific epigenetic changes in the mouse brain, activating a minority of genes involved in cognition and mental health. These changes may inform future research on therapies for mental health disorders.
Scientists at IRB Barcelona have found that Lafora bodies accumulating in glial cells, not just neurons, are responsible for the disease's progressive degeneration. This discovery could lead to new treatments and insights into other neurodegenerative diseases.
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Researchers at Indiana University School of Medicine have successfully reprogrammed NG2 glial cells into functional neurons, potentially leading to improved recovery after spinal cord injuries. This breakthrough discovery has the potential to be translated into a clinically relevant repair strategy.
Researchers at Tohoku University discovered that neuronal and glial circuits form a loosely coupled super-network within the brain. Activation of metabotropic glutamate receptors in neurons can be influenced by the state of glial cells, suggesting potential for artificial control to enhance memory function.
Researchers found that genetic pathways allowing fish to regrow neurons remain present in mammals, but are turned off, blocking regeneration and healing. The study may advance genetic therapies for blindness and other neurodegenerative diseases.
A team of researchers has identified networks of genes that regulate neuron regeneration in certain animals, such as zebrafish. This discovery may lead to the development of new treatments for neurodegenerative disorders, including blindness and Parkinson's disease.
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Researchers at Temple University Health System have identified a new mechanism for promoting neuron regeneration after spinal cord injury, involving the metabolic switch associated with glucose metabolism in glial cells. The study found that upregulating glycolysis in glial cells can stimulate axon growth and improve functional recovery.
Researchers at the University of Münster discovered glial cells' active role in controlling signal transduction speed and precision. The study found that glial cells form membrane processes between axons, preventing electrical coupling and ensuring accurate neuronal signaling.
Scientists identified a mutation in the ACOX1 gene as the cause of Mitchell disease, a rare neurodegenerative disorder. The discovery was made using a combination of human genetics and fruit fly studies, which revealed a previously unknown role for peroxisomes in glial cells.
Researchers discovered a new neurodegenerative disorder, Mitchell disease, caused by hyperactive ACOX1 enzyme. A study in fruit flies identified therapeutic strategies to reverse damages specific to each condition.
Enteric glial cells convert into tumor growth promoters when exposed to secretions from colon tumors, regulating important intestinal functions and interacting with cancer stem cells. The study identifies key molecules involved in this process and offers new potential targets for cancer therapies.
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In a breakthrough, Johns Hopkins Medicine researchers successfully transplanted protective brain cells into mice without the need for lifelong anti-rejection drugs. The innovative approach exploits the immune system's natural tendencies to accept transplanted cells as 'self', allowing them to thrive and protect brain tissue long-term.
Researchers have developed a new gene therapy that converts glial cells into neurons, improving motor function in mice and potentially treating stroke. The treatment uses the NeuroD1 gene and has been shown to increase neuronal density and reduce brain tissue loss in mouse models of stroke.
Researchers found that glial cells, which make up 80% of brain cells, contribute to seizures by releasing glutamate, a chemical that transmits signals between neurons. The study suggests that targeting glial cells may lead to new treatments for epilepsy.
Mutations of a gene implicated in long QT syndrome trigger seizures due to its direct effects on neurons and glia, independent from heart function. This discovery challenges the assumption that seizures are secondary outcomes of cardiovascular disease.
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A new study published in Cell Reports sheds light on the mechanisms used by neural stem cells to reactivate, with key findings indicating that STRIPAK molecules play a crucial role in enabling reactivation. The research holds promise for future therapies to replace lost brain cells and facilitate brain damage repair.
Researchers have identified a cellular mechanism that prevents retinal regeneration in mammals, but allows for regeneration in zebrafish. By manipulating this pathway, it may be possible to restore lost vision by activating the retina's regenerative capacity.
Researchers at MIT's Picower Institute found that excess calcium in glia cells causes them to hyper-activate a molecular pathway leading to seizures. They identified calcineurin and sandman proteins as key players in the process, suggesting a promising avenue for future drug development.
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Researchers at the Buck Institute have identified a novel molecular mechanism that orchestrates harmful inflammatory signaling in glial cells, contributing to Parkinson's disease pathology. Blocking Furin 1, a catalytic protein, in dopaminergic neurons reduces toxic cross-talk and protects neurons from degeneration.
Researchers at Kanazawa University found that a neuroscience-protein regulates brain boundary formation in fly brains by exchanging with its partners between neurons and glial cells. The protein's balance of attraction and repulsion regulates boundary formation.
A new study has discovered a mechanism for regulating sleep in fruit flies that involves glial cells and an ingredient commonly found in energy drinks like Red Bull. The researchers found that the gene Eaat2 promotes wakefulness by limiting the length and intensity of sleep periods.
A new gene therapy can reprogram brain glial cells into functioning neurons, potentially treating stroke and neurodegenerative diseases. Researchers hope the innovative technology may one day help patients with severe neurological disorders.
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Researchers accidentally convert mature inhibitory neurons into dopamine-producing cells using a cocktail of proteins. The new cells show rhythmic activity and network connections similar to native dopaminergic neurons.
Researchers at UT Southwestern Medical Center discovered that mature inhibitory neurons can be transformed into a different type of neuron without relying on stem cells. The study reveals the possibility of changing mature neurons in adulthood and may lead to therapeutic strategies for treating neurological diseases.
Researchers have reversed congenital blindness in mice by changing supportive cells in the retina called Müller glia into rod photoreceptors. The new technique integrates Müller glia-derived rods into the brain's visual pathway, enabling mice to regain functional vision.
New study reveals that protein molecules in brain cells are broken down and replaced at different rates, depending on their location. The study found that proteins near the surface of the cell have shorter lifespans, while those involved in energy metabolism have longer lifespans.
Researchers at Michigan State University discovered a link between intestinal inflammation, irritable bowel syndrome, and communication between sensory neurons and enteric glia. The study found that specific molecular changes spark discomfort before symptoms appear.
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A study by McGill University Health Centre researchers has uncovered the mechanisms of overhydration leading to hyponatremia, a common condition in patients with traumatic brain injuries. The study reveals that glial cells detect overhydration and trigger the release of taurine, which inhibits hydration sensing neurons.
A study led by researchers at Linköping University found that amyloid beta, a protein linked to Alzheimer's disease, has different properties in different cell types. Glial cells can produce mature, less harmful forms of the protein, while neurons are more susceptible to damage.
A study published in the Journal of Neuroscience found that Müller glia play a crucial role in preserving retinal synapses and preventing vision loss in macular degeneration. The research suggests that Müller glia are an important therapeutic target for treating degenerative eye diseases.
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Researchers discovered that glial cells increase the acidity of the extracellular environment when exposed to ATP, leading to a massive release of acid. This triggers a feedback loop that prevents over-excitability of neurons by inhibiting neurotransmitter release.
Researchers uncover new insights into how stem cells transform into brain cells controlling leg movements in fruit flies, with implications for understanding comparable systems in humans. The study finds that two critical cell types, born from the same stem cell, facilitate the construction of a mature motor system.
Researchers discovered that impairing the partnership between brain cells leads to neurodegeneration. Apolipoprotein APOE4 was found to mediate lipid droplet accumulation, increasing oxidative stress and breaking protective mechanisms. This study provides new insights into Alzheimer's disease.
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