Articles tagged with Axons
A new study reveals that specific neural circuits can be activated to reverse structural abnormalities associated with autism spectrum disorder. Researchers successfully restored the axon initial segment's length and improved behavioral abnormalities in an ASD mouse model.
A new study at Florida Atlantic University maps the neural wiring system linked to a fly's split-second escape behaviors, revealing a decentralized communication strategy. The findings provide insight into how brains process information at extraordinary speed and may represent a conserved blueprint shared across species.
Scientists found that tumor-promoting fibroblasts attract nerve fibers through a vicious cycle of signaling and neurotransmitter release. This cycle promotes pre-cancerous growth and pulls in more nerve fibers, leading to a self-reinforcing loop. Disrupting this cycle may lead to new therapies for pancreatic cancer.
Scientists have identified two compounds, K102 and K110, that could promote remyelination and modulate immune function in multiple sclerosis. These compounds showed promising results in mouse models and human cells, suggesting potential for treating MS and possibly other neurological diseases.
A study by UC Riverside researchers identifies a strong connection between demyelination and seizure activity in multiple sclerosis. The findings suggest targeted treatments could address the root cause of seizures without suppressing overall brain activity.
Researchers found that ATP regulates protein condensation and cytoplasm viscosity, preventing harmful protein aggregates. Boosting ATP production decreases viscosity, dispersing existing and preventing future protein aggregations.
Scientists investigate whether living neurons can transport light through their axons, which would significantly change current models of the nervous system. If successful, it could have major implications for treating brain diseases and healing the brain.
Researchers at Johannes Gutenberg University Mainz have discovered that histone deacetylase 8 (HDCA8) inhibits the conversion of Schwann cells into their repair phenotype, slowing down peripheral nervous system recovery. Removing HDAC8 accelerates regeneration and restores sensory function.
Macrophages may help prevent peripheral neuropathy by slowing its onset and reducing damage. Researchers discovered that these immune cells produce chemokines to recruit other macrophages, which protect against sensory axon loss.
The study reveals that directional connections propagate signals in a downstream flow, leading to more complex activity patterns. Mathematical models also suggest that modularity and connectivity interact to foster dynamical complexity.
A recent SFU study reveals how indirect brain damage affects thalamus function after a stroke, potentially leading to new treatments. Researchers found that the amount of damage to the thalamus correlates with the level of impairment in patients.
Researchers propose a new model for understanding how information is transmitted in the brain by describing a unique axon morphology that changes size and modulates action potential speed
A new study reveals that the arm-like structures of mammalian brain cells, known as axons, are actually pear-shaped and not cylindrical tubes. The research team used high-pressure freezing electron microscopy to visualize the axons' structure, showing that they have a bubbly, pearl-like shape.
Researchers at UCLA discovered that protein netrin1 limits BMP signaling to specific regions of the spinal cord, crucial for sensory neuron development. This finding reshapes our understanding of complex spinal circuits and could inform future therapeutic strategies for spinal cord repair.
A team of researchers discovered a class of materials that mimic the behavior of axons by spontaneously amplifying electrical pulses. These materials can harness internal instabilities to create spiking behavior and amplify signals, potentially leading to more efficient computing and artificial intelligence.
Researchers have developed a new therapy called PIPE-307 that targets an elusive receptor on certain cells in the brain, prompting them to mature into myelin-producing oligodendrocytes. This could potentially reverse damage caused by multiple sclerosis, leading to improved movement, balance, and vision.
Researchers from Jilin University provide a comprehensive overview of brain injury biomarkers, including neuron-specific enolase, ubiquitin C-terminal hydrolase-L1, and neurofilament proteins. These biomarkers can help identify brain injuries and predict disease progression.
Scientists at Kyushu University created QDyeFinder, an AI pipeline that untangles the dense neuronal networks in the brain. The system uses a super-multicolor labeling protocol to tag neurons and then automatically identifies their structure by matching similar color combinations.
A recent study discovered a critical brain signal mediated by dopamine and its 'D2' receptors that plays a crucial role in timing actions. The research team used novel imaging techniques to observe this activity before self-timed presses, finding a gradual increase in brain signals about half a second prior.
Research finds that female brains have narrower and less dense axons, making them more prone to damage from concussion. This leads to more severe cognitive deficits in females compared to males after a head injury.
A team of Harvard researchers, led by Jeff Lichtman, has created the largest synaptic-resolution, 3D reconstruction of a piece of human brain to date. The dataset contains 1,400 terabytes of data on neural connections in a tiny piece of human temporal cortex.
Depletion of axonal mitochondria disrupts autophagy, leading to abnormal protein build-up in neurons. Restoring mitochondrial levels restores autophagy and recovers impaired neuron function.
Researchers at University of Cologne discover Cnicin, a plant-based compound that significantly accelerates axon growth in animal models and human cells. This breakthrough has the potential to treat paralysis and neuropathy by enabling nerves to regenerate more quickly.
Researchers at The University of Tokyo successfully connected lab-grown brain-mimicking tissue using axonal bundles, mimicking natural brain connections. This breakthrough enables the study of complex brain networks and their role in various neurological and psychiatric conditions.
Researchers discovered that mature oligodendrocytes, critical for brain function, can survive for up to 45 days after a fatal trauma, defying the classical programmed cell-death pathway. This finding opens new avenues for understanding and potentially preventing damage caused by aging and neurodegenerative diseases.
The study reveals that two neural pathways in the paraventricular nucleus of the thalamus participate in dynamic regulation of goal pursuits, with PVT+ neurons encoding execution and termination of actions, respectively. Activity in these neurons mirrors motivation parameters such as vigor and satiety.
A recent study by researchers at LMU Munich discovered that neural networks adapt to sensory stimulation on an individual nerve fiber basis, rather than transferring improvements to neighboring fibers. This finding suggests that varied sensory experience throughout life is essential for maintaining cognitive fitness.
Indiana University researchers have found that nicotinamide nucleotide adenylyl transferase 2 (NMNAT2) plays a critical role in protecting the brain from aging and neurodegenerative diseases. The enzyme provides energy to axons, enabling them to carry out nerve impulses and maintain healthy function.
A team of neuroscientists has discovered that oligodendrocytes, myelin-forming cells, accelerate glucose consumption to deliver energy-rich molecules to rapidly firing axons. This communication is mediated by potassium signals and maintains axonal health.
Researchers found an inverse relationship between axon loss and demyelination, suggesting that 'bad' myelin can be more damaging than its absence. This study identifies potential therapeutic targets for diseases associated with myelin defects and inflammation in the nervous system.
A single neuron in C. elegans worm uses multiple neurotransmitters to control egg-laying and locomotion, demonstrating the ability to 'borrow' serotonin from other neurons. The study reveals how a single neuron can influence complex behaviors over multiple timescales.
Researchers at CityU and HKUMed developed genetically modified human neural stem cells that promote neural circuit reconstruction, reduce glial scar accumulation, and enhance axon outgrowth. The therapy demonstrates potential for treating severe spinal cord injuries with functional recovery.
A Monash University study using roundworms found that certain foods, such as apples and herbs, can help protect against brain function deterioration. The researchers discovered that a molecule present in these foods, ursolic acid, causes a gene to turn on, making a specific type of fat that prevents axon fragility.
A study published in Science reveals that ganglia in the neck region are responsible for disrupting melatonin production and causing sleep disturbances in people with heart conditions. Researchers found that macrophages accumulate in the ganglion, leading to inflammation and scarring, which can be treated with drugs.
Researchers found that Perlecan deficiency causes axonal segments to break apart during development, leading to synaptic connection loss. The protein's critical role depends on its secretion from multiple cell types, not just neurons.
A team of neurobiologists has found that fruit flies possess glial sheath structures similar to those in vertebrates, enabling rapid transmission of nerve impulses. The study reveals the evolution of these structures and their role in supporting neuronal function.
A team of researchers found that a small population of nerve cells exists in everyone that could be coaxed to regrow, potentially restoring sight and movement. The discovery provides new insights into how axons grow and could lead to effective therapies for blindness, paralysis, and other disorders caused by nerve damage.
A study explores the role of dynamin protein DYN-1 in axonal fusion, revealing its ability to guide injury-induced reparative responses. Researchers found that DYN-1 regulates levels of fusogen, a transmembrane glycoprotein essential for physical repair of damaged axons.
The study reveals that gasdermin E drives changes in neurons that contribute to disease progression, leading to mitochondrial damage and axon degeneration. Inactivating gasdermin E prevents cellular damage and delays the progression of ALS in mice.
Researchers at DZNE discovered that centrosome controls neuronal migration but not axon growth. The study used novel molecular tools to show that centrosomal activity influences radial migration of projection neurons.
In a breakthrough study, researchers at Münster University revealed that mechanical tearing is the primary mechanism behind neurite pruning in sensory nerve cells of fruit flies. This process, which occurs during development, involves strong body contractions causing stress on fragile neurites, leading to their severance and removal.
A research team led by Dr. Eddie Ma Chi-him identified a therapeutic small molecule M1 that increases mitochondrial dynamics and sustains long-distance axon regeneration, restoring visual functions in mice. Regenerated axons elicited neural activities and survived for four weeks after optic nerve injury.
A new hallmark of ALS has been identified, revealing that loss of the RNA processing protein SFPQ leads to motor neuron degeneration. Defective mRNAs accumulate in axons and interfere with normal function, pointing to a possible new target for therapy.
Scientists at King's College London and the University of Bath have made a groundbreaking discovery about a molecule that plays a crucial role in nerve cell development. The study found that this molecule, known as SNRNP70, is not only present in the nucleus but also in the cytoplasm of nerve cells, where it shapes messenger RNA strand...
Researchers found that propofol decreases intracellular transport of proteins in neurons, impacting vesicle movement and axonal delivery. This study contributes to understanding how propofol causes anesthesia and may lead to the development of better anesthetic drugs.
Researchers found that blocking SARM1 prevents axon loss in neurodegenerative diseases, including Parkinson's and ALS. The study suggests new therapeutic approaches for diseases defined by axon loss, with potential treatments involving small molecule inhibitors or gene therapy.
Researchers created a 3D electrode array that maps the locations and activity of up to 1 million potential synaptic links in living brains. The system uses recordings of millisecond-scale evolution of electrical pulses in tens of thousands of neurons, allowing for dense and accurate mapping of brain circuits.
A University at Buffalo-led study suggests the huntingtin protein is involved in neuronal injury and regeneration. The research found that HTT moves from the injury site to the cell body, carrying components necessary for survival.
Researchers at HHMI's Janelia Research Campus have discovered a new type of synapse between neurons and their primary cilia, which allows for long-term changes in the cell's chromatin. This discovery could help scientists better understand how cells communicate and may lead to the development of more selective medications.
Researchers at CSIC-UMH have identified dozens of new regulatory proteins involved in guiding neural axons to their targets, a key process during nervous system development. These findings provide new avenues for understanding brain function and congenital defects.
A new GPU-based machine learning algorithm, ReAL-LiFE, can rapidly analyze large amounts of data from diffusion Magnetic Resonance Imaging (dMRI) scans of the human brain. This allows for faster analysis and prediction of brain connectivity, enabling better understanding of brain-behaviour relationships at scale.
Daily gabapentin treatment restored fine motor functions in mice's upper extremities and continued to show functional improvements even after treatment was stopped. The drug blocks the activity of a protein that hinders re-growth of axons, enabling post-stroke central nervous system repair to progress in a coordinated way.
Research on experimental drug NU-9 invents by Northwestern University scientists reveals it is more effective than existing FDA-approved drugs for ALS treatment. NU-9 also repairs the axons of diseased upper motor neurons in ALS mouse model, offering a potential new approach to treating the devastating disease.
A study published in PLOS Biology found that despite the functional importance of connections between far-reaching brain regions, the actual number of these connections is low. Researchers estimated 2.5 billion long-range axons in the cerebral cortex, but found that only a small percentage directly connected key functional areas.
Researchers observed that chandelier cells, which regulate cortical circuit activity, communicate with other neurons shortly after birth, influencing brain development. This interaction is crucial for normal brain function and may be disrupted in neurological disorders.
Researchers have discovered that sigma 1 receptor plays a crucial role in protecting retinal ganglion cells from damage in glaucoma. The protein enables astrocytes to secrete supportive factors for neurons, improving their survival and function.
Researchers found that myelination, even patchy on interneurons, is required for full inhibitory potential. Myelin loss can cause abnormal brain activity and lead to cognitive impairments.
Researchers at the University of Illinois Chicago found a promising treatment for neurodegenerative diseases by stopping nerve cell degeneration. A peptide has been identified that inhibits mitochondrial fission and lets nerve cells grow normally.
Researchers found increased myelination in areas associated with emotions and memory in individuals with anxiety and PTSD, correlating with specific symptoms. This study provides a possible explanation for individual variation in stress response and may lead to targeted treatments.
Researchers find that toxic aggregates form inside brain cells, causing axon damage and neuronal death. Silencing specific proteins can block the aggregation process, potentially preventing or treating prion diseases and other neurodegenerative disorders.