Showing posts with label Neuroscience. Show all posts
Showing posts with label Neuroscience. Show all posts

Monday, October 6, 2025

Dendritic Nanotubes Alzheimers Discovery 2025

Dendritic Nanotubes: New Brain Bridges Linked to Early Alzheimer's Clues

Edited by: Fasi Uddin

Neuronal nanotubes play a role in intercellular transport and disease. Credit: Science (2025), DOI: 10.1126/science.adr7403.

Snapshot

Scientists have identified a novel form of microscopic bridge in the braindendritic nanotubes (DNTs)that may help explain how Alzheimer's-related proteins spread between neurons. The discovery, reported in Science, combines advanced imaging, machine learning and computational modelling to suggest DNTs could be an early driver of amyloid-beta accumulation and neurodegeneration.

Neuronal communication and nanotube context

Neurons in the brain communicate through synapsestiny junctions that transmit electrical and chemical signals. In contrast, some non-neuronal cells exchange materials directly using microscopic nanotube bridges. Among these, tunnelling nanotubes (TNTs) are known to facilitate the transfer of substances between certain cell types. While TNTs have been observed in isolated brain neurons, their role and existence within fully developed brain tissue have remained uncertain.

Discovery of Dendritic Nanotubes (DNTs)

A team of researchers has discovered a new kind of nanotube that seems to function as a bridge, transferring materials between dendritesthe branching extensions of neurons. Reported in Science, the study introduces "dendritic nanotubes" (DNTs) and explores their potential link to the build-up of amyloid-beta (Aβ), a peptide associated with Alzheimer's disease.

Imaging and Confirmation

The scientists identified these actin-rich DNTs in both mouse and human brain tissue using advanced superresolution (dSRRF) and electron microscopy. The nanotubes were observed linking dendrites within the cortex and their identity was confirmed through specialized imaging combined with machine learning analysis.

Structural Uniqueness and Dynamics

According to the researchers, machine learning-based classification confirmed that the shape of these nanotubes was unlike any known synaptic structure. "In cultured neurons, we observed these nanotubes forming dynamically and identified a unique internal composition that clearly distinguishes them from other neuronal extensions," the authors explained.

Sealed Architecture and Transport

Unlike the well-documented tunnelling nanotubes (TNTs), these newly discovered dendritic nanotubes (DNTs) behaved quite differently. Their ends were sealed rather than open, preventing tunnelling activity. Despite this, the DNTs still managed to transfer essential materials such as calcium ions and small molecules between neurons.

Experimental Transfer of Amyloid-Beta

The researchers sought to determine whether these dendritic nanotubes (DNTs) could transport amyloid-beta, a protein linked to Alzheimer's disease. By introducing amyloid-beta into neurons within mouse brain slices, they observed that DNTs transferred the peptides to neighbouring cells. When nanotube formation was inhibited, the spread diminished significantly.

Computational Simulations and Timing

Computer simulations revealed that DNT density increased prior to amyloid plaque formation in Alzheimer's model mice, indicating a potential role in teh disease's early stages.

Modelling Links DNTs to Disease Progression

"We discovered that the nanotube network undergoes significant alterations early in Alzheimer's diseasewell before amyloid plaques, its defining feature, begin to form," the authors noted. "Our computational model suggests that excessive nanotube activity may hasten toxic amyloid build-up in certain neurons, linking these structural changes to disease progression."

Future Directions and Implications

Although many questions remain, future studies could uncover further roles these dendritic nanotubes play in healthy and diseased brains. The findings illuminate a potential mechanism by which Alzheimer's pathology spreads, pointing to promising paths for early therapeutic intervention.

Why This Discovery Matters

The discovery of DNTs bridges an important gap between cellular observations and disease dynamics. Scientists have long debated how misfolded proteins such as amyloid-beta traverse neural circuits to seed plaques in distant brain regions. An anatomical conduitpresent before overt plaque formationprovides a feasible route for early propagation, which could help explain the stealthy onset of Alzheimer's symptoms. For readers seeking broader context on neuroscience and imaging advances, see FSNews365.

Diagnostic and Therapeutic Potential

If DNTs prove to be consistent features of early Alzheimer's, they could enable earlier diagnosis through imaging biomarkers or fluid tests indicating altered intercellular transfer. Therapeutically, strategies that reduce excessive nanotube formation or block peptide passage may offer a window to slow progression before neurons are irreversibly lost. Such approaches would complement ongoing trials that target amyloid clearance and tau pathology. For reports and clinical context on Alzheimer's research and translational work, consult Human Health Issues.

Multidisciplinary Methods Power the Finding

The work highlights a growing trend in neuroscience: integrating high-resolution optical imaging, electron microscopy and machine-learning classification to detect and validate subtle brain structures. These methods reduce the risk that findings are imaging artefacts and allow automated recognition of shapes across large datasets. For related interdisciplinary coverage that connects imaging, climate and human health perspectives, see Earth Day Harsh Reality.

Open Questions and Next Steps

Researchers caution that these findings mark the start of a longer research pathway. Key priorities include validating DNT prevalence across brain areas and patient populations, performing live-cell imaging to capture transport dynamics in real time and determining whether interventions that tamper with DNTs alter cognitive decline in animal models. Importantly, scientists must distinguish between normal physiological roles for dendritic contacts and pathological overactivity linked to toxic spread.

Broader Implications for Neurodegenerative Disease

Beyond Alzheimer's, DNTs could be relevant to conditions where protein propagation is implicatedsuch as Parkinson's disease and certain frontotemporal dementias. If nanotube-like bridges facilitate spread more generally, then targeting intercellular conduits could represent a novel, cross-disease therapeutic approach. For public-health and translational perspectives, readers may explore Human Health Issues and interdisciplinary analyses at Earth Day Harsh Realty.

Translating Discovery into Clinical Action

Translational science will require replication of DNT observations in larger human cohorts, biomarker discovery and validation, safety testing of candidate inhibitors and ultimately carefully designed clinical trails. Funding agencies and interdisciplinary consortia will be crucial in moving this discovery from microscopy to medicine. For contextual science coverage and policy discussion, FSNews365 maintains updates on imaging, AI and translational research.

Ethical Considerations and Caution

Modulating intercellular structures in the brain carries risk: DNTs may also play roles in healthy neuronal communication and plasticity. Any therapy targeting these bridges must avoid disrupting normal brain function. Ethical review, staged preclinical testing and broad stakeholder engagement will be essential steps as the field progresses.

Conclusion

This study adds a new layer to our understanding of how pathological proteins might move through the brain. Dendritic nanotubes are a promising anatomical concept that could explain early protein spread, and they open avenues for diagnostics and interventions targeted at a stage when therapies are most likely to succeed. Continued collaboration across imaging, computational and clinical teams will be crucial to translate this discovery into patient-care gains.

Further Reading & Resources

Source

Original Science report (Journal).

FSNews365 - imaging and neuroscience coverage: https://fsnews365.blogspot.com

Earth Day Harsh Reality - Interdisciplinary science: https://earthdayharshreality.blogspot.com

Human Health Issues Updates - Alzheimer's and clinical research: https://human-health-issues.blogspot.com


Sunday, September 14, 2025

deepinminiscope real time mouse brain

Groundbreaking DeepInMiniscope Revolutionizes Real-Time Mouse Brain Imaging

The DeepInMiniMicroscope, developed by UC Davis electrical engineering professor Weijian Yang, merges advanced optical technology with machine learning to capture high-resolution, three-dimensional images within living tissue. Credit: Mario Rodriguez/UC Davis

Researchers from the University of California, Davis, have unveiled a groundbreaking compact microscope designed to enable high-resolution, noninvasive monitoring of mouse brain activity in real time. This breakthrough marks a significant step forward in neuroscience, promising to reshape how scientists study brain function and behaviour and opening the door to new treatments for brain disorders.

"Our aim is to develop technology that can image brain activity in freely moving, naturally behaving mice, thereby expanding the behavioural research paradigm," explained Weijian Yang, professor of electrical and computer engineering. "The goal is to build a device that enables real-time study of how brain activity influences behaviour and perception."

This pioneering imaging system, named DeepInMiniscope, was published in a Science Advances Study on 12 September 2025 and highlights major technological advances in brain imaging.

A Leap Forward in Neuroscience Imaging Technology

Overcoming Limitations of Traditional Microscopes

DeepInMiniscope builds upon Professor Yang's prior research, advancing the field of miniature imaging systems. Traditional imaging technologies struggled with imaging biological samples due to light scattering in living tissue, poor signal contrast and computational challenges in reconstructing 3D features across large volumes.

By incorporating over 100 miniature high-resolution lenslets in an innovative mask design, the DeepInMiniscope solves these issues. A sophisticated neural network processes the images from each lenslet, enabling seamless 3D reconstruction with remarkable speed and accuracy.

Neural Network Drive Deep Insights

The neural network merges several machine learning techniques to form an unrolled neural network architecture that performs high-speed, high-resolution image reconstruction from limited training data.

"Our algorithm strikes a balance between interpretability, efficiency, scalability and precision," explained Feng Tian, a postdoctoral researcher in Yang's lab and first author of the study. "It can robustly process large datasets at remarkable speed."

This innovation enables scientists to capture neuronal activity in real time as mice behave naturally, a milestone that could not only transform lab research but also pave the way for future innovations in brain disorder treatments.

Compact, Wearable and Lightweight Design: A Researcher's Dream

DeepInMiniscope's compact design is a game-changer. Weighing only 10 grams and measuring 3 square centimeters--roughly the size of a grape--this miniature microscope is optimized for live, mobile animals. Unlike bulky imaging devices, it is a slim circuit board with an image sensor, minimizing weight and maximizing comfort for the test subjects.

Vision for the Future

Weijian Yang's ultimate goal is even more ambitious: a cordless device measuring just 2 square centimeters, comparable to a small hat for a mouse. This would enable long-term, untethered studies of brain activity in freely moving mice under natural conditions.

"By allowing real-time observation of brain activity in freely behaving mice, this technology enhances our understanding of how the brain processes information and governs behaviour, while also aiding research into brain disorders and future treatments for humans," said Yang.

Explore more about how artificial intelligence is transforming biomedical research.

Implications for Human Brain Disorder Research

The DeepInMiniscope represents more than an engineering marvel--it could profoundly impact medical science. By enabling the study of neural circuits in motion, this technology opens up new possibilities for understanding diseases such as Alzheimer's Parkinson's epilepsy and mental health disorders.

"This device allows researchers to track neuronal activity patterns over time, giving critical insight into how these disorders develop and how therapeutic interventions can be fine-tuned," noted Feng Tian.

Learn about cutting-edge research linking genetics and neurological diseases.

Pioneering a Paradigm Shift in Behavioral Science

This development aligns with a broader effort to study behaviour under naturalistic conditions, addressing the limitations of traditional lab-based experiments.

An exciting parallel development is found in how quantum physics innovations are influencing material science and medical research, highlighting the convergence of multiple cutting-edge disciplines in pursuit of knowledge.

Researchers hope that future iterations of the DeepInMiniscope will allow deeper exploration of how brain activity influences behaviour and perception in more complex environments, moving from mice to larger models and eventually to human applications.

Global Collaborative Efforts and Open Science

The success of DeepInMiniscope was made possible by a collaborative effort involving multidisciplinary teams of engineers, neuroscientists and computational experts. Such global collaborations are increasingly essential in driving breakthroughs.

Read more about how interstellar research inspires scientific discoveries.

A Step Toward Noninvasive Brain Monitoring in Humans

While the DeepInMiniscope is designed for small animals, it symbolizes a critical step toward noninvasive, high-resolution brain monitoring technologies for humans. The prospect of future wearable brain scanners, capable of tracking neural activity in real time, is now much closer to reality.

These devices could be revolutionary for diagnosing and managing neurological disorders, especially in natural environments outside hospitals.

Future Research and Innovations

Professor Yang and his team are already planning the next steps: optimizing the device to be wireless and miniaturized further, ensuring ease of use and broader adoption by researchers globally.

This work complements related research into revolutionary artificial intelligence models uncovering life's genetic secrets.

Conclusion: A New Era in Neuroscience and Medicine

The DeepInMiniscope represents a landmark achievement in neuroscience, redefining the way researchers observe and understand brain function. By fusing advanced optical engineering, deep learning and innovative miniaturization techniques, this technology empowers scientists to study the brain's complexity in real time without invasive measures.

"Our vision is to empower the scientific community with tools that reveal the brain's mysteries, while advancing treatments for debilitating neurological conditions," said Weijian Yang.

Explore more about cutting-edge sustainability initiatives and technological breakthroughs.

Source

"Unlock the future of neuroscience--discover how cutting-edge brain imaging technology reveals real-time neural activity in freely moving subjects driving medical breakthroughs."

Human Health Issues - "Discover advancements in medical technology and neuroscience research, empowering breakthroughs in diagnosing and treating brain disorders at Human Health Issue."

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Thursday, September 4, 2025

ai computer vision seeme detects consciousness coma

AI Tool SeeMe Detects Hidden Consciousness in Coma Patients Days Before Doctors

Study framework and analytical pipeline for SeeMe. Credit: Communications Medicine (2025). DOI: 10.1038/s43856-025-01042-y

A Groundbreaking Advance in Brain Injury Diagnosis

A team of scientists at Stony Brook University has unveiled and artificial Intelligence (AI) tool named SeeMe, capable of detecting subtle signs of consciousness in comatose brain injury patients days before traditional clinical methods. The research, published in Communications Medicine, demonstrates how SeeMe leverages computer vision to track micro facial movements--movements that are invisible to the human eye--providing clinicians with an earlier and more accurate picture of patient responsiveness.

This finding has far-reaching implications for critical care, rehabilitation strategies, and ethical decision-making in intensive care unit.

The Challenge of Detecting Consciousness in Coma Patients

When patients suffer acute brain injuries, doctors and families are often faced with agonizing uncertainty. Standard diagnostic methods, such as the Glasgow Coma Scale (GCS) or the Coma Recovery Scale-Revised (CRS-R), rely on visible signs of responsiveness like eye-opening or limb movement. However, these responses may appear days or even weeks after the brain begins to regain awareness.

While advanced imaging technologies such as EEG (electroencephalography) and fMRI (functional magnetic resonance imaging) can reveal hidden consciousness, they are expensive, not universally available, and impractical for repeated bedside monitoring. As a result, subtle or covert signs of consciousness often go unnoticed in the early stages of recovery.

This gap inspired researchers to design a low-cost, portable AI-based tool that could pick up on signs invisible to even experienced neurologists.

How SeeMe Works: Computer Vision at the Bedside

The SeeMe system uses high-resolution facial mapping, tracking pore-level movements at a scale of just ~0.2 millimeters. Patients are given simple verbal instructions such as:

  • "Open your eyes."
  • "Smile."
  • "Stick out your tongue."

SeeMe identifies subtle, stimulus-driven movements ahead of blinded rater detection in ABI coma patients. Credit: Communications Medicine (2025). DOI: 10.1038/s43856-025-01042-y

The AI then analyses subtle movement vectors--tiny changes in muscle activity--that may indicate a conscious response. Importantly, the tool was designed not to replace doctors but to complement clinical observations by adding a layer of measurable, objective analysis.

Study Design and Participants

  • 37 coma patients aged 18-85 with severe brain injuries (GCS ≤ 8) were recruited at Stony Brook University Hospital.
  • 16 healthy controls were also included for baseline comparisons.
  • Video sessions were recorded after sedation pauses deemed medically safe.
  • Responses were measured against standard scales: GCS eye score and CRS-R auditory score.

Two blinded raters evaluated each trial independently, applying strict screening rules to rule out artefacts. Non-parametric statistical methods, including the Kruskal-Wallis test and chi-square analyses, confirmed the robustness of the results.

Key Findings: Earlier and More Accurate Detection

The results revealed that SeeMe consistently detected signs of consciousness earlier than clinical examinations.

Eye-Opening Advantage

  • SeeMe: Detected eye-opening at an average of 9.1 (± 5.5) days post-injury.

  • Clinicians: Detected at an average of 13.2 (± 11.4) days post-injury.

  • Result: A 4.1-day lead time, which can make a critical difference in decision-making.

SeeMe detected eye-opening in 85.7% of patients (30 out of 36) compared to 71.4% with clinical exams (25 out of 36).

Mouth Movements and Tongue Responses

  • For patients without obstructing endotracheal tubes, SeeMe detected mouth movements in 16 of 17 cases (94.1%).

  • In seven patients where both SeeMe and clinical testing were possible, SeeMe identified consistent mouth responses 8.3 days earlier on average.

Neural Network Analysis

The team also trained a deep neural network on SeeMe-positive cases:

  • 81% accuracy in detecting command-specific eye-opening.
  • 65% overall accuracy across tasks.
  • Lower performance tongue protrusion (37%) and smiling (47%), showing that eye-opening is the strongest and most reliable indicator of consciousness.

Why Early Detection Matters

Early recognition of covert consciousness could dramatically reshape treatment pathways and ethical decisions in intensive care.

Supporting Families in Critical Decisions

Families often face life-or-death choices about continuing life support. If tools like SeeMe confirm early signs of awareness, they may feel more confident in pursuing rehabilitations instead of withdrawing care.

Improving Rehabilitation Outcomes

Rehabilitation is most effective when started early. By spotting responsiveness days in advance, SeeMe can help clinicians initiate therapies sooner, maximizing the patient's chances of recovery.

Complementing Clinical Practice

The researchers stress that SeeMe is not a replacement for traditional exams. Instead, it serves as a quantitative and objective partner, reducing the risk of overlooking subtle but meaningful responses.

Expert Insights

Lead investigators highlight the transformative potential of SeeMe.

According to the study authors:

"Patients with acute brain injury may display low-amplitude, stimulus-driven facial movements before visible responses appear. SeeMe demonstrates that some covertly conscious individuals show motor activity overlooked by clinicians."

This reinforces the importance of not underestimating early signals of life that traditional methods may miss.

The Future of Ai in Neurology

The SeeMe project marks an early step in the integration of AI-powered tools into bedside neurological care. Future developments could extend its application into:

  • Continuous ICU monitoring systems that alert doctors when hidden responses appear.
  • AI-assisted rehabilitation programs, tailoring therapy to subtle improvements.
  • Communication interfaces for patients who are conscious but unable to move or speak.

By bridging the gap between human observation and machine precision, AI  transform how we understand consciousness itself.

Giving a Voice to the Silent

The discovery of SeeMe effectiveness provides new hope for patients, families and clinicians navigating the uncertainty of coma care. By detecting responses invisible to the naked eye, this AI tool not only shortens the timeline for recognition of consciousness but also opens doors to earlier intervention, improved outcomes and more compassionate decision-making.

As AI technologies continue to merge with medicine, SeeMe highlights the powerful role of innovation in answering one of healthcare's most difficult questions: is anyone still there?

Source

"Discover how AI is reshaping brain injury care--follow us for breakthroughs at the intersection of medicine, technology and human resilience."

  • Human Health Issues - "Find trusted insights on neurological health, recovery and medical innovations at Human Health Issues."
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Saturday, July 5, 2025

adult hippocampal neurogenesis study

Human Brains Keep Growing New Neurons to Age 78, Karolinska Study Finds

Graphic showing new neurons forming within the dentate gyrus of the human hippocampus across different ages, up to 78 years. Credit: Public Domain

Groundbreaking Study from Karolinska Institutet

A study from Sweden's Karolinska Institutet, published in Science, reveals that neuron formation in the hippocamus persists into late adulthood-offering critical insight into the enduring adaptability of the human brain.

Historical Insight into Neurogenesis Research

The Role of the Hippocampus in Brain Function

the hippocampus, a region of the brain central to learning, memory and emotional regulation, has long intrigued scientists.

The 2013 Landmark Study

In 2013, Jonas Frisén's group at Karolinska Institutet published a landmark study demonstrating that new neurons can form in the adult human hippocampus. They achieved this by measuring carbon-14 levels in DNA extracted from brain tissue, allowing them to estimate the age of the cells.

Determining the Cells of Origin

Nevertheless, the degree and importance of adult neurogenesis remain subjects of scientific debate. Conclusive evidence has yet to confirm whether neural progenitor cells-the precursors to new neurons-exist and divide in adult humans.

"We have now succeeded in identifying the cells of origin, confirming that neuron formation continues in the adult hippocampus," says Professor Jonas Frisén, who led the study at Karolinska Institutet's Department of Cell and Molecular Biology.

From Birth Through to the Age of 78

In their latest investigation, the team harnessed an array of advanced techniques to study brain tissue from donors aged between birth and 78, collected from international biobanks.

Techniques and Tools Used

Using single-nucleus RNA sequencing to profile gene activity within individual nuclei, alongside flow cytometry to assess cellular characteristics, they then applied machine-learning tools to chart every stage of neuronal development-from stem cells to dividing immature neurons.

Spatial Gene Mapping with RNAscope and Xenium

To pinpoint the cell's whereabouts, the researchers employed RNAscope and Xenium-two techniques that reveal spatial patterns of gene activity. Both confirmed that the newly generated cells reside within the dentate gyrus of the hippocampus, a region crucial for memory formation, learning and cognitive flexibility.

Prospects for Novel Therapies

Results indicate that the precursors to adult neurons in human are broadly comparable to those in mice, pigs and monkeys, albeit with some variation in gene expression. Additionally, individual differences were marked: some adults possessed numerous progenitor cells, others scarcely any.

"This provides a vital piece of the puzzle in understanding the working of the human brain and how it changes over a lifetime," explains Frisén. "Our findings may also inform the development of regenerative therapies aimed at promoting neurogenesis in psychiatric and neurodegenerative conditions."

Collaborative Effort and Institutional Involvement

The study was carried out in close collaboration with Ionut Dumitru, Marta Paterlini and fellow researchers at Karolinska Institutet, alongside colleagues from Chalmers University of Technology in Sweden.

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Friday, July 4, 2025

brain organoid platform mild blast TBI research

Brain Organoid Platform Aims to Decode Mild Blast Traumatic Brain Injury in Military personnel

Traumatic Brain Injury: A Persistent Challenge for Military personnel

Traumatic brain injuries have remained a persistent issue among military personnel, with the Department of Defence reporting close to 516.000 cases globally between 2000 and 2024.

Johns Hopkins Launches POSITRONIC to Study mbTBI

A research team from Johns Hopkins Applied Physics Laboratory (APL) in Laurel, Maryland, together with the Johns Hopkins Bloomberg School of Public Health, is developing a next-generation brain-organoid platform to tackle this challenge. Their studyPlatform to Optimally Study Injury and TRauma On Neural Integrity and Circuitry (POSITRONIC), published in Frontiers in Bioengineering and Biotechnologyoutlines the core principles of platforms designed for investigating low-level blast exposure.

Understanding Low-Level Blast Exposure

"The cumulative impact of low-level blast exposure remains poorly understood, largely due to our limited capacity to detect subtle effects on the human body—effects that may appear immediately but unfold gradually over time," said Katy Carneal, Assistant Programme Manager for Biological and Chemical Sciences at APL.

The Hidden Risk of Repeated Exposure

Low-level blasts produce pressure waves that travel through the skull and interact with brain tissue: repeated exposure can result in mild blast-induced traumatic brain injury (mbTBI). Military and low enforcement personnel may be exposed to over 100 such blasts during certain training exercises—and considerably more over the course of their careers.

Developing the POSITRONIC Prototype Platform

"Our aim is to create a prototype platform that will enable a deeper understanding of mbTBI caused by repeated low-level blasts, using advances in brain organoid technology and non-invasive optical imaging," said Eyal Bar-Kochba, Chief Scientist at APL's Research and Exploratory Development Department (REDD) and lead investigator for POSITRONIC. "We hope this work will contribute to the development of preventative strategies, as well as improved diagnostic and treatment approaches."

Future-Ready Technologies to Study Brain Trauma

Limitations of Traditional TBI Models

Researchers have traditionally employed in vivo models—studies conducted on live animals—and in vitro models, involving cultured cells in laboratory settings, to investigate traumatic brain injuries. Yet, applying these findings to human cases has proved difficult due to the limited relevance of such models to human biology.

Brain Organoids: A Transformative in Vitro Tool

Enter brain organoids—an emerging in vitro model based on human cells. One of their chief advantages lies in their capacity to replicate complex neural networks and cellular dynamics.

Johns Hopkins Team Leads the Charge

Neurotoxicologists Thomas Hartung and Lena Smirnova, of the Bloomberg School, were  instrumental in advancing organoid platforms for trauma research. The POSITRONIC team is leading efforts to apply these brain organoids in studying repeated low-level blast exposures.

Simulating Blasts with Precision

"This highlights the flexibility of organoids as a viable alternative to animal models, offering a platform for exploring yet another complex condition," said Smirnova, Assistant Professor at the Bloomberg School.

Cultivating and Testing Brain Organoids Under Blast Pressure

Once cultivated, the brain organoids is linked to a pressure-generation system that allows researchers to simulate repeated low-level blast exposure, mirroring the pressure commonly encountered by service personnel during training exercises.

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Tuesday, May 27, 2025

infrared contact lenses human night vision

Revolutionary Lenses Allow Humans to See in the Dark Without Opening Eyes

participant putting contacts in. Credit: Yuqian Ma, Yunuo Chen, Hang Zhao

A Breakthrough in Noninvasive Vision Enhancement

A team of neuroscientists and materials scientists has developed contact lenses that grant infrared sight in humans and mice by transmuting infrared into visible light. Unlike traditional night-vision googles, these lensesreported in Cellneed no external power and allow perception of several infrared bands. Their transparency permits simultaneous viewing of infrared and visible light, with superior IR vision when the eyes are closed.

"Our findings pave the way for wearable, noninvasive technologies that could grant humans enhanced vision," remarks Tian Xue, lead researchers and neuroscientist at the University of Science and Technology of China. "The material offers immediate possibilities—flickering infrared light, for instance, may serve to relay data in contexts such as security, rescue operations, encryption or anti-counterfeiting."

How the Infrared Contact Lenses Work

Nano-particles Convert Infrared to Visible Light

The contact lens employs nano-particles capable of absorbing infrared radiation and converting it into light within the visible spectrum (approximately 400 to 700 nanometers), perceivable by mammalian eyes. These particles are designed to detect near-infrared wavelengths, ranging from 800 to 1600 nanometers—just beyond the natural limits of human vision.

Earlier Research and Motivation

The researchers had earlier demonstrated that injecting these nano-particles into the retina could grant mice infrared vision, though their aim was to develop a less intrusive alternative.

Design and Testing of the Contact Lenses

Safe Integration with Soft Lens Polymers

The researchers fashioned the contact lenses by integrating the nano-particles with pliable, non-toxic polymers commonly found in conventional soft lenses. Upon confirming their safety, the lenses were tested on both humans and mice.

procedures for infrared contacts. Credit: Sheng Wang

Mice Behavioral Evidence of Infrared Vision

The researchers observed that mice fitted with contact lenses exhibited behaviors indicative of infrared vision. When offered a choice between a dark enclosure and one lit with infrared light, lens-wearing mice opted for the dark, unlike their untreated counterparts.

Physiological and Brain Activation Indicators

The mice exhibited physical indicators of infrared vision, with their pupils narrowing in response to infrared light. Imaging also showed activation in the brain's visual processing centers when exposed to such wavelengths.

Human Trials and Performance

Recognition of Infrared Signals

Human participants wearing the infrared contact lenses were able to correctly identify flickering Morse code-style signals and determine the source direction of the infrared light.

"It's perfectly straightforward-without the contact lenses, the subjects sees nothing. With them on, they can plainly observe the flickering of the infrared light," remarked Xue.

Closed-Eye Detection Advantage

"We discovered that subjects were better at detecting the flickering when their eyes were closed, as near-infrared light passes through the eyelids more efficiently than visible light, reducing interference."

Research team places infrared contacts in participant's eyes. Credit: Yuqian Ma, Yunuo Chen, Hang Zhao

Multiband and Colour-Coded Infrared Vision

Assigning Colours to Infrared Wavelengths

A further modification to the lenses enables wearers to distinguish among various bands of infrared light, with nanoparticles designed to assign distinct colours to each wavelengthsuch as blue for 980 nm, green for 808 nm and red for 1,532 nm.

Aid for Colour-Blind Users

Beyond enhancing perception of infrared details, the colour-coded nanoparticles may also be adapted to assist those with colour blindness in detecting wavelengths they typically cannot see.

"Through converting red wavelengths into green ones, this innovation could help blind users perceive previously invisible elements," says Xue.

Improving Visual Clarity and Signal Detection

Wearable Glasses for Sharper Infrared Imaging

Due to the contact lenses' limited capacity for fine detail—owing to their closeness to the retina causing scattered light—the researchers devised a wearable glass system using the same nanoparticles, offering sharper infrared perception.

Future Developments in Sensitivity

At present, the contact lenses can solely detect infrared light emitted by LED sources, though scientists are striving to enhance the nanoparticles' sensitivity to pick up weaker infrared signals.

"In time, through collaboration with materials scientists and optics specialists, we aim to develop a contact lens boasting finer resolution and improved sensitivity," said Xue.

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Wednesday, March 5, 2025

epigenetic echoes violence genetic impact

Epigenetic Echoes: How Violence Imprints Lasting Genetic Marks on Future Generations

The 1982 Hama Massacre and Its Lasting Impact

The study is structured to compare genomic epigenetic markers in relation to varying degrees of violence exposure. Credit: Connie Mulligan.

In 1982, the Syrian government laid siege to Hama, resulting in the deaths of tens of thousands during sectarian violence. Four decades later, the memory of this massacre fueled rebels' efforts to overthrow the Assad regime responsible for the brutal act.

Genetic Imprints of War: A Legacy Passed Down

Another enduring consequence of the attack lies within the genetic makeup of Syrian families. Grandchildren of women who were pregnant during the siegedespite never experiencing the violence firsthandcarry its imprint in their genomes.

Epigenetics and the Transmission of Trauma

Inherited through maternal lineage, this genetic signature provides the first human evidence of a phenomenon previously observed only in animals—the intergenerational transmission of stress at the molecular level.

"Recognizing that trauma and violence can impact future generations should foster greater empathy and encourage policymakers to prioritize addressing violence," said Connie Mulligan, Ph.D., Professor of Anthropology and the Genetics Institute at the University of Florida, and senior author of the study.

"This phenomenon may offer insight into the persistent intergenerational cycles of abuse, poverty, and trauma observed worldwide, including in the United States."

How Trauma Leaves a Molecular Mark

While our DNA remains uncharged by lived experiences, epigenetic processes enable its functional tuning. Stress and environmental stimuli can lead to chemical modifications that adjust gene activity, potentially aiding adaptation, though the extent of these effects remains unclear.

Investigating the Epigenetic Legacy in Syrian Families

The chemical indicators identified by Mulligan and her team were the key targets in their investigation of Syrian family genetics. Although lab-based research has shown that animals can inherit stress-induced epigenetic modifications, demonstrating this humans has remained elusive.

A Groundbreaking Study on Generational Trauma

Mulligan collaborated with:

  • Rana Dajani, Ph.D., a molecular biologist at Hashemite University in Jordan
  • Catherine Panter-Brick, Ph.D., an anthropologist at Yale University, to carry out this groundbreaking study.

The research focused on tracking three generations of Syrian immigrants in the country.

The study's results were published in the journal Scientific Reports.

Three Generations, Three Unique Experiences

Some families experienced the Hama attack before seeking refuge in Jordan, while others avoided Hama but endured the recent civil war against the Assad regime.

The researchers gathered samples from grandmothers and mothers who were pregnant during the two conflicts, along with their children. This approach allowed for the inclusion of individuals who had encountered violence at distinct developmental stages.

A Control Group for Comparison

A third group consisted of families who had settled in Jordan before 1980, thereby avoiding the prolonged violence in Syria. These early immigrants provided a vital control group for comparison with families affected by the civil war.

The Science Behind the Study

Dajani, herself the daughter of refugees, worked intimately with the refugee community in Jordan to build rapport and encourage study involvement. She eventually obtained cheek swabs from 138 participants across 48 families.

"These families are eager to share their stories and have their voices heard," Mulligan remarked. "I believe we collaborated with every eligible family for this study."

Analyzing DNA for Epigenetic Modifications

In Florida, Mulligan's lab analyzed DNA for epigenetic modifications, investigating potential correlations with the families' exposure to violence.

The Lasting Epigenetic Impact of Violence

Genetic Markers Found in Grandchildren of Hama Survivors

Among the grandchildren of Hama survivors, researchers identified 14 genomic regions that had undergone modifications in response to the vilence experienced by their grandmothers. These findings suggest that stress-induced epigenetic changes can be inherited across generations, similar to patterns observed in animals.

Epigenetics Signatures in Directly Affected Individuals

The research identified 21 epigenetic sites in individuals who had directly experienced violence in Syria. Additionally, the study found that those exposed to violence in utero exhibited signs of accelerated epigenetic aging, a biological process potentially linked to increased susceptibility to age-related diseases.

A Shared Epigenetic Response to Stress

The majority of these epigenetic modifications exhibited a consistent pattern following exposure to violence, indicating a shared epigenetic response to stress —one that may impact not only those directly affected but also their descendants.

Broader Implications: Beyond War and Refugees

"Our research is applicable beyond refugee experiences; it extends to various forms of violence, including domestic abuse, sexual assault, and gun violence in the U.S.," Mulligan emphasized. "This issue warrants further study and greater attention."

Epigenetics and Human Health Risks

The precise impact of these epigenetic modifications on individuals carrying them remains uncertain. However, some studies have suggested a correlation between stress-induced epigenetic alterations and conditions such as diabetes.

A well-known study on Dutch famine survivors from World War II suggested that their descendants exhibited epigenetic modification associated with a higher likelihood ob obesity. While many such changes may be inconsequential, some could potentially impact human health, Mulligan noted.

Resilience Amid Trauma: A Testament to Human Strength

As Mulligan and her colleagues meticulously investigated the enduring genetic imprint of war and trauma, they were equally moved by the resilience of the families they studied. According to Mulligan, their narrative extended far beyond mere survival.

A Story Beyond Survival

"Despite enduring immense violence, these families extraordinary resilience. They continue to build meaningful lies, raise children, and uphold traditions," Mulligan remarked. "Such perseverance may be a distinctly human trait."

Source

"How does violence leave a lasting mark on our DNA? Discover groundbreaking research on inherited trauma and epigenetic changes."

Read the full article to explore how stress and trauma impact genetic memory and many affect future generations.

Read now and uncover the science behind genetic memory!

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