Friday, 29 June 2018

Researchers Discover Key Link Between Mitochondria and Cocaine Addiction


Researchers Discover Key Link Between Mitochondria and Cocaine Addiction
For years, scientists have known that mitochondria—the power source of cells—play a role in brain disorders such as depression, bipolar disorder, anxiety and stress responses. But recently scientists at the University of Maryland School of Medicine (UMSOM) have identified significant mitochondrial changes in brain cells that take place in cocaine addiction, and they have been able to block them.

In mice exposed repeatedly to cocaine, UMSOM researchers were able to identify an increase in a molecule that plays a role in mitochondria division (or fission) in a reward region of the brain. Researchers were able to block this change by using a special chemical, Mdivi-1. The researchers also blocked responses to cocaine by genetically manipulating the fission molecule within the mitochondria of brain cells, according to research published in Neuron.

“We are actually showing a new role for mitochondria in cocaine-induced behavior, and it’s important for us to further investigate that role,” said Mary Kay Lobo, PhD, Associate Professor of Anatomy and Neurobiology.

The researchers initially studied the mitochondria in cocaine-exposed mice and determined that mitochondria fission increased in the major reward region of the brain. To confirm this same change in humans, researchers were able to identify similar changes in the mitochondrial fission molecule in tissue collected from post mortem individuals who were cocaine dependents.

Dr. Lobo said that this latest research could help UMSOM researchers better understand changes in brain cells and mitochondria from other addictive disorders. “We are interested to see if there are mitochondrial changes when animals are taking opiates. That is definitely a future direction for the lab,” she said.

Journal article:
https://www.cell.com/neuron/abstract/S0896-6273(17)31090-5

Source:
http://www.medschool.umaryland.edu/news/2018/University-of-Maryland-School-of-Medicine-Researchers-Discover-Key-Link-Between-Mitochondria-and-Cocaine-Addiction.html

#mitochondria #cocaineaddiction #nucleusaccumbens #drp1 #Mdivi-1 #neuroscience

Tuesday, 26 June 2018

Alzheimer’s drug turns back clock in powerhouse of cell


Alzheimer’s drug turns back clock in powerhouse of cell
The experimental drug J147 is something of a modern elixir of life; it’s been shown to treat Alzheimer’s disease and reverse aging in mice and is almost ready for clinical trials in humans. Now, Salk scientists have solved the puzzle of what, exactly, J147 does. In a paper published January 7, 2018, in the journal Aging Cell, they report that the drug binds to a protein found in mitochondria, the energy-generating powerhouses of cells. In turn, they showed, it makes aging cells, mice and flies appear more youthful.

“This really glues together everything we know about J147 in terms of the link between aging and Alzheimer’s,” says Dave Schubert, head of Salk’s Cellular Neurobiology Laboratory and the senior author on the new paper. “Finding the target of J147 was also absolutely critical in terms of moving forward with clinical trials.”

Schubert’s group developed J147 in 2011, after screening for compounds from plants with an ability to reverse the cellular and molecular signs of aging in the brain. J147 is a modified version of a molecule (curcumin) found in the curry spice turmeric. In the years since, the researchers have shown that the compound reverses memory deficits, potentiates the production of new brain cells, and slows or reverses Alzheimer’s progression in mice. However, they didn’t know how J147 worked at the molecular level.

In the new work, led by Schubert and Salk Research Associate Josh Goldberg, the team used several approaches to home in on what J147 is doing. They identified the molecular target of J147 as a mitochondrial protein called ATP synthase that helps generate ATP—the cell’s energy currency—within mitochondria. They showed that by manipulating its activity, they could protect neuronal cells from multiple toxicities associated with the aging brain. Moreover, ATP synthase has already been shown to control aging in C. elegans worms and flies.

“We know that age is the single greatest contributing factor to Alzheimer’s, so it is not surprising that we found a drug target that’s also been implicated in aging,” says Goldberg, the paper’s first author.

Further experiments revealed that modulating activity of ATP synthase with J147 changes the levels of a number of other molecules—including levels of ATP itself—and leads to healthier, more stable mitochondria throughout aging and in disease.

“I was very surprised when we started doing experiments with how big of an effect we saw,” says Schubert. “We can give this to old mice and it really elicits profound changes to make these mice look younger at a cellular and molecular level.”

The results, the researchers say, are not only encouraging for moving the drug forward as an Alzheimer’s treatment, but also suggest that J147 may be useful in other age-associated diseases as well.

“People have always thought that you need separate drugs for Alzheimer’s, Parkinson’s and stroke” says Schubert. “But it may be that by targeting aging we can treat or slow down many pathological conditions that are old-age-associated.”

The team is already performing additional studies on the molecules that are altered by J147’s effect on the mitochondrial ATP synthase—which could themselves be new drug targets. J147 has completed the FDA-required toxicology testing in animals, and funds are being sought to initiate phase 1 clinical trials in humans.

Journal article:
https://onlinelibrary.wiley.com/doi/full/10.1111/acel.12715

Source:
https://www.salk.edu/news-release/alzheimers-drug-turns-back-clock-powerhouse-cell/

#alzheimersdisease #mitochondria #J147 #aging #neuroscience

Highlights of the Summer Sky


Highlights of the Summer Sky
What can you see in the night sky this summer? The featured graphic gives a few highlights for Earth's northern hemisphere. Viewed as a clock face centered at the bottom, early (northern) summer sky events fan out toward the left, while late summer events are projected toward the right. Objects relatively close to Earth are illustrated, in general, as nearer to the cartoon figure with the telescope at the bottom center -- although almost everything pictured can be seen without a telescope.

As happens during any season, constellations appear the same year to year, and meteor showers occur on or near the same dates. For example, like last year, the stars of the Summer Triangle will be nighttime icons for most the season, while the Perseids meteor shower will peak in mid-August, as usual.

Highlights specific to this summer's sky include that Jupiter will be visible after sunset during June, and Venus will shine brightly in the evening sky during July and August. Saturn and Mars should be visible during much of this season's night, with Saturn appearing in the direction opposite the Sun in late June, and Mars at opposition in late July. Finally, a total lunar eclipse should be visible to anyone who can see the Moon in late July.

Image & info via APOD
https://apod.nasa.gov/apod/astropix.html
Illustration Credit & Copyright: Universe2go.com

#universe #space #NASA #science

Wednesday, 20 June 2018

Evolving Prominence


Evolving Prominence
A small prominence hovered above the sun's surface over a two-day period (June 12-14, 2018) before breaking off into space. Prominences are cooler, darker clouds of plasma tethered above the sun by magnetic forces. These clouds of gases are notoriously unstable. The images were taken in the 304 Angstrom wavelength of extreme ultraviolet light.

Credit: Solar Dynamics Observatory, NASA.
https://sdo.gsfc.nasa.gov/gallery/potw/item/910

#sun #universe #space #science #prominences

Northern Lights and Noctilucent Clouds


Northern Lights and Noctilucent Clouds
Skies after the near-solstice sunset on June 17 are reflected in this calm lake. The tranquil twilight scene was captured near Bashaw, Alberta, Canada, northern planet Earth. Usually spotted at high latitudes in summer months, night shining or noctilucent clouds hang just above the horizon, transfusing light into a darker sky.

Near the edge of space, the icy apparitions are condensations on meteoric dust or volcanic ash still in sunlight at extreme altitudes. Also near the edge of space on this short northern night, solar activity triggered the lovely apparition of aurora borealis or northern lights.

What are noctilucent clouds?
Noctilucent clouds are also called Polar Mesospheric Clouds, PMCs. They are 80-85 km high (50-53 mile) a few km below the mesopause, the coldest part of the atmosphere.
NLCs are comprised of extremely small ice crystals some 0.1 micron (1/10,000 mm) diameter.

We see them by sunlight scattered by the crystals which are not large enough to show iridescent effects. Their bluish coloration is likely a result of absorption of red light by the stratospheric ozone layer. Occasionally they show reds and golds from the colour of low sunlight illuminating them.

NLC formation requires a combination of very low temperatures, a source of water vapour, and nuclei on which ice can grow.

Image & info via APOD
https://apod.nasa.gov/apod/astropix.html
Image Credit & Copyright: Adrien Mauduit
https://www.adphotography-online.com/

#naturalphenomena #noctilucentclouds #NASA #science

Tuesday, 19 June 2018

Stuttering: Stop signals in the brain prevent fluent speech


Stuttering: Stop signals in the brain prevent fluent speech
One per cent of adults and five per cent of children are unable to achieve what most of us take for granted—speaking fluently. Instead, they struggle with words, often repeating the beginning of a word, for example “G-g-g-g-g-ood morning” or get stuck with single sounds, such as “Ja” for “January” although they know exactly what they want to say.

What processes in the brain cause people to stutter? Previous studies showed imbalanced activity of the two brain hemispheres in people who stutter compared to fluent speakers: A region in the left frontal brain is hypoactive, whereas the corresponding region in the right hemisphere is hyperactive. However, the cause of this imbalance is unclear. Does the less active left hemisphere reflect a dysfunction and causes the right side to compensate for this failure? Or is it the other way around and the hyperactive right hemisphere suppresses activity in the left hemisphere and is therefore the real cause of stuttering?

Scientists at the Max Planck Institute for Human Cognitive and Brain Sciences (MPI CBS) in Leipzig and at the University Medical Center Göttingen have now gained crucial insights: The hyperactivity in regions of the right hemisphere seems to be central for stuttering: “Parts of the right inferior frontal gyrus (IFG) are particularly active when we stop actions, such as hand or speech movements”, says Nicole Neef, neuroscientist at MPI CBS and first author of the new study. “If this region is overactive, it hinders other brain areas that are involved in the initiation and termination of movements. In people who stutter, the brain regions that are responsible for speech movements are particularly affected.”


Two of these areas are the left inferior frontal gyrus (IFG), which processes the planning of speech movements, and the left motor cortex, which controls the actual speech movements. “If these two processes are sporadically inhibited, the affected person is unable to speak fluently”, explains Neef.

The scientists investigated these relations using Magnetic Resonance Imaging (MRI) in adults who have stuttered since childhood. In the study, the participants imagined themselves saying the names of the months. They used this method of imaginary speaking to ensure that real speech movements did not interfere with the sensitive MRI signals. The neuroscientists were then able to analyse the brain by scanning for modified fibre tracts in the overactive right hemisphere regions in participants who stutter.

Indeed, they found a fibre tract in the hyperactive right network that was much stronger in affected persons than in those without speech disorders. “The stronger the frontal aslant tract (FAT), the more severe the stuttering. From previous studies we know that this fiber tract plays a crucial role in fine-tuning signals that inhibit movements”, the neuroscientist states. “The hyperactivity in this network and its stronger connections could suggest that one cause of stuttering lies in the neural inhibition of speech movements.”

Source:
http://www.cbs.mpg.de/stuttering-in-the-brain

Journal article:
https://academic.oup.com/brain/article/141/1/191/4710058

Image:
Typically, the right IFG stops the flow of speech, whereas the left one supports it. In people who stutter, these two areas are conversely activated: The right IFG is overactive and shows tightened connections with the frontal aslant tract (FAT), which is a sign of a strengthened movement inhibition. This interrupts the flow of speech and might inhibit activity in the left IFG.
© MPI CBS

#stuttering #speech #neuroimaging #frontalaslanttract #motorcortex #neuroscience

Direct amygdala stimulation can enhance human memory


Direct amygdala stimulation can enhance human memory
Direct electrical stimulation of the human amygdala, a region of the brain known to regulate memory and emotional behaviors, can enhance next-day recognition of images when applied immediately after the images are viewed, neuroscientists have found.

The results were published by PNAS.

The findings are the first example of electrical brain stimulation in humans giving a time-specific boost to memory lasting more than a few minutes, the scientists say. Patients’ recognition only increased for stimulated images, and not for control images presented in between the stimulated images. The experiments were conducted at Emory University Hospital in 14 epilepsy patients undergoing intracranial monitoring, an invasive procedure for the diagnosis of seizure origin, during which electrodes are introduced into the brain.

“We were able to tag specific memories to be better remembered later,” says co-first author Cory Inman, PhD, postdoctoral fellow in the Department of Neurosurgery. “One day, this could be incorporated into a device aimed at helping patients with severe memory impairments, like those with traumatic brain injuries or mild cognitive impairment associated with various neurodegenerative diseases. However, right now, this is more of a scientific finding than a therapeutic one.”

“We see this as a platform for the further study of memory enhancement,” says senior author Jon T. Willie, MD, PhD, assistant professor of neurosurgery and neurology at Emory University School of Medicine. “The time specificity enables a lot of other experiments, since we know that there’s not a carry-over effect from one image to the next.”

Deep brain stimulation (DBS), with current delivered continuously by an implanted device, is an established clinical method for the treatment of movement disorders such as Parkinson’s disease, and is being tested for psychiatric conditions such as depression. In contrast with DBS’s invasiveness, researchers elsewhere have experimented with non-invasive electrical stimulation as an approach for enhancing memory or cognition, with several rounds of stimulation applied while learning.

“The advantage of DBS is that it can selectively modulate a specific brain circuit without broad off-target effects,” says Willie, who performed surgeries on patients in the study.

The amygdala’s key roles in emotional responses and fear-associated learning have been well-studied. So the Emory scientists made sure that amygdala stimulation at low levels of current (0.5 milliamps) did not result in emotional responses, an elevated heart rate, or other signs of arousal. Study participants reported that they did not notice the stimulation at any point in the study.

The researchers avoided direct stimulation of the hippocampus, figuring that would be too close to the machinery of memory itself, like introducing a live wire into a computer’s motherboard.

“We chose the amygdala because of decades of research in rodents, showing that it interacts with several other memory structures in a modulatory role,” says co-first author Joseph Manns, PhD, associate professor of psychology. “We wanted to stimulate its endogenous function, which we think is to signal salience – something standing out – so that specific experiences are remembered in the future.”

Manns and his colleagues had already shown that electrical amygdala stimulation increases rodents’ ability to recognize images later. The human experiments were designed to closely resemble how his lab’s tests with rodents were set up.

Study participants first viewed 160 neutral objects (emotional faces were excluded, for example) and were asked to judge whether the objects belonged indoors or outdoors. For half of the images, participants received stimulation for one second after each image disappeared from the screen. They were quizzed on half the stimulated images and half the unstimulated images immediately, and the other half the next day. 40 new images were used as decoys. The effect of stimulation on immediate recognition was not statistically strong. However, the next day, the effects on stimulated images were clear.

“This makes sense because the amygdala is thought to be important for memory consolidation - making sure important events stick over time,” Manns says.

79 percent of the participants (11 out of 14) showed an improvement on overnight memory tests, while the remaining 21 percent showed no improvement or impairment. When compared to no stimulation, the increase in number of images accurately recognized ranged from around 8 percent up to several hundred percent.

Some of the patients had impaired memory as a result of their epilepsy; the patients in whom a greater effect was seen generally had poorer baseline memory performance. For instance, one patient essentially forgot all of the control images, but maintained good memory for the stimulated images. However, a substantial effect was also observed in people who had an average memory to start with.

“The average was like having a ‘B’-level memory performance move up to an 'A’,” Willie says.

The researchers were also able to see signs of the previous day’s stimulation, in terms of electrical interactions within the brain, when those images were viewed again. The Emory team is now fine-tuning amygdala stimulation parameters, so that memory enhancement might be optimized. They are beginning to look at other types of memory tests, such as spatial or verbal tasks, as well as tasks that more closely mimic memory for real-world events.

“We want to understand the brain’s endogenous mechanisms for memory modulation better before moving ahead with a device,” Manns says.

Source:
http://news.emory.edu/stories/2017/12/amygdala_stimulation_memory/

Journal article:
http://www.pnas.org/content/early/2017/12/12/1714058114?sid=e6abd955-9a1e-49de-b1c0-2825b8bcdf78

#amygdala #electricalstimulation #deepbrainstimulation #memory #learning #neuroscience

Pillars of the Eagle Nebula in Infrared


Pillars of the Eagle Nebula in Infrared
Newborn stars are forming in the Eagle Nebula. Gravitationally contracting in pillars of dense gas and dust, the intense radiation of these newly-formed bright stars is causing surrounding material to boil away. This image, taken with the Hubble Space Telescope in near infrared light, allows the viewer to see through much of the thick dust that makes the pillars opaque in visible light.

The giant structures are light years in length and dubbed informally the Pillars of Creation. Associated with the open star cluster M16, the Eagle Nebula lies about 6,500 light years away. The Eagle Nebula is an easy target for small telescopes in a nebula-rich part of the sky toward the split constellation Serpens Cauda (the tail of the snake).

Image & info via APOD
https://apod.nasa.gov/apod/astropix.html
Image Credit: NASA, ESA, Hubble, HLA; Processing: Lluís Romero

#universe #space #NASA #nebula

Sunday, 17 June 2018

An Active Prominence on the Sun


An Active Prominence on the Sun
Sometimes the Sun's surface becomes a whirlwind of activity. Pictured is a time-lapse video of the Sun's surface taken over a two hour period in early May, run both forwards and backwards. The Sun's surface was blocked out so that details over the edge could be imaged in greater detail.

Hot plasma is seen swirling over the solar limb in an ongoing battle between changing magnetic fields and constant gravity. The featured prominence rises about one Earth-diameter over the Sun's surface. Energetic events like this are becoming less common as the Sun nears a minimum in its 11-year activity cycle.

Info & video via APOD
https://apod.nasa.gov/apod/astropix.html
Video Credit: Chuck Ayoub (Chuck's Astrophotography)
https://www.astrobin.com/users/YobSnob/

#universe #sun #space #science #NASA

Thursday, 14 June 2018

Noise sensitivity visible in brain structures


Noise sensitivity visible in brain structures
Recent functional studies conducted at the University of Helsinki and Aarhus University suggest that noise sensitivity, a trait describing attitudes towards noise and predicting noise annoyance, is associated with altered processing in the central auditory system. Researchers have found that noise sensitivity is associated with the grey matter volume in selected brain structures previously linked to auditory perceptual, emotional and interoceptive processing.

Having an increased amount of grey matter in these areas may mean that noise sensitivity requires more neural resources to be involved in dealing with sound.

“We found greater grey matter volume in people with high noise sensitivity in the brain temporal regions, as well as the hippocampus and the right insula. These cortical and subcortical areas are parts of brain networks supporting listening experience,” says researcher Marina Kliuchko, the first author of the research article published in NeuroImage journal.

The research included brain images of 80 subjects from which grey matter volume, cortical thickness, and other anatomical parameters were measured and correlated with noise sensitivity. The work brings new insight into the physiological mechanisms of noise sensitivity.

"Noise sensitivity may be related to self-awareness in noise-sensitive individuals about the sensations that noise induces in them. That is suggested from the increased volume of the anterior part of the right insular cortex, which is known to be important for matching external sensory information with internal state of the body and bringing it to one’s conscious awareness,” Kliuchko says.

Source:
https://www.helsinki.fi/en/news/health/noise-sensitivity-visible-in-brain-structures

Journal article:
https://www.sciencedirect.com/science/article/pii/S1053811917309734?via%3Dihub

#auditorycortex #noisesensitivity #graymatter #hippocampus #amygdala #neuroscience

Wednesday, 6 June 2018

The Clash of NGC 3256


The Clash of NGC 3256
Marked by an unusually bright central region, swirling dust lanes, and far flung tidal tails, peculiar NGC 3256 is the aftermath of a truly cosmic collision. The 500 million year old clash of two separate galaxies spans some 100 thousand light-years in this sharp Hubble view.

Of course when two galaxies collide, individual stars rarely do. Giant galactic clouds of molecular gas and dust do interact though, and produce spectacular bursts of star formation. In this galaxy clash, the two original spiral galaxies had similar masses. Their disks are no longer distinct and the two galactic nuclei are hidden by obscuring dust.

On the timescale of a few hundred million years the nuclei will likely also merge as NGC 3256 becomes a single large elliptical galaxy. NGC 3256 itself is nearly 100 million light-years distant toward the southern sailing constellation Vela. The frame includes many even more distant background galaxies and spiky foreground stars.

Image & info via APOD
https://apod.nasa.gov/apod/astropix.html
Image Credit & License: NASA, ESA, Hubble Space Telescope

#NASA #space ##galaxies #universe

Tuesday, 5 June 2018

Rolling ellipses of different dimensions to measure their perimeters.


Rolling ellipses of different dimensions to measure their perimeters. The red line is the curve of perimeter versus how squashed the ellipse is. The curve is defined by an elliptic integral, and cannot be expressed with elementary functions.

More:
http://dhushara.com/DarkHeart/QStad/QStad.htm

Work by matthen
http://blog.matthen.com/

#maths #science #geometry

A Sun Pillar over Norway


A Sun Pillar over Norway
Have you ever seen a sun pillar? When the air is cold and the Sun is rising or setting, falling ice crystals can reflect sunlight and create an unusual column of light. Ice sometimes forms flat, six-sided shaped crystals as it falls from high-level clouds. Air resistance causes these crystals to lie nearly flat much of the time as they flutter to the ground. Sunlight reflects off crystals that are properly aligned, creating the sun-sun-pillar effect. In the featured picture taken last week, a sun-pillar reflects light from a Sun setting over Fensfjorden, Norway.

Image & info via APOD
https://apod.nasa.gov/apod/astropix.html
Image Credit: Thorleif Rødland

#naturalphenomena #sunpillar #NASA

Age is a case of mind over matter. If you don't mind, it don't matter.


Age is a case of mind over matter. If you don't mind, it don't matter.
~S. Paige

Thank you all for the B-day wishes!

Sunday, 3 June 2018

3-D Mini Brains Accelerate Research for Repairing Brain Function


3-D Mini Brains Accelerate Research for Repairing Brain Function
The Houston Methodist Research Institute is making mini brains from human stem cells that put researchers on a fast track to repair the nervous system after injury or disease of the brain and spinal cord.

Houston Methodist neuroscientist Robert Krencik, Ph.D., and his team have developed a new system to reduce the time it takes to grow these brain models, which will give them the ability to screen drugs and study what’s behind disease-causing mutations more quickly. Their findings are described in an article titled “Systematic three-dimensional coculture rapidly recapitulates interactions between human neurons and astrocytes,” in Stem Cell Reports.

“We always felt like what we were doing in the lab was not precisely modeling how the cells act within the human brain,” Krencik said. “So, for the first time, when we put these cells together systematically, they dramatically changed their morphological complexity, size and shape. They look like cells as you would see them within the human brain, so now we can study cells in the lab in a more natural environment.”

And why is this important? Krencik says cells grown in traditional lab cultures are put on a flat petri dish, broken up and otherwise manipulated, disturbing their interactions. This results in not being able to reproduce the form, structure and developmental growth of the brain’s cells in the lab, leading to very simplistic-looking and immature cells. In the human brain, however, these cells are very complex-looking and interact in intricate ways with each other and the environment. New technologies are now focused on 3-D culture systems, but the exhaustive time for these studies is not feasible for accelerating discoveries.

“Normally, growing these 3-D mini brains takes months and years to develop,” Krencik said. “We have new techniques to pre-mature the cells separately and then combine them, and we found that within a few weeks they’re able to form mature interactions with each other. So, the length of time to get to that endpoint for studies is dramatically reduced with our system.”

Krencik’s lab focused on a star-shaped cell type called astrocytes, because they are a key factor in getting the brain’s neurons to connect and talk to each other by helping to increase the number and strength of neuronal connections in the brain and spinal cord. They are involved in most neural diseases and also are responsible for maintaining a healthy nervous system. With the model Krencik’s team bioengineered, the incorporation of astrocytes accelerated the connections of the surrounding neurons.

Krencik’s group is the first to specifically engineer astrocytes into these 3-D mini brains. By doing so, this led to the accelerated maturation of both the astrocytes and the surrounding neurons. Introducing them for the first time in this paper, he coined these bioengineered mini brains “asteroids” to distinguish them from other types of 3-D sphere cultures, known as organoids. Krencik’s “asteroids” contain specific populations of astrocytes, whereas organoids have undefined numbers and types of cells.

“Using our system, we can generate mature astrocytes and have them interact intimately with neurons to a greater extent than has been done before,” Krencik said. “Unlike other cells in the brain and in the rest of the body, astrocytes have unique properties in humans. It’s thought they are partly responsible for the unique cognitive functions of humans and also may underlie aspects of human diseases, such as Alzheimer’s and autism spectrum disorders.”

Ultimately, Krencik is using these “asteroids” to form functional neural circuits that researchers can experimentally manipulate for developing treatments and deciphering what makes diseases tick. Krencik says they can make induced pluripotent stem cells, commonly termed iPS cells, from any disease or patient and then form these mini brains to study the disease process, as well as screen therapeutic compounds on them to aid in the development of drugs. Within about five years, his goal is to use this system to develop clinical trials to improve or regenerate a person’s impaired nervous system.

Source:
https://www.houstonmethodist.org/newsroom/3-d-mini-brains-accelerate-research-for-repairing-brain-function/

Journal article:
https://www.cell.com/stem-cell-reports/fulltext/S2213-6711(17)30481-2

#astrocytes #neurons #pluripotentstemcells #brainfunction #neuroscience