UCLA Scientists Count Cells with Stereo Investigator in Study Identifying Compensating Regions in Brain Damage


If one area isn’t working, another part can step in. Plasticity is one of the brain’s most beautiful attributes. Recent research has documented the organ’s ability to compensate in the face of damage, and now a new study identifies a key region for compensation when the damage occurs in the hippocampus.

The region is the medial prefrontal cortex (mPFC). It’s an integral part of the hippocampal-prefrontal-amygdala circuit involved with memory formation – specifically with contextual fear memories. In their study, published last month in Proceedings of the National Academy of Sciences, researchers at the University of California, Los Angeles identify a microcircuit in the mPFC that can encode memories when the dorsal hippocampus is damaged.

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Increased Choline During Pregnancy Improves Learning in Down Syndrome Mice

DCX Cells Counted With Stereo InvestigatorObstetricians and midwifes have long hailed the benefits of folic acid during pregnancy. Now new research offers evidence that choline is another important nutrient for the developing fetus. Found in foods like eggs and cauliflower, choline is known to aid healthy liver function. But in the past few years, studies have shown that the nutrient also plays a role in brain development. One recent study by Velasquez and colleagues claims that increased choline during pregnancy may offer a possible therapy for Down syndrome.

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Study Links Increased Touch to Enhanced Neurogenesis in Adult Mice; Stereo Investigator Used for Quantification


According to scientists at the Hotchkiss Brain Institute in Calgary, Canada, there is evidence for increased neurogenesis in adult mice reared by two parents. Their study also describes other interesting findings, such as the fact that increased neurogenesis persists in the next generation, or that the effects of differences in rearing affect males and females differently.

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Wisconsin Scientists Use Stereo Investigator to Quantify Neurons Formed From Stem Cells


Researchers at the Waisman Center (University of Wisconsin-Madison) just took a big step in their quest to develop regenerative medicines for treating Parkinson’s, Alzheimer’s, and other neurodegenerative diseases. They used human embryonic stem cells to restore memory and learning in disabled mice.

The study, published last month in Nature Biotechnology, “is the first to show that human stem cells can successfully implant themselves in the brain and then heal neurological deficits,” senior author Su-Chun Zhang told the University of Wisconsin-Madison news department.

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Neurolucida & Stereo Investigator Help Uncover Cerebellar Granule Cells’ Role in Muscle Memory


Learning a new dance routine or how to ride a bike is possible because of Cerebellar Granule Cells (GCs) according to Galliano and colleagues in The Netherlands. To find out more about the role of these abundant brain cells, and why we have so many of them, the scientists silenced most of the GCs in a group of mutant mice. They found the rodents could balance and run as well as they ever did, but when it came to learning new activities involving motor function, the mice had a harder time.

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Stereo Investigator Contributes to Study Showing Low Zinc Levels Associated With More Cell Deaths in Spinal Cord Injury


Spinal cord injuries can result in a range of physical disabilities from slight loss of motor function to major paralysis, but little is known about the mechanisms underlying the damage. Scientists affiliated with the Miami Project to Cure Paralysis at the University of Miami are gaining knowledge about how the nervous system responds to spinal cord injuries. Their latest study, published last month in the Journal of Neuroscience Research, suggests that post trauma cell death is associated with low zinc levels.

“The expression of functional NF-kB signaling resulted in a reduction in extracellular zinc levels, thereby inducing glutamate-induced cell death,” the authors say in their paper “Reduced Extracellular Zinc Levels Facilitate Glutamate-Mediated Oligodendrocyte Death After Trauma.

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Stereo Investigator Helps Scientists Assess Damage in Rat Model of Ischemic Stroke


A stroke patient is rushed to the hospital. Deprived of oxygen-rich blood, brain cells have already died, and more damage will probably occur in the hours and days to come. But researchers at the University of South Florida and the University of Padova in Italy say a two-part package administered through the body, rather than directly into the brain, may be the key to staving off some of the cell death that takes place after a stroke.

In their study, published in the Journal of Enzyme Inhibition and Medicinal Chemistry, the scientists saw a smaller region of damage in a rat model of focal cerebral ischemia, when the rats were treated with a combination of an anesthetic and a Caspase-3 inhibitor – a drug that suppresses a protein involved in brain cell death.

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Florida Researchers Study Traumatic Brain Injury With Stereo Investigator


Figure 3 from “Hippocampal CA3 cell loss and downregulation of cell proliferation.”

If a head gets hit hard enough, the trauma occurs instantly. Neurons die, the brain swells as microglia cells rush to the damaged area, and the protective armor known as the blood brain barrier might even rupture. But it doesn’t end there. Long term effects include cognitive impairment, loss of sensory processing, and susceptibility to neurodegenerative diseases like Alzheimer’s.

Researchers at the University of South Florida say patients suffering from chronic Traumatic Brain Injury (TBI) experience a “cascade of events” marked by long-term neuroinflammation, cell loss, and impaired cell proliferation that may manifest over time.

“While TBI is generally considered an acute injury, a chronic secondary cell death perturbation (i.e., neuroinflammation) and a diminished endogenous repair mechanism (i.e., cell proliferation) accompany the disease pathology over long-term,” the authors say in their paper published this month in PLOS ONE.

The scientists used unbiased stereology to analyze activated microglia cells, cell proliferation, and differentiation into immature neurons in several regions of the brains of rats which had experienced TBI eight weeks prior.

They used Stereo Investigator with the Cavalieri estimator probe and the optical fractionator probe to estimate the quantity and volume of stained cells in the cortex, striatum, thalamus, fornix, cerebral peduncle, and corpus callosum, as well as the subgranular zone and the subventricular zone in both hemispheres of the brain.

Eight weeks after the TBI occurred, the researchers found an increased level of active microglia cells at the direct site of the TBI as well as surrounding regions. They also report a decrease in hippocampal neurons, and low levels of cell proliferation in the neurogenic niches.

“Our overarching theme advances the concept that a massive neuroinflammation after TBI represents a second wave of cell death that impairs the proliferative capacity of cells, and impedes the regenerative capacity of neurogenesis in chronic TBI,” the authors say in their paper.

They go on to suggest a “multi-pronged treatment targeting inflammatory and cell proliferative pathways” may help alleviate the pathological effects of chronic TBI.

Read the full paper “Long-Term Up-regulation of Inflammation and Suppression of Cell Proliferation in the Brain of Adult Rats Exposed to Traumatic Brain Injury Using the Controlled Cortical Impact Model” on PLOS ONE.

{Acosta S.A., Tajiri N., Shinozuka K., Ishikawa H., Grimmig B., et al. (2013). Long-Term Up-regulation of Inflammation and Suppression of Cell Proliferation in the Brain of Adult Rats Exposed to Traumatic Brain Injury Using the Controlled Cortical Impact Model. PLoS ONE 8(1): e53376. doi:10.1371/journal.pone.0053376}

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Scientists at Duke Say Mice Have Features Associated With Vocal Learning


Dr. Erich Jarvis spends a lot of time with songbirds. At his Duke University lab, Jarvis, a Stereo Investigator user, studies the neurobiology of vocal communication. Since his feathered friends learn song much like humans learn speech, they’re a favorite model. But Dr. Jarvis says mice sing too, and new research says they can learn new tunes.

“We investigated the mouse song system and discovered that it includes a motor cortex region active during singing, that projects directly to brainstem vocal motor neurons and is necessary for keeping song more stereotyped and on pitch,” the authors said in their study published in PLoS ONE.

The discovery is controversial as it challenges longstanding beliefs that mice can not learn vocal behavior, but if Dr. Jarvis’ findings are true, it will be a breakthrough for scientists studying autism and anxiety disorders, according to a Duke University press release.

“The researchers who use mouse models of the vocal communication effects of these diseases will finally know the brain system that controls the mice’s vocalizations,” Dr. Jarvis said in the press release.

While studying speech evolution in humans, Dr. Jarvis and his colleagues tested male mice for vocal learning – an ability only believed to be shared by humans, songbirds, parrots and hummingbirds.

The research team used gene expression markers to see which neurons fired in the motor cortex when the mice sang. The researchers then damaged these neurons, and found the mice could no longer stay on pitch. Using an injectable tracer, they mapped a signal pathway from the motor cortex, through the brainstem, to the larynx muscles.

To test whether mice could learn vocalizations, the researchers placed pairs of male mice in a cage with one female mouse. After seven to eight weeks, the male mice had changed their tunes so they were singing the same pitch.

“Our results show that mice have the five features scientists associate with vocal learning. In mice, they don’t exist at the advanced levels found in humans and song-learning birds, but they also are not completely absent as commonly assumed,” he said.

Read about the study on Duke TODAY and CBS News, and read the full paper at PLoS ONE.

“Of mice, birds, and men: the mouse ultrasonic song system has some features similar to humans and song-learning birds,” Arriaga, G. et. al. (2012) PLOS ONE. 7(10): e46610. doi:10.1371/journal.pone.0046610

[Image via the Erich Jarvis Lab website]

Stereo Investigator Helps Harvard Scientists Study Social Isolation’s Effects on the Brain

Some children raised in orphanages grow up to develop social disorders, and there’s not all that much modern medicine can do about it. But scientists at Harvard Medical School are working on gaining a better understanding of how early isolation affects a developing brain. Their research gives new insight into the mechanisms at play, and indicates that timing and healthy myelination are crucial.

“Social isolation from P21 to P35 alters [medial Prefrontal Cortex] oligodendrocyte morphology, myelination, and mPFC-mediated behaviors,” the authors say in their paper, published in Science. “These effects persist even when isolated mice are re-exposed to social interactions, which suggests a link between the quality of mPFC myelination established during the juvenile period and adult behaviors.”

Led by Dr. Manabu Makinodan, the research team studied three groups of male mice. At 21-days-old, the mice were caged according to different scenarios: isolated environment (alone),  regular environment (with three other mice), or enriched environment (with seven other mice and a selection of toys). Four weeks later, testing showed deficits in social behavior and memory in the isolated mice.

To determine what went wrong in the brains of the isolated mice, the researchers examined the oligodendrocyte neurons in the prefrontal cortex, a brain region integral to social behavior. They determined that the density of oligodendrocytes was the same in all three groups, by using Stereo Investigator with the optical disector to perform a stereological count. Although density was consistent, the morphology of oligodendrocytes in the brains of the isolated mice was remarkably different. These mice displayed a simpler morphology that included “shorter processes, less branching, and fewer internodes.” Their myelin sheaths were thinner, resulting in decreased signaling between neurons and altered information processing.

Further trials showed that mice isolated later in life, after 35 days of age, showed the same morphology as normally reared mice, indicating that the critical period for development is before 35 days. They also noticed that mice isolated from 21 days, and which were later returned to normal environments, still showed abnormal morphology, implying that the detrimental effects of isolation could not be reversed.

“Our findings indicate that the effects of childhood isolation and neglect on adult mental health might be caused, at least in part, by alterations in oligodendrocytes and myelin development. Furthermore, we provide a cellular and/or molecular context and genetic models in which to begin to understand the effects of juvenile social experience on brain development in general and myelin maturation in particular. Our results also may be relevant to neuropsychiatric disorders such as schizophrenia and mood disorders” (Makinodan, et al, 2012).

Access the paper “A Critical Period for Social Experience–Dependent Oligodendrocyte Maturation and Myelination” at ScienceMag.org.

Manabu Makinodan, Kenneth M. Rosen, Susumu Ito, and Gabriel Corfas. “A Critical Period for Social Experience–Dependent Oligodendrocyte Maturation and Myelination.” Science, 2012; 337 (6100): 1357-1360 DOI: 10.1126/science.1220845

Image of Oligodendrocyte courtesy of Harvard Medical School.