What are organoids?: A Mint on Sunday audio story – Livemint

Stem cells have the unique property of developing into any cell of the body under the right conditions. For this reason, there is a growing interest in using them to treat disorders such as hemophilia, diabetes and even neurodegenerative disorders such asParkinsons.

Apart from their therapeutic potential, researchers have shown that stem cells can be coaxed to spontaneously develop intominiature organ like structures called "organoids".Organoids recapitulate the intricate physical and biological features of organs and hence are important new tools in understanding human tissue development as well as for finding new drugs to treat disorders.

In this podcast, we discuss the biology of organoids, the hope and hype in medical research as well as potential ethical issuessurrounding their use.

This podcast is written and produced by IndSciComm, a collective of Indian scientists working on increasing public science awareness.

Shruti Muralidhar is a postdoc at the Picower Institute for Learning and Memory at MIT studying how memory is encoded in the brain.

Navneet Vasistha is a postdoctoral researcher at the University of Copenhagen trying to understand the cellular basis of mental health disorders.

Abhishek Chari is a science writer at the Picower Institute for Learning and Memory at MIT with an interest in microbiology and evolution.

(Scroll down past the references to read a transcript of the podcast.)

References and further reading

Skin transplants:

Serial Cultivation of Strains of Human Epidermal Keratinocytes

Grafting of Burns with Cultured Epithelium Prepared from Autologous Epidermal Cells

Cerebral organoids:

Cerebral organoids model human brain development and microcephaly

Pituitary organoids and functional restoration:

Self-formation of functional adenohypophysis in three-dimensional culture

Proto-tooth organoids:

The development of a bioengineered organ germ method

Fully functional bioengineered tooth replacement as an organ replacement therapy

Energy and entropy in living systems:

Energy and entropy flows in living systems

The Science of Self-Organization and Adaptivity

The Ilya Prigogine Nobel Prize

Self-organization in different scientific fields:

The science of self-organization and adaptivity

Self-organization in economics:

From simplistic to complex systems in economics

Self-organization in social sciences:

Self-organization and social science

Protein folding as self-organization:

Self-organization in protein folding and the hydrophobic interaction

Self-organization of cytoskeleton:

Directed cytoskeleton self-organization

Biofilm self-organization:

Self-Organization, Layered Structure, and Aggregation Enhance Persistence of a Synthetic Biofilm Consortium

Antibiotic resistance in biofilms:

Mechanisms of antibiotic resistance in bacterial biofilms

Biofilm formation evades immune system:

Biofilm Formation Avoids Complement Immunity and Phagocytosis of Streptococcus pneumoniae

Biofilms on teeth:

Oral Biofilm Architecture on Natural Teeth

Biofilms in catheter-associated UTIs:

Role of biofilm in catheter-associated urinary tract infection

Model system limitations / Self-organization in embryos and ethical issues:

Self-Organization of Stem Cell Colonies and of Early Mammalian Embryos

Comparisons between tissue cultures and embryo development:

In vitro organogenesis in three dimensions: self-organising stem cells

Categories of self-organization:

Cytosystems dynamics in self-organization of tissue architecture

Importance of apoptosis in embryo development:

Cell death in development: shaping the embryo

Optic cup organoid:

Self-formation of optic cups and storable stratified neural retina from human ESCs

Intestinal organoids:

Establishment of Human Colon Culture System

Intestinal OrganoidsCurrent and Future Applications

14-day rule:

Embryology policy: Revisit the 14-day rule

Early embryos in a dish (commentary):

What if stem cells turn into embryos in a dish?

Early embryos in a dish (research articles):

A method to recapitulate early embryonic spatial patterning in human embryonic stem cells

Ethical issues in human organoid and gastruloid research

The Ethics of Organoids: Scientists Weigh in on New Mini-Organs

Organoids are more like fetal or neonatal organs, not adult organs:

Human cerebral organoids recapitulate gene expression programs of fetal neocortex development

hPSC-derived lung and intestinal organoids as models of human fetal tissue

Organoids and the Zika virus:

The High Schooler Behind the Mini-Brain Generator

Cold Spring Harbor grant for 3D cancer organoids:

CSHL to lead international team developing next-generation organoid cancer research models

Conclusion:

Cutting-edge stem cell therapy proves safe, but will it ever be effective?

Transcript of the podcast

Navneet: A long time ago, in a galaxy far, far... Wait, is that how were starting this podcast? No, actually in 1975, at the Massachusetts Institute of Technology, scientists James Rheinwald and Howard Green developed a method by which they could indefinitely grow human skin in the lab!

This is the first report of scientists being able to grow an organ in the lab. Their litmus test came five years later, when they were asked to treat two patients admitted to the Brigham Hospital with significant burns. Not only were Green and his colleagues able to graft skin sheets grown from the patients own cells, but in six months time, these grafts could no longer be distinguished from the surrounding unburnt skin.

Attempts at growing other organs have not met with a similar degree of success, for a variety of reasons.

However, with recent advances in stem-cell biology, researchers have found that by growing stem cells in just the right way, they can produce tiny blobs of tissue that look and function like organs.

Depending on what molecular cues are added, scientists have been able to grow what can lazily be called mini-brains, mini-pancreas, mini-retinal tissues, etc. The collective term given to these lab-grown tissues is organoids. My name is Navneet.

Abhishek: Im Abhishek.

Shruti: This is Shruti.

All: And we are IndSciComm. In this podcast, were going to be talking about what these organoids are and what they are not, how close are they are to actual organs, what their future potential is and a whole host of other interesting things.

***

Navneet: So, lets begin with the basics. What are organoids and why are they interesting?

a. An organoid is a three-dimensional mass of cells that superficially resembles an organ or a gland. Researchers have generated several kinds of organoids using what they know about the development of different organs. Some examples are cerebral or brain organoids, intestinal organoids, pituitary organoids and so on.

b. Essentially, what makes them interesting is that cells grown in a dish with the right nutrient and cell growth factors can form something like mini-organs.

c. Some organoids have been transplanted into mice to restore functions or structures that they are lacking. For example, transplanted pituitary organoids have helped to restore the function of dysfunctional pituitary glands in mice. In fact, scientists have even transplanted a proto tooth organoid into the mouth of an adult mouse and watched it develop into a fully grown tooth!

***

Abhishek: So, cells can form structures of higher complexity like organoids. In essence, simple things (cells) come together to form more complex things (organs). This phenomenon is called self-organization. But how is this possible? Doesnt the second law of thermodynamics say that entropy has to increase over time?

How can order be created out of chaos, if entropy can only be increased? Entropy, by the way, is just the technical term for randomness. The solution is to rearrange the system using energy. Any decrease in entropy in one part of the system can be compensated by a proportionally larger increase in entropy in another part of the system.

As a simple analogy, consider the problem of cleaning your room. One way is to throw everything thats lying around into a cupboard. The room definitely looks more ordered but that doesnt detract from the mess inside the cupboard. Therefore, you havent reduced the net entropy of the systemyou have merely re-distributed it.

This isnt just some quirky, obscure thermodynamics loophole. A Nobel Prize in Chemistry was given for understanding how order can be generated from disorder, to Ilya Prigogine in 1977.

So, there is a theoretical basis to explain the origin of complexity in our universe. Self-organization as a phenomenon has been studied in physics, chemistry, biology and many other disciplines, including economics and sociology.

Now, getting back to the point. The three of us, we are all biologists by training. And just to remind our listeners, we still want to talk about organoids. So, lets work our way up to organoids by showing you how self-organization is necessaryright from the level of molecules to the level of the organism.

At the simplest level, we have molecules that can self-organize into more complex configurations. This happens with proteins, that are formed as a long, disorganized chain of amino acids. But, they fold themselves into complex nanomachines. Some of these can juggle atoms between other molecules, acting as catalysts for important biological reactions.

Next, molecules can self-organize into mega-structures that form important components in cells. Polymerization of small molecules helps to form the protein-based skeleton inside cells and the protein coats of some viruses.

Moving up from molecules, even apparently simple organisms like bacteria can self-organize themselves into marvels of biological architecture called biofilms. In this combined state, bacteria in biofilms can resist antibiotics, fight off the immune system and demonstrate feats of resilience that single cells are incapable of. You can blame biofilms for everything from the gunk on your teeth after a good nights sleep, to entrenched catheter infections and many other things in between.

All organisms are dependant, to varying degrees, on self-organization to make them what they are. Every multicellular organism, all the way from slime molds to plants and animals, starts off life as a single cell that has to replicate itself to make an embryo.

***

Shruti: The early embryo is a mass of stem cells without the defining features of a multicellular organismlike a head, tail, limbs and so on. Provided they get the right cues or signals, these stem cells are capable of forming a complete organism. Researchers study these cues and other steps in embryo development using animal models like mice.

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What are organoids?: A Mint on Sunday audio story - Livemint

Study identifies new genetic risk factor for developing autism spectrum disorder – Medical Xpress

Brian J. O'Roak, Ph.D., assistant professor of molecular and medical genetics, OHSU, January 4, 2017. Credit: OHSU/John Valls

Autism spectrum disorder affects approximately one out of every 68 children in the United States. Despite expansive study, the origin and risk factors of the complex condition are not fully understood.

To better understand the root causes, an international team led by researchers at OHSU in Portland, Oregon has applied a new systematic analysis to a cohort of 2,300 families who have a single child affected with autism. The study focused on identifying and characterizing low-lying genetic mutations that may have been missed in previous research, given these mutations are only present in a fraction of the bulk DNA of an individual.

Known as postzygotic mosaic mutations, or PMMs, these genetic changes occur after the conception of the human zygote during the development cycle of a fetus. An individual will contain a mosaicor assortmentof mutated and non-mutated cells with the level of mosaicism depending on the time and location of the mutation's occurrence. This emerging class of genetic risk factors has recently been implicated in various neurologic conditions, however, their role in more complex disorders, such as autism, has been unclear.

Autism risk due to unexpected mosaic mutations

By comparing genetic sequencing data of these familiespart of the Simons Simplex Collection, a permanent repository of precisely characterized genetic samplesthe research team determined that approximately 11 percent of previously reported new mutations affecting a single DNA base, which were thought to have be present at the time of human conception, actually show evidence of the mutation occurring during the development process.

"This initial finding told us that, generally, these mosaic mutations are much more common than previously believed. We thought this might be the tip of a genetic iceberg waiting to be explored," said the study's principal investigator Brian O'Roak, Ph.D., an assistant professor of molecular and medical genetics in the OHSU School of Medicine.

To investigate this possibility, a custom approachleveraging next generation sequencing and molecular barcodes - was developed to both identify these low-level mutations, and also validate that they are, in fact, real and not technological artifacts. With this more sensitive method, the rate of potentially PMMs increased to 22 percent of the new mutations present in children.

The researchers then compared the rates of PMMs that result in different predicted effects on the genome in affected children and their unaffected siblings. This lead to an unexpected finding that so-called "silent" mosaic mutations were enriched in the affected children, contributing risk to approximately 2 percent of the individuals with autism in this cohort. These types of mutations are generally believed to be neutral, as they don't alter the genetic coding of proteins. However, the team found evidence that these mutations might actually be altering how genetic messages are stitched together.

The study also found preliminary evidence that mosaic mutations that alter the protein code of genes essential for development, or genes that resist mutations, are also enriched in individuals with autism. This contributes risk to an additional 1 to 2 percent of individuals with autism. Many of the PMMs occurred in some of the most highly validated autism risk genes identified to date, further suggesting that these mutations are contributing to autism genetic risk. Due to this, the research team believes that overall, mosaic mutations may contribute to autism risk in 3 to 4 percent of this cohort.

Understanding the timeline and location of mosaic mutations

Determining exactly when and where these mutations are occurring during development is challenging. The PMMs identified were present in 10 to 75 percent of the cells examined from the children's blood, suggesting that they likely occurred early in development. However, the exact timeline was not known.

By leveraging the unique family design of the Simons Simplex Collection cohort, O'Roak's team analyzed the parents' genomes and discovered that 6.8 percent of the supposedly "new" mutations present in children at conception could actually be traced back to a PMM that occurred early in the development of their parent. These mutations were generally present in 20 to 75 percent of the parents' blood cells, providing indirect evidence that many of the PMMs occurring in children did in fact happen very early during development and that they likely contribute mosaicism across the body, including in the brain.

"In addition to a need for broader research focused on the role that mosaicism plays in autism and related disorders, our data argue that physicians should be requiring more sensitive testing of both children and parents, when a new disorder-related genetic mutation is identified," O'Roak said. "These mutation can go from being in a few percent of the cells of a parent to 100 percent of the cells of a child. If present, at even low levels in the parents, the risk of additional children receiving this mutation is dramatically increased."

"Exonic mosaic mutations contribute risk for Autism Spectrum Disorder" published today in The American Journal of Human Genetics.

Explore further: Late-breaking mutations may play an important role in autism

More information: Deidre R. Krupp et al. Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder, The American Journal of Human Genetics (2017). DOI: 10.1016/j.ajhg.2017.07.016

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Study identifies new genetic risk factor for developing autism spectrum disorder - Medical Xpress

Rush testing if genetic clues identify best candidates for Parkinson’s surgery – Medical Xpress

Rush Neurologist Gian Pal, MD, MS, the primary investigator for the National Institute of Health-funded clinical study Parkinson disease and DBS: cognitive effects in GBA mutation carriers. Credit: Rush Photo Group

In the first ever clinical investigation involving genetic screening for Parkinson's disease, researchers are testing whether the presence of a specific genetic mutation identifies which patients are the best candidates for deep brain stimulation surgery, and whether neurologists should perform that procedure differently based on that genetic information.

"We are at a very promising time in Parkinson's disease (PD) research. Finding the connections between the vast amounts of genetic data and cognitive data we are gathering will allow us to tailor future therapies based on genetic biomarkers," said Rush neurologist Gian Pal, MD, MS, the primary investigator for the National Institute of Health-funded clinical study "Parkinson disease and DBS: cognitive effects in GBA mutation carriers"

Deep brain stimulation (DBS) is a surgical procedure in which a battery-operated medical device implanted in the brain delivers electrical stimulation to specific areas in the brain that control movement, thus altering the abnormal signals that cause many PD motor symptoms.

DBS is typically used for individuals whose symptoms cannot be adequately controlled with medication and has proven to dramatically improve motor function and potentially reduce medication burden for many PD patients.

Research suggests that patients who carry a mutation in the glucocerebrosidase (GBA) gene may respond differently to DBS than those who do not carry the mutation. These GBA mutation carriers compose 10-17 percent of subjects undergoing DBS, and typically have higher deposits of alpha-synuclein protein in the brain. Abnormal accumulation of alpha-synuclein is thought to be a key reason for the development and progress ion of PD. These higher levels of alpha-synuclein in patients with the GBA mutation carriers may translate to even more problems with thinking, movement, behavior, and mood than expected in typical PD. Dr. Pal and colleagues are hoping to understand how DBS affects motor function and cognition in these GBA mutation carriers over time.

"If we can determine how GBA mutation carriers respond to DBS, we can better counsel patients on expectations from the surgery, and potentially target a different region of the brain to maximize the benefit and minimize side effects from the surgery. This would be the first time that genetics would inform a clinical decision in the field of PD"

"Deep brain stimulation is a tremendous option for many Parkinson's disease patients, but not all," said Pal, who is developing a programmatic line of research involving genetics and surgical treatments for PD at the Rush Parkinson's Disease and Movement Disorders Program.

The Rush Parkinson's Disease and Movement Disorders Program is one of the largest and oldest such centers in the country, treating more than 2,000 patients annually. Rush has been a longstanding Parkinson's Disease Foundation Center of Excellence, based on decades of clinical and research excellence, and is now also recognized as a National Parkinson Foundation Center of Excellence as well.

Explore further: Drug discovery: Alzheimer's and Parkinson's spurred by same enzyme

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Investigating the neuroscience of contagious yawns – Medical News Today

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Baba Brinkman, comedy review: Comedy, hip hop and neuroscience will make your brain buzz – Evening Standard

Is it a comedy gig? A hip hop gig? A neuroscience lecture? Baba Brinkman's Rap Guide To Consciousness is all three. You may well walk out laughing, humming and wondering if you are a human being or a robot.

Leave any Vanilla Ice expectations in the cloakroom and imagine if Eminem had read philosopher Daniel Dennett. Brinkman wittily weaves together accessible ideas and inventive rhymes. Discussing artificial intelligence he sings "From Aristotle to Thomas Aquinas, people thought if you wanted design, you need a mind first."

The locquacious Canadian employs case studies in an attempt to clarify what consciousness is. In one adorably cute sequence he raps about his new baby Dylan, while an image of his smiling offspring flickers onscreen. Has Dylan got self-awareness yet? And if so did he have it as a tadpole-like embryo, dad asks.

There is lots to take in. Is there free will or are we all just glorified machines, slaves to our firing neurones? Apparently most of you reading this will have a "Jennifer Aniston neurone", triggered whenever you think of the Friends star, whether you like it or not.

Sara Pascoes favourite comedy venue, and with good reason: the Soho Theatre is arguably Londons finest place to see both up-and-coming and established acts. Being a theatre, rather than a comedy club per se, expect to see full sets from individuals rather than bills with a few comics. Its three rooms host all sorts of things, from the latest Edinburgh winners to big names road-testing their latest bits. The standard is reliably excellent: even if youve never heard of a comedian, chances are, if theyre playing here, theyll be worth watching.

Another old favourite, the Comedy Store benefits from being built for purpose: no other venue in London suits stand-up quite so well (and the beer isnt too ridiculously priced, either). After starting out above a strip club in Soho, this place made its name throughout the eighties by breaking the pioneers in alternative comedy. Its happy to host mainstream stars these days, and never struggles to draw top acts, but if you can only make one thing, try The Comedy Store Players, old pros whose improvised shows on Wednesdays and Sundays all but guarantee hilarity. Tuesdays The Cutting Edge is best for those who like topical humour.

Old Rope is popular with circuit veterans and newbies alike, so the weekly show usually has a mix of big names, comedy veterans and ones-to-watch. Host Tiff Stevenson leads an evening of new material yes, lots of jokes given their test run and its given its name for the noose that hangs over the stage. Ironically, this noose is a bit of a life-saver: if the new act is going badly, comics can grab the rope and fall back on old material.

Always top value, the Knock2bag nights offer the chance to indulge in the odder end of the comedy spectrum: expect serious helpings of whimsy, eccentricity and surrealism. If you're looking for something different, this is your place to go.

A first-rate comedy club and well worth travelling for. Wed pick the Thursday night over Saturday, but youll get a decent show on either day. Theres a mix of big names and up-and-comers, and host Martin Besserman is a pro wholl keep you laughing in between acts. Of which, theres often as many as twelve a night, so youll get your moneys worth. If one isnt to your taste, another promises a laugh.

The Banana Cabaret Club hosts a lot of top drawer comics, and is well loved in comedy circles in part, because theyve been going a good thirty years and in part because of the man running things, David Vickers, whose had everyone from Eddie Izzard to Stephen K Amos performing. Stars pop-in, and comedy circuit regulars play often, but its also on the finest spots to see new talent . No wonder Marcus Brigstocke name-checked it as his favourite London comedy club. Besides, once the two-hour show is done (typically wrapping up around 11pm), DJs strike up and everyone dances till 2am. Splendid.

http://vivivi.co.uk/

Hats off to the Piccadilly for keeping comedy cheap: their shows cost 10 at the most, and they do a meal deal, where you can eat at Tiger Tiger and see the show for 20 all-in. A bargain. Expect a mix of well-known TV regulars alongside the best newcomers on the scene. Line-ups are particularly well thought out here: they dont just sling together anyone, so the nights tend to be uniformly excellent.

The Leicester Square Theatre draws the big names, so expect to see top flight acts: Richard Herring hosts a weekly podcast here on Wednesdays, and the likes of Bridget Christie, Micky Flanagan and Frankie Boyle all make it a stopping point on their tours. That said, check the website for whats upcoming there are chance to see some under-the-radar sets too.

The excellent Brasserie Zdel whose Bar Americain is one of the finest drinking spots in the capital relaunched Crazy Coqs as Live At Zdel last year and following a successful first run, are launching their second season. Besides comedy the standard is usually very decent they also host musical theatre and drag acts. The cocktails are terrific and there's at-table service. Eat in the restaurant beforehand (or after), too: we swung by recently and the food is as good as its ever been. Cheap, too.

This fortnightly show boasts the best new up-and-coming acts in the capital, combined with big name hosts expect the likes of Miles Jupp, Sara Pascoe and Holly Walsh who keep the standard up to scratch. Definitely up to par, somewhere to find your new favourite comedian.

Just how a comedy club should be: small, crowded and above a pub. Best of all, its free, and each night offers something different, from open-mic nights to well-known names giving their latest sets an airing. Check the website for details, but you wont be let down just get down early, as it fills up quickly.

Following a decade of success in Shepherd's Bush, this comedy club has found a new home at the ever-popular Roof Gardens. Known as 'Jimmy Carr's favourite comedy club', the Ginglik has had everyone from Al Murray to Robin Williams play, and is set for more success.

The likes of Stewart Lee, Reginald D Hunter and Tony Law play these nights, which gives an idea of just how decent they are. Laugh Out London always do a good job of bringing the highlights from Edinburgh festival to town, so take the chance to see who everyones been tweeting about.

This Leicester Square club is much, much better than you might expect for a place that continually flyers. A big favourite with the Chortle Awards, it always attracts big names it runs a little like Live At The Apollo but on a smaller scale. There are three acts a night, and shows are fairly priced: some are as cheap as a fiver, though most will cost around 10 - 15. Theyve also got venues in Soho and Covent Garden.

Bit of a shame that shows here are so few and far between usually about once a month but theres no place more beautiful than the Union Chapel to see comedy in London. The upside is that, with so few performances, they always get the big names headlining, with unfailingly impressive support. Plus theres usually a live band, who are fab. The atmosphere is everything.

Anthony Devlin/PA Wire

These various plates are kept spinning thanks to Brinkman's enthusiasm and amiability. He is not the world's coolest rapper, but he might be the funniest and most well-read. Exercise any free will you have and buy a ticket.

Until Sept 3, 2 Northdown; tickettext.co.uk

Are you a budding artist? Enter the Evening Standard Contemporary Art Prize in association with Hiscox and you could win 10,000. Visit standard.co.uk/artprize

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Baba Brinkman, comedy review: Comedy, hip hop and neuroscience will make your brain buzz - Evening Standard

Neuroscience marks end of inaugural summer research experience for 18 undergrads – Augusta Free Press

EngelNovitt has maintaineda longstanding commitment to activelysupporting the College of Science, its pioneering research and novel degreeprograms that benefit Virginia Tech, its students, and the research community more broadly, said John Engel, manager of EngelNovitt. As soon as the School of Neuroscience and its neuroscience degree programs were announced, we wanted to broaden that support to include theEngelNovitt Undergraduate Research Fellowship to enable undergraduates to benefit even more directly in theadvancement of the schoolsmission by actively participatingin its cutting-edgeresearch in the lab.

Particpating students included:

Noah Feld, of Woodbridge, Virginia,and a senior in neuroscience who worked in Sontheimers lab withSusan Campbell, a research assistant professor at the Virginia Tech Carilion Research Institute, said he enjoyed the experience of hands-on research. Having the privilege to be constantly immersed in an environment where I was challenged, but also able to learn, gave me a feeling of excitement, as though a new discovery was just around the corner, Feld said.

Amanda Patterson, of Mount Airy, Maryland, and a senior in neuroscience, worked in the laboratory ofGeorgia Hodes, an assistant professor of neuroscience. There, Patterson carried out experiments to understand sex differences involved in stress susceptibility and resilience. The focus of this lab was to determine connections between the immune system and the peripheral nervous system.This fellowship gave me first-hand experience with techniques I didnt even know existed until I was admitted in this program, she said.

Madison ODonnell, of Forest, Virginia,and a senior in neuroscience, worked in the laboratory ofElizabeth Gilbert, an assistant professor in the Department of Animal and Poultry Sciences, part of theCollege of Agriculture and Life Sciences, and an affiliated faculty member of neuroscience. ODonnell contributed to eight experiments on neural control of food intake in chickens and quail, with four experiments being of her own design.

Receiving the fellowship this summer was the greatest success of my undergraduate career and the best experience Virginia Tech has given me, she said. Being able to spend 40-plus hours in the lab every week gave me the opportunity to be taught many lab techniques by my mentors and gain experiences that I would not have gotten anywhere else.

ODonnell expects her summer work to result in two publications, and she plans on pursuing a doctoral degree in cellular and molecular neuroscience at the University of Southern California after she graduates in 2018.

Sontheimer said, We hope to be able to continue this successful program in future summers, providing generations of students a chance to sample the excitement that comes with discovery, which defines the future career path of many of our students.

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Neuroscience marks end of inaugural summer research experience for 18 undergrads - Augusta Free Press

Another Viewpoint: Watch your neck: Physiology and the advent of the smartphone – News Chief

In his 2010 book "I Live in the Future & Here's How It Works," the technology writer Nick Bilton relayed anecdotes about early 19th-century anxieties in Britain at the dawn of train travel.

It was thought that "people would asphyxiate if carried at speeds of more than 20 mph" and reputable scientists believed that traveling at a certain speed "could actually make our bones fall apart." So far, that hasn't happened. While adjusting to the future is often alarming, as Bilton illustrated, humans find a way to cope.

A recent article in the Pittsburgh Post-Gazette drove that point home.

Doctors have identified the condition of "text neck," found most often in teenagers and young adults who stare down at their smartphones for two to four hours a day. An orthopedic surgeon quoted in the article advises people to simply "take a break from that thing." If that proves unrealistic, there's a Pilates class geared for teenagers, which includes a focus on overcoming "text neck." The instructor noticed that four girls in a recent class "could not drop their heads in a relaxed position during the exercises" a clear sign of TN.

It is beyond doubt that the proliferation of digital devices is changing the way people process information: smaller gulps from wider sources, less sustained attention. When you can pry your hands from your own smartphone for a minute, go ahead and wring them over this decline in intellectual capacity.

But the endurance of the human species is testimony to its remarkable ability to adapt. And there's one constant: Each generation is horrified by the decadence of the one following.

The Pittsburgh Post-Gazette

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Watch your neck: Physiology and the advent of the smartphone … – Hawaii Tribune Herald

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Scientists discover potential new improved way to kill cancer cells – Medical Xpress

Scientists at the University of Glasgow have discovered a process to trigger the death of cancer cells that could be more effective than current methods.

The new method of killing cancer cells called Caspase Independent Cell Death (CICD), and published today in Nature Cell Biology, led to the complete eradication of tumours in experimental models.

Currently most anti-cancer therapies (chemotherapy, radiation and immunotherapy) work by killing cancer cells through a process called apoptosis, which activates proteins called caspases, leading to cell death.

But in apoptosis, therapies often fail to kill all cancer cells, leading to disease recurrence, and can also have unwanted side effects that may even promote cancer.

The scientists wanted to develop a way to improve therapy that induces cancer cell killing while also mitigating unwanted toxicity.

Dr Stephen Tait, Cancer Research UK Beatson Institute, Institute of Cancer Sciences, said: "Our research found that triggering Caspase-Independent Cell Death (CICD), but not apoptosis, often led to complete tumour regression.

"Especially under conditions of partial therapeutic response, as our experiments mimic, our data suggests that triggering tumour-specific CICD, rather than apoptosis, may be a more effective way to treat cancer."

Unlike apoptosis, which is a silent form of cell death, when cancer cells die through CICD, they alert the immune system through the release of inflammatory proteins.

The immune system can then attack the remaining tumour cells that evaded initial therapy-induced death.

The researchers used lab-grown colorectal cancer cells to show the advantage of killing cancer cells via CICD, however, these benefits may be applicable to a wide-range of cancer types.

He added: "In essence, this mechanism has the potential to dramatically improve the effectiveness of anticancer therapy and reduce unwanted toxicity. Taking into consideration our findings, we propose that engaging CICD as a means of anti-cancer therapy warrants further investigation."

Dr Justine Alford, Cancer Research UK's senior science information officer, said: "Although many cancer treatments work by triggering apoptosis, that method sometimes fails to finish the job and instead may lead to the tumour becoming harder to treat.

"This new research suggests there could be a better way to kill cancer cells which, as an added bonus, also activates the immune system. Now scientists need to investigate this idea further and, if further studies confirm it is effective, develop ways to trigger this particular route of cell death in humans."

The paper, 'Mitochondrial permeabilization engages NF-kB-dependent anti-tumour activity under caspase deficiency,' is published in Nature Cell Biology.

Explore further: Protein that promotes 'cell-suicide' could revolutionise eye cancer treatment

More information: Evangelos Giampazolias et al. Mitochondrial permeabilization engages NF-B-dependent anti-tumour activity under caspase deficiency, Nature Cell Biology (2017). DOI: 10.1038/ncb3596

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Scientists discover potential new improved way to kill cancer cells - Medical Xpress