After a decade of obscurity, the technology is being used to track people’s movements.
Over a decade ago, Neal Patwari lay in a hospital bed, carefully timing his breathing.
Researchers ingeniously repurposed DNA to assemble a miniaturized blaster at the molecular level.
Summary: Researchers have developed the first stem cell culture method that accurately models the early stages of the human central nervous system (CNS), marking a significant breakthrough in neuroscience. This 3D human organoid system simulates the development of the brain and spinal cord, offering new possibilities for studying human brain development and diseases.
By using patient-derived stem cells, the model can potentially lead to personalized treatment strategies for neurological and neuropsychiatric disorders. The innovation opens new doors for understanding the intricacies of the human CNS and its disorders, surpassing the capabilities of previous models.
A relatively new way to attack cancer, called immunotherapy, is revolutionizing cancer treatment by enabling patients’ own immune systems to attack cancer cells. It hasn’t worked for many kinds of cancers, though — evading the immune system is one of the first tricks that cancer learns. As it turns out, many cancers are also pretty good at hiding from immunotherapies.
In a recent study published in the journal Science, though, Salk Institute researchers have discovered a new way to make cancer visible to immunotherapy. To do this, the team reprogrammed mitochondria — the organelle widely memed as the “powerhouse of the cell” — to make cancer cells easier to find and kill.
The engine of cancer: What connects mitochondria and cancers? Another hallmark of cancer is their uncontrolled growth. Fueling this rapid and relentless proliferation requires a lot of energy. This increased demand is met by changes in how mitochondria function in cancer cells.
Dr. John Swierk: “This is also the first study to explicitly look at inks sold in the United States and is probably the most comprehensive because it looks at the pigments, which nominally stay in the skin, and the carrier package, which is what the pigment is suspended in.”
Do the ingredients in tattoo inks match the labels on their respective bottles? This is what a recent study published in Analytical Chemistry hopes to address as a team of researchers from Binghamton University investigated the accuracy of ink ingredients and what’s labeled on their containers. This study holds the potential to help scientists, artists, and their customers better understand the health risks, to include allergic reactions and other risks, of using the wrong ink ingredients for tattoos.
For the study, the researchers examined ingredients from 54 inks emanating from nine common brands within the United States with the goal of ascertaining their exact chemical compositions compared to what was labeled on their respective bottles. In the end, the researchers identified that 45 of the 54 inks possessed a myriad of pigments and/or additives that were not properly labeled on the bottles that could pose health risks to customers receiving ink tattoos, including allergic skin reactions and other long-term health risks, including non-skin-related risks, such as cancer. Despite the alarming findings, the researchers could not ascertain which unlisted ingredients were intentionally or accidentally added to the inks.
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The speed of innovation in bioelectronics and critical sensors gets a new boost with the unveiling of a simple, time-saving technique for the fast prototyping of devices.
A research team at KTH Royal Institute of Technology and Stockholm University reported a simple way to fabricate electrochemical transistors using a standard Nanoscribe 3D micro printer. Without cleanroom environments, solvents, or chemicals, the researchers demonstrated that 3D micro printers could be hacked to laser print and micropattern semiconducting, conducting, and insulating polymers.
Anna Herland, professor in Micro-and Nanosystems at KTH, says the printing of these polymers is a key step in prototyping new kinds of electrochemical transistors for medical implants, wearable electronics and biosensors.
A new study from a team of McGill University and Vanderbilt University researchers is shedding light on our understanding of the molecular origins of some forms of autism and intellectual disability.
For the first time, researchers were able to successfully capture atomic resolution images of the fast-moving ionotropic glutamate receptor (iGluR) as it transports calcium. iGluRs and their ability to transport calcium are vitally important for many brain functions such as vision or other information coming from sensory organs. Calcium also brings about changes in the signaling capacity of iGluRs and nerve connections, which are key cellular events that lead to our ability to learn new skills and form memories.
IGluRs are also key players in brain development and their dysfunction through genetic mutations has been shown to give rise to some forms of autism and intellectual disability. However, basic questions about how iGluRs trigger biochemical changes in the brain’s physiology by transporting calcium have remained poorly understood.
A new technique for electrospinning sponges has allowed scientists from the University of Surrey to directly produce 3D scaffolds—on which skin grafts could be grown from the patient’s own skin.
Electrospinning is a technique that electrifies droplets of liquid to form fibers from plastics. Previously, scientists had only been able to make 2D films. This is the first time anybody has electro-spun a 3D structure directly and on-demand so that it can be produced to scale. The research is published in the journal Nanomaterials.
Chloe Howard, from Surrey’s School of Computer Science and Electronic Engineering, said, After spinning these scaffolds, we grew skin cells on them. Seven days later, they were twice as viable as cells grown on 2D films or mats. They even did better than cells grown on plasma-treated polystyrene—previously, the gold standard. They were very happy cells on our 3D scaffolds.
Networks can represent changing systems, like the spread of an epidemic or the growth of groups in a population of people. But the structure of these networks can change, too, as links appear or vanish over time. To better understand these changes, researchers often study a series of static “snapshots” that capture the structure of the network during a short duration.
Network theorists have sought ways to combine these snapshots. In a new paper in Physical Review Letters, a trio of SFI-affiliated researchers describe a novel way to aggregate static snapshots into smaller clusters of networks while still preserving the dynamic nature of the system. Their method, inspired by an idea from quantum mechanics, involves testing successive pairs of network snapshots to find those for which a combination would result in the smallest effect on the dynamics of the system—and then combining them.
Importantly, it can determine how to simplify the history of the network’s structure as much as possible while maintaining accuracy. The math behind the method is fairly simple, says lead author Andrea Allen, now a data scientist at Children’s Hospital of Philadelphia.
Researchers report in the journal Cell that ancient viruses may be to thank for myelin—and, by extension, our large, complex brains.
The team found that a retrovirus-derived genetic element or “retrotransposon” is essential for myelin production in mammals, amphibians, and fish. The gene sequence, which they dubbed “RetroMyelin,” is likely a result of ancient viral infection, and comparisons of RetroMyelin in mammals, amphibians, and fish suggest that retroviral infection and genome-invasion events occurred separately in each of these groups.
“Retroviruses were required for vertebrate evolution to take off,” says senior author and neuroscientist Robin Franklin of Altos Labs-Cambridge Institute of Science. “If we didn’t have retroviruses sticking their sequences into the vertebrate genome, then myelination wouldn’t have happened, and without myelination, the whole diversity of vertebrates as we know it would never have happened.”
