Detecting diabetes among people at risk

When diabetes starts to develop but no symptoms are yet detectable, part of the beta cells of the pancreas (in green) disappear (right image) compared to a healthy individual (left image). This previously undetectable decrease could be identified by measuring the level of 1,5-anhydroglucitol in the blood.
Credit: UNIGE - Laboratory of Prof. Pierre Maechler

A team from the UNIGE in collaboration with the HUG has discovered a molecule that can identify the development of diabetes before the first symptoms appear.

Diabetes is a severe and growing metabolic disorder. It already affects hundreds of thousands of people in Switzerland. A sedentary lifestyle and an excessively rich diet damage the beta cells of the pancreas, promoting the onset of this disease. If detected early enough, its progression could be reversed, but diagnostic tools that allow for early detection are lacking. A team from the University of Geneva (UNIGE) in collaboration with several other scientists, including teams from the HUG, has discovered that a low level of the sugar 1,5-anhydroglucitol in the blood is a sign of a loss in functional beta cells. This molecule, easily identified by a blood test, could be used to identify the development of diabetes in people at risk, before the situation becomes irreversible. These results can be found in the Journal of Clinical Endocrinology & Metabolism.

In Switzerland, almost 500,000 people suffer from diabetes. This serious metabolic disorder is constantly increasing due to the combined effect of a lack of physical activity and an unbalanced diet. If detected early enough at the pre-diabetes stage, progression to an established diabetes can be counteracted by adopting an appropriate lifestyle. Unfortunately, one third of patients already have cardiovascular, renal or neuronal complications at the time of diagnosis, which impacts their life expectancy.

Scientists develop gel made from spider silk proteins for biomedical applications

The hydrogels stained with a fluorescent dye that binds to amyloid structures and the corresponding brightfield image.
Microscope photo credit: Tina Arndt.

Researchers at KI and SLU have discovered that spider silk proteins can be fused to biologically active proteins and be converted into a gel at body temperature. One of the goals is to develop an injectable protein solution that forms a gel inside the body, which could be used in tissue engineering and for drug release, but also make gels that can streamline chemical processes where enzymes are used. The study is published in Nature Communications.

“We have developed a completely new method for creating a three-dimensional gel from spider silk that can be designed to deliver different functional proteins,” says Anna Rising, research group leader at the Department of Biosciences and Nutrition, Karolinska Institutet (KI) and professor at the Department of Anatomy, Physiology and Biochemistry, Swedish University of Agricultural Sciences (SLU). “The proteins in the gel are very close together and the method is so mild that it can be used even for sensitive proteins.”

Supernova remnant is source of extreme cosmic particles

Astronomers have long sought the launch sites for some of the highest energy protons in our galaxy. Now, a study using 12 years of data from NASA’s Fermi Gamma-ray Space Telescope confirms that a remnant of a supernova, or star explosion, is just such a place, solving a decade-long cosmic mystery.

Previously, Fermi has shown that the shock waves of exploded stars boost particles to speeds comparable to that of light. Called cosmic rays, these particles mostly take the form of protons, but can include atomic nuclei and electrons. Because they all carry an electric charge, their paths become scrambled as they whisk through our galaxy’s magnetic field, which masks their origins. But when these particles collide with interstellar gas near the supernova remnant, they produce a telltale glow in gamma rays—the highest-energy light there is.

“Theorists think the highest-energy cosmic ray protons in the Milky Way reach a million billion electron volts, or PeV (for peta-electron-volt) energies,” says Ke Fang, an assistant professor of physics at the University of Wisconsin–Madison’s Wisconsin IceCube Particle Astrophysics Center. “The precise nature of their sources, which we call PeVatrons, has been difficult to pin down.”

MIT team reports giant response of semiconductors to light

MIT graduate student Jiahao Dong with the nanoindentation machine used in recent MIT work on the response of semiconductors to light.
Credits: Elizabeth Thomson/Materials Research Laboratory

In an example of the adage “everything old is new again,” MIT engineers report a new discovery in semiconductors, well-known materials that have been the focus of intense study for over 100 years thanks to their many applications in electronic devices.

The team found that these important materials not only become much stiffer in response to light, but the effect is reversible when the light is turned off. The engineers also explain what is happening at the atomic scale, and show how the effect can be tuned by making the materials in a certain way — introducing specific defects — and using different colors and intensities of light.

“We’re excited about these results because we’ve uncovered a new scientific direction in an otherwise very well-trod field. In addition, we found that the phenomenon may be present in many other compounds,” says Rafael Jaramillo, the Thomas Lord Associate Professor of Materials Science and Engineering at MIT and leader of the team.

Says Ju Li, another MIT professor involved in the work, "to see defects having such big effects on elastic response is very surprising, which opens the door to a variety of applications. Computation could help us screen many more such materials." Li is the Battelle Energy Alliance Professor in Nuclear Science and Engineering (NSE) with a joint appointment in the Department of Materials Science and Engineering (DMSE). Both Jaramillo and Li are also affiliated with the Materials Research Laboratory.

Thirdhand Smoke Exposures Surpass Health Risk Guideline Levels

Cigarettes and other tobacco products produce chemicals that linger in indoor environments, putting all other occupants in harm’s way. Credit: Gerd Altmann from Pixabay

Some smells seem to seep into everything they touch. Tobacco smoke is one of the worst offenders.

Thirdhand smoke refers to residual nicotine and other hazardous chemicals that contaminate the indoor environment after smoking. Think of the lingering smell you’ve probably encountered when handling the clothes of a person who smokes a pack a day, or when checking into a tidy but cigarette-friendly hotel room.

Scientists at the U.S. Department of Energy’s Lawrence Berkeley National Laboratory (Berkeley Lab) first identified thirdhand smoke as a potential health hazard a decade ago. Their newest study develops more quantitative insights into its long-term health risks. They found that concentrations of toxic chemicals lingering in indoor environments where cigarettes have been smoked can exceed risk guidelines from the State of California, meaning that non-smokers can be exposed to health risks by living in contaminated spaces.

The study was published in the journal Environmental Science & Technology. Alongside Berkeley Lab scientists, co-authors on this work include collaborators from UC San Francisco, UC Riverside, and San Diego State University. These teams are members of the California Consortium on Thirdhand Smoke, funded by the Tobacco-Related Disease Research Program, which is managed by the University of California.

Berkeley Lab’s researchers previously discovered that aerosolized nicotine, released during smoking and vaping, adsorbs to indoor surfaces, where it can interact with a compound present in indoor air called nitrous acid (HONO) to form strongly carcinogenic compounds called tobacco-specific nitrosamines (TSNAs). Accumulated nicotine on household surfaces can continuously generate TSNAs, long after smoke clears the room.

Researchers identify a hormone from fat cells that restrains tumor growth in mice

Normal liver tissue (top) and a liver cancer nodule (bottom) containing many dividing cells (labeled in green). Red indicates blood vessels.
Photo credit: Jiandie Lin, Ph.D., University of Michigan Life Sciences Institute

A hormone secreted by fat cells can restrain the growth of liver tumors in mice, according to a new study from the University of Michigan Life Sciences Institute.

The findings offer proof-of-concept for developing therapies against hepatocellular carcinoma, the most common form of liver cancer.

Jiandie Lin and his team use mice as a model to study how molecular and cellular changes are affected by nonalcoholic fatty liver disease, and how these changes consequently lead to the progression of this disease. While it begins as a relatively benign accumulation of fat in the liver, the disorder can develop into nonalcoholic steatohepatitis, or NASH, which increases the risk for liver cancer.

The liver contains scores of different cell types, including various immune cells. Using single-cell RNA sequencing, a technology for probing gene expression of individual cells within complex tissues, Lin and his team previously constructed a liver cell atlas and a blueprint of intercellular signaling in healthy and NASH mouse livers.

For this latest study, scheduled to be published Aug. 15 in Cell Metabolism, the scientists wanted to identify specific molecular changes in the NASH state that disrupt balance and interactions of these cell types, as potential therapeutic targets to reverse the progression from NASH to cancer.

Weird and wonderful world of fungi shaped by evolutionary bursts

Fungi
Scientific Frontline Fungi Gallery
Credit: Heidi-Ann Fourkiller

Scientists at the University of Bristol have discovered that the vast anatomical variety of fungi stems from evolutionary increases in multicellular complexity.

Most people recognize that fungi come in an assortment of shapes and sizes. However, these differences, often referred to as the disparity of a group, had never been analyzed collectively.

Researcher Thomas Smith, who conducted the study while at Bristol’s School of Earth Sciences, explained: “Prior to our analyses, we didn’t know how this variety was distributed across the different types of fungi. Which groups are the most varied when considering all parts of the fungal body plan? Which are the least? How has this variety accumulated and diminished through time? What has shaped these patterns in disparity? These are the questions we sought to answer.”

What they found was that fungal disparity has evolved episodically through time, and that the evolution of multicellularity in different fungi appears to open the door for greater morphological variety. They saw increases in disparity associated with both the emergence of the first multicellular fungi, and then the evolution of complex fruiting bodies such as mushrooms and saddles in dikaryotic species. These fungi are defined by the inclusion of a dikaryon, a cell with two separate nuclei, in their life cycles.

Underwater Snow Gives Clues About Europa’s Icy Shell

An illustration of NASA’s Europa Clipper spacecraft flying by Jupiter’s moon Europa. The spacecraft, which is planned to launch in 2024, will carry an ice-penetrating radar instrument developed by scientists at the University of Texas Institute for Geophysics.
Credit: NASA/JPL-Caltech.

Below Europa’s thick icy crust is a massive, global ocean where the snow floats upwards onto inverted ice peaks and submerged ravines. The bizarre underwater snow is known to occur below ice shelves on Earth, but a new study shows that the same is likely true for Jupiter’s moon, where it may play a role in building its ice shell.

The underwater snow is much purer than other kinds of ice, which means Europa’s ice shell could be much less salty than previously thought. That’s important for mission scientists preparing NASA’s Europa Clipper spacecraft, which will use radar to peek beneath the ice shell to see if Europa’s ocean could be hospitable to life. The new information will be critical because salt trapped in the ice can affect what and how deep the radar will see into the ice shell, so being able to predict what the ice is made of will help scientists make sense of the data.

The study, published in the August edition of the journal Astrobiology, was led by The University of Texas at Austin, which is also leading the development of Europa Clipper’s ice penetrating radar instrument. Knowing what kind of ice Europa’s shell is made of will also help decipher the salinity and habitability of its ocean.

“When we’re exploring Europa, we’re interested in the salinity and composition of the ocean, because that’s one of the things that will govern its potential habitability or even the type of life that might live there,” said the study’s lead author Natalie Wolfenbarger, a graduate student researcher at the University of Texas Institute for Geophysics (UTIG) in the UT Jackson School of Geosciences.

Northernmost Neolithic Fortifications Found

The group of archaeologists in the project under the state order of the Ministry of Science and Education of Russia is headed by Victor Borzunov.
Photo from Victor Borzunov's personal archive

To establish and characterize in detail the livelihood strategies of the primitive population of the Trans-Urals and Western Siberia of the Stone, Bronze and Early Iron eras. This is the task archeologists at Ural Federal University have set for themselves within the interdisciplinary project "Regional Identity of Russia: Comparative Historical and Philological Studies". Scientists have found that during the New Stone Age, the aborigines of the forest belt of the north of the Eurasian continent continued to maintain an appropriate economy and could not rise to the level of a fundamentally new production economy.

Scientists conduct research in this area under the state order of the Ministry of Science and Education of Russia (№ FEUZ-2020-0056) and under a grant from the Russian Science Foundation. The group in the project is headed by Victor Borzunov, a Senior Researcher of the Fundamental Research Archaeological Laboratory of UrFU.

The work, which continued many years of research by the laboratory personnel, is carried out in three main directions. The first is the study of neolithization of the societies of the Ural-West Siberian Region. In other words, the peculiarities of ancient groups of 6th-4th millennia B.C. to the advanced innovations of the Old World, such as productive economy, more or less strong sedentary life, large stationary settlements, ceramic production, defense architecture, fundamentally different house-building, stone processing, new social structures etc.

The second direction is the analysis of the origin and development of the ancient defensive architecture of the north of Eurasia in the 7th millennium B.C. - 3rd century A.D., its place and role in the general system of origin and development of fortified settlements, proto-cities and cities of the Old World.

Road signs for immune defense cells

The mechanism of MHC I assembly, epitope editing and quality control within the peptide loading complex (PLC). The fully assembled PLC machinery of antigen processing is formed by the antigen transport complex TAP1/2, the chaperones calreticulin, ERp57, and tapasin, and the heterodimeric MHC I (heavy and light chain in teal and green, respectively).
Credit: Christoph Thomas & Robert Tampé

How do killer T cells recognize cells in the body that have been infected by viruses? Matter foreign to the body is presented on the surface of these cells as antigens that act as a kind of road sign. A network of accessory proteins – the chaperones – ensure that this sign retains its stability over time. Researchers at Goethe University have now reached a comprehensive understanding of this essential cellular quality control process. Their account of the structural and mechanistic basis of chaperone networks has just appeared in the prestigious science journal Nature Communications. These new findings could be harbingers of progress in areas such as vaccine development.

Organisms are constantly invaded by pathogens such as viruses. Our immune system swings into action to combat these pathogens immediately. The innate non-specific immune response is triggered first, and the adaptive or acquired immune response follows. In this second defense reaction, specialized cytotoxic T lymphocytes known as killer T cells destroy cells in the body that have been infected and thus prevent damage from spreading. Humans possess a repertoire of some 20 million T cell clones with varying specificity to counter the multitude of infectious agents that exist. But how do the killer T cells know where danger is coming from? How do they recognize that something is wrong inside a cell in which viruses are lurking? They can't just have a quick peek inside.