Lifeboat Foundation

University of Copenhagen researchers have invented a “quantum drum” that can measure pressure, a gas leak, heat, magnetism and a host of other things with extreme precision. It can even scan the shape of a single virus. The invention has now been adapted to work at room temperature and may be finding its way into our phones.

Humans have tried to measure the world around them since ancient times. Now, researchers are using the laws of quantum physics to develop one of the most sensitive measuring devices the world has ever seen. One day, it may even be yours. With two innovative solutions, researchers at the Niels Bohr Institute have found a way to get quantum technology into our pockets.

The heart of the apparatus could be called a “quantum drum”: It is a thin membrane that vibrates like a drum skin, but with so small an amplitude that the laws of quantum physics are needed to describe what’s happening. In other words, it’s vibrating really fast. This means the drum can be used as an ultra-precise measuring device—a quantum supersensor.

A team of nearly 100 scientists recently mapped the cell-type taxonomy in the macaque cortex and revealed the relationship between cell-type composition and various primate brain regions by using the self-developed spatial transcriptome sequencing technology Stereo-seq and snRNA-seq technology, which provides a molecular and cellular basis for further investigation into neural circuits.

The study was published in Cell.

Primates have a vast number of neurons that form complex and intricate neural circuits supporting advanced cognition and behavior. Disruptions in these cells and circuits can lead to various brain disorders. Understanding the composition and spatial distribution of cells in the brain, as well as the relationships between them, is a fundamental question in neuroscience, comparable to the periodic table in chemistry, the world map in geographic discoveries, or the DNA base sequence discovered through human genome sequencing.

To enjoy the scent of morning coffee and freshly baked cookies or to perceive the warning smell of something burning, the brain needs two types of cells, neurons and astrocytes, to work closely with each other. Research has shown a great deal of the changes that occur in neurons during olfactory, or smell, perception, but what are the astrocyte responses and how they contribute to the sensory experience remains unclear.

Researchers at Baylor College of Medicine and collaborating institutions report in the journal Science the responses of astrocytes to olfactory stimulation, revealing a new mechanism that is required to maintain astrocyte-neuron communication and process olfactory sensation.

“Previous studies have shown that under natural conditions in a living animal, olfactory stimulation of the brain activates neurons first, which changes the genes these neurons express to be able to mediate the olfactory sensation,” said first author Dr. Debosmita Sardar, a postdoctoral associate in Dr. Benjamin Deneen’s lab at Baylor. “In this study, we investigated what occurred to astrocytes following neural activity during olfactory stimulation and uncovered changes that had not been described before.”

The immune system is an incredibly complex network that has some amazing capabilities. It can eliminate dangerous cells that may lead to cancer, and defend the body against a wide variety of pathogenic invaders. It also has the ability to remember those encounters with pathogens so if they happen again, the immune system is primed to respond more quickly and forcefully against the offender. Scientists have now learned more about how the immune system memory is created at the molecular level. The findings have been reported in Science Immunology.

When immune cells are exposed to an invader, they can recognize structures called antigens on the surface of the pathogen. In this study, the researchers compared immune cells that had never been exposed to an antigen, so-called naive cells, to immune cells that had been in contact with an antigen, known as memory cells. The investigators wanted to identify the epigenetic differences between these cell types, which are changes in DNA that can impact gene expression, such as structural shifts or chemical tags, but do not alter the sequence of the genome. Epigenetic changes might explain why memory cells can react so quickly while naive cells are comparatively slow.

Consider it a technological solution to the problem of death.

Over the last couple years, I’ve been writing about creating ghosts — perhaps an inevitability in the midst of a pandemic.

Artur Sychov, founder and CEO of metaverse company Somnium Space, has joined the quest against loss. Using motion capture and voice data, he wants to create duplicate avatars that can move as you moved and speak as you spoke, using your voice.

Marion Patten sadly passed away two years after her ovarian cancer diagnosis. Today, her husband Wayne finds happiness in supporting research that helps other women like Marion.

For a long time, neuroscientists believed that the neurons you are born with are the neurons you have for the rest of your life, and any neuron lost will not be replaced. Recent research has shown that specific brain regions contain neural stem cells that can generate new neurons. In this talk, Dr Daniel Berg of the University of Aberdeen will discuss what we know about these stem cells and what we can do to activate them to generate more neurons.

Watch this presentation on LabRoots at: http://www.labroots.com/webcast/keynote-speaker-regulation-a…ippocampus.

In the adult central nervous system (CNS) small populations of neurons are formed in the adult olfactory bulb and dentate gyrus of the hippocampus. In the adult hippocampus, newly born neurons originate from stem cells that exist in the subgranular zone of the dentate gyrus. Progeny of these putative stem cells differentiate into neurons in the granular layer within a month of the cells’ birth, and this late neurogenesis continues throughout the adult life of all mammals. Environmental stimulation can differentially effect the proliferation, migration and differentiation of these cells in vivo. These environmentally induced changes in the structural organization of the hippocampus, result in changes in electrophysiological responses in the hippocampus, as well as in hippocampal related behaviors. We are studying the cellular, molecular, as well as environmental influences that regulate neurogenesis in the adult brain. We have recently identified several molecules that work coordinately to regulate proliferation, survival and differentiation of these adult derived stem cells. In addition, we have demonstrated that specific types of activity can influence the behavior of these newly born cells. Finally, we have developed several methods to monitor the in vivo maturation of neurogenesis in vivo, which has provided insight to the functional importance of neurogenesis to behavior. A consensus model of the function of adult neurogenesis is emerging.

According to new research, butterflies and moths share “blocks” of DNA that are more than 200 million years old. Scientists from the Universities of Exeter (UK), Lübeck (Germany) and Iwate (Japan) devised a tool to compare the chromosomes (DNA molecules) of different butterflies and moths.

They found blocks of chromosomes that exist in all moth and butterfly species, and also in Trichoptera – aquatic caddisflies that shared a common ancestor with moths and butterflies some 230 million years ago. Moths and butterflies (collectively called Lepidoptera) have widely varying numbers of chromosomes – from 30 to 300 – but the study’s findings show remarkable evidence of shared blocks of homology (similar structure) going back through time.

“DNA is compacted into individual particles or chromosomes that form the basic units of inheritance,” said Professor Richard ffrench-Constant, from the Centre for Ecology and Conservation on Exeter’s Penryn Campus in Cornwall. “If genes are on the same ‘string’, or chromosome, they tend to be inherited together and are therefore ‘linked’.