Toggle light / dark theme

Your Mother’s Germs May Have Influenced Your Brain’s Development

Our bodies are colonized by a teeming, ever-changing mass of microbes that help power countless biological processes. Now, a new study has identified how these microorganisms get to work shaping the brain before birth.

Researchers at Georgia State University studied newborn mice specifically bred in a germ-free environment to prevent any microbe colonization. Some of these mice were immediately placed with mothers with normal microbiota, which leads to microbes being transferred rapidly.

That gave the study authors a way to pinpoint just how early microbes begin influencing the developing brain. Their focus was on the paraventricular nucleus (PVN), a region of the hypothalamus tied to stress and social behavior, already known to be partly influenced by microbe activity in mice later in life.

Nutrition at the Intersection between Gut Microbiota Eubiosis and Effective Management of Type 2 Diabetes

Nutrition is one of the most influential environmental factors in both taxonomical shifts in gut microbiota as well as in the development of type 2 diabetes mellitus (T2DM). Emerging evidence has shown that the effects of nutrition on both these parameters is not mutually exclusive and that changes in gut microbiota and related metabolites such as short-chain fatty acids (SCFAs) and branched-chain amino acids (BCAAs) may influence systemic inflammation and signaling pathways that contribute to pathophysiological processes associated with T2DM. With this background, our review highlights the effects of macronutrients, carbohydrates, proteins, and lipids, as well as micronutrients, vitamins, and minerals, on T2DM, specifically through their alterations in gut microbiota and the metabolites they produce.

Direct plasma membrane-to-ER lipid transfer outpaces vesicular trafficking, study reveals

Max Planck Institute of Molecular Cell Biology and Genetics led a study showing that directional, non-vesicular lipid transport drives fast, species-selective lipid sorting, outpacing slower, less specific vesicular trafficking, and yielding a quantitative map of retrograde lipid transport in cells.

Thousands of lipid species occupy distinct organelle membranes, with task differences that determine cellular function. Gaps in live-cell imaging capabilities have limited clarity on how individual lipids move between organelles to maintain those tasks.

Biosynthesis of lipids begins in the (ER), followed by distribution toward the and subsequent recycling back into the ER or catabolism in lysosomes, peroxisomes, and mitochondria.

Comprehensive molecular atlas of human hippocampus maps cell subtypes and organization

The hippocampus is an important brain region known to support various cognitive (i.e., mental) processes, including the encoding and retrieval of memories, learning, decision-making and the regulation of emotional states. While extensive research has tried to delineate the structure, functions and organization of the hippocampus, the cell types contained within it and their connections with other neurons have not yet been fully mapped out.

Over the past decades, available methods for studying cell subpopulations, the expressions of genes within them and their connectivity have become increasingly advanced. One of these methods, known as spatially resolved transcriptomics, works by measuring the expression of genes in cells while preserving their arrangement in space. Another called single-nucleus RNA-sequencing (snRNA-seq), allows scientists to examine RNA molecules inside individual cell nuclei to detect differences between them and categorize cells into different subtypes.

Researchers at Johns Hopkins Bloomberg School of Public Health, the Lieber Institute for Brain Development and Johns Hopkins School of Medicine recently used a combination of these two experimental techniques to examine cells in tissue extracted from the hippocampus. Their paper, published in Nature Neuroscience, introduces a comprehensive molecular atlas of the hippocampus that maps different cell subtypes and their organization.

Depression linked to presence of immune cells in the brain’s protective layer

Immune cells released from bone marrow in the skull in response to chronic stress and adversity could play a key role in symptoms of depression and anxiety, say researchers.

The discovery—found in a study in mice—sheds light on the role that inflammation can play in mood disorders and could help in the search for new treatments, in particular for those individuals for whom current treatments are ineffective.

Around 1 billion people will be diagnosed with a mood disorder such as or anxiety at some point in their life. While there may be many underlying causes, —when the body’s immune system stays active for a long time, even when there is no infection or injury to fight—has been linked to depression. This suggests that the immune system may play an important role in the development of mood disorders.

Exploring criminal behavior in patients with dementia

A suspected perpetrator who can barely remember his name, several traffic violations committed by a woman in her mid-fifties who is completely unreasonable and doesn’t understand her behavior—should such cases be brought before a court? And how does the state deal with people who commit acts of violence without meaning to?

Those questions come to mind if one hears those examples from everyday clinical praxis with persons suffering from . Neurodegenerative diseases might affect several functions of the brain, ranging from memory in Alzheimer’s disease to behavior, such as in behavioral variant frontotemporal dementia, and to sensorimotor function in Parkinson’s disease.

One of the most interesting consequences of these alterations is the fact that persons affected by these diseases might develop criminal risk behavior like harassment, traffic violation, theft or even behavior causing harm to other people or animals, even as the first disease sign.

CRISPR’s efficiency triples in lab tests with DNA-wrapped nanoparticles

With the power to rewrite the genetic code underlying countless diseases, CRISPR holds immense promise to revolutionize medicine. But until scientists can deliver its gene-editing machinery safely and efficiently into relevant cells and tissues, that promise will remain out of reach.

Now, Northwestern University chemists have unveiled a new type of nanostructure that dramatically improves CRISPR delivery and potentially extends its scope of utility.

Called lipid nanoparticle spherical nucleic acids (LNP-SNAs), these tiny structures carry the full set of CRISPR editing tools—Cas9 enzymes, guide RNA and a DNA repair template—wrapped in a dense, protective shell of DNA. Not only does this DNA coating shield its cargo, but it also dictates which organs and tissues the LNP-SNAs travel to and makes it easier for them to enter cells.

Antifungal Drug Resistance: An Emergent Health Threat

Fungal infections, named mycosis, can cause severe invasive and systemic diseases that can even lead to death. In recent years, epidemiological data have recorded an increase in cases of severe fungal infections, caused mainly by a growing number of immunocompromised patients and the emergence of fungal pathogenic forms that are increasingly resistant to antimycotic drug treatments. Consequently, an increase in the incidence of mortality due to fungal infections has also been observed. Among the most drug-resistant fungal forms are those belonging to the Candida and Aspergillus spp. Some pathogens are widespread globally, while others are endemic in some areas only. In addition, some others may represent a health threat for some specific subpopulations and not for the general public. In contrast to the extensive therapeutic armamentarium available for the antimicrobial chemotherapeutic treatment of bacteria, for fungal infections there are only a few classes of antimycotic drugs on the market, such as polyenes, azoles, echinocandins, and a few molecules are under trial. In this review, we focused on the systemic mycosis, highlighted the antifungal drug compounds available in the pipeline, and analyzed the main molecular mechanisms for the development of antifungal resistance to give a comprehensive overview and increase awareness on this growing health threat.

How B-cell receptor types shape lymphoma cell survival and growth

A Northwestern Medicine study has uncovered new insights that may aid in understanding and potentially treating one of the most common and aggressive forms of non-Hodgkin lymphoma, according to findings published in Science Advances.

The study described critical differences in B-cell receptor (BCR) types that may influence the progression and treatment of diffuse large B-cell and other forms of B-cell leukemia and lymphomas, which affect more than 80,000 Americans each year.

“B-cells, which are responsible for producing antibodies, rely on BCRs for survival and growth. While most research has focused on the IgM variant of BCRs, this study sheds light on the lesser-understood IgG1 variant,” said Vipul Shukla, Ph.D., assistant professor of Cell and Developmental Biology, who was co-senior author of the study.

/* */