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New postnatal gene therapy offers hope for congenital hearing loss

Hereditary hearing loss affects millions globally, with mutations in the SLC26A4 gene among the most common genetic triggers, particularly across Asian populations. This condition leads to severe-to-profound deafness accompanied by inner ear malformations, such as an abnormally enlarged vestibular aqueduct and endolymphatic sac.

While gene replacement therapies have long held immense potential, experimental interventions have historically been restricted to the embryonic stage. Delivering genetic material before birth presents steep ethical and practical hurdles, creating a critical roadblock for real-world medical applications.

Brain aneurysm map reveals cell types tied to rupture risk

A new study from UC San Francisco shows how certain cells in the brain may cause aneurysms to weaken and rupture. It helps explain why some aneurysms burst while others do not and could lead to new ways of predicting and possibly preventing strokes.

Brain aneurysms are bulges in blood vessels that can go unnoticed for years. If they rupture, they can cause a severe and often deadly type of stroke. About one in 50 Americans has a brain aneurysm, but doctors still struggle to predict which ones are most dangerous.

The new study helps to unpack the biology behind these events by mapping the cells in artery walls and the interactions that weaken them.

Gold-laced nanoparticles could eventually spot and treat endometriosis without surgery

Endometriosis is a painful, common condition affecting women worldwide, but treatment and diagnosis options are scarce. A new University of Mississippi-led study may have found an answer to both problems.

Early results from a study published in Communications Chemistry show that gold-laced nanoparticles can hitchhike on white blood cells. By using those cells as a delivery vehicle, the team hopes to identify and treat endometriosis without repeated surgeries.

“Lots of women go through their lives being in enormous amounts of pain and thinking that it’s normal, and it’s not normal,” said Eden Tanner, assistant professor of chemistry and biochemistry, who authored the study with a team of Ole Miss researchers.

Fish-inspired sensor tracks how human heart tissue responds to disease and treatment

Engineers have developed a new way to monitor how tiny lab-grown human heart tissues beat—by effectively “listening” to the ripples they create. The team has created a wireless, noninvasive sensing platform that can biomechanically measure how strongly the miniature heart tissues, known as cardiac organoids, beat in real time. The research could help accelerate drug development, improve disease modeling and reduce reliance on animal testing, offering a more human-relevant way to study how the heart works.

Cardiac organoids are 3D clusters of human heart cells grown in a laboratory that are used to evaluate the safety and efficacy of new drugs prior to clinical trials, as well as study disease. While they don’t replicate the full structure of a human heart, they mimic key behaviors, especially how heart muscles contract when drugs are administered.

They are increasingly seen as a powerful alternative to animal models, which often fail to fully capture how human biology works.

Atherosclerosis Profiling Reveals BHLHE40 as a Candidate Modulator of VSMC

BACKGROUND: Vascular smooth muscle cells (VSMCs) play a central role in atherosclerosis by undergoing phenotypic modulation from a quiescent, contractile state to a range of synthetic phenotypes, including fibroblast-like, macrophage-like, and lipid-laden foam cell–like states. However, a comprehensive multimodal characterization and understanding of the transcriptional programs driving these transitions remain incomplete. METHODS: To comprehensively define the phenotypic diversity of VSMCs during atherosclerosis progression, we performed in-depth profiling using cellular indexing of transcriptomes and epitopes by sequencing and bulk RNA sequencing in a VSMC-lineage–tracing atherosclerotic mouse model. Insights from these data sets guided the design of targeted in vitro experiments to investigate candidate regulatory mechanisms.

Plasma and graphene combine to protect metal surfaces from corrosion

Plasma is an ionized gas, often referred to as the fourth state of matter. Plasmas, which are created artificially by applying energy to a gas, are found in the fluorescent tubes that illuminate kitchens. However, they have many other possible applications, such as the production of graphene.

The Plasma Innovation Laboratory (LIPs) at the University of Córdoba has already made progress in using plasma to produce graphene, the revolutionary material that earned its discoverers the Nobel Prize. Recently, a new technological design boosted graphene production by more than 22%. Continuing along this line of research, the team is now proposing two methods for applying graphene—also highly anticorrosive—to metal surfaces using microwave plasmas at atmospheric pressure, with the aim of not altering the properties of the metals.

The research is published in the journal Surfaces and Interfaces.

Rethinking mRNA vaccines: Liver targeting can suppress immunity, while muscle boosts it

A new study by researchers at the Icahn School of Medicine at Mount Sinai overturns a longstanding assumption about how mRNA vaccines generate immunity, revealing that certain non-immune cells help determine vaccine effectiveness.

The study, published in Nature Biotechnology, also introduces a powerful and versatile technology to control the expression of mRNA drugs, which the researchers demonstrate can enhance the effectiveness of mRNA cancer vaccines in preclinical studies of lymphoma. The paper is titled “mRNA vaccine immunity is enhanced by hepatocyte detargeting and not dependent on dendritic cell expression.”

The findings provide a new framework for designing mRNA vaccines and mRNA therapeutics, with immediate implications for cancer immunotherapy, infectious disease vaccines, and gene-editing treatments.

Molecular mechanics behind heart cell restructuring revealed

Microtubules, part of heart muscle cells’ internal “skeleton,” help determine how the heart changes shape under stress, and a common signaling pathway called the ERK pathway acts as a key controller of where the building materials for these cells’ growth are delivered inside them, a pair of new studies show. These findings, from a team at the Perelman School of Medicine at the University of Pennsylvania, point to possible new ways to address harmful heart remodeling that can be linked to heart failure.

“The molecular decision behind how a heart cell, and by extension the heart, changes in size and shape has been a mystery, even though we’ve known that heart cells do change in length and width over a person’s life in response to different conditions,” said the studies’ senior author Benjamin Prosser, Ph.D., a professor of Physiology.

“But now that we know what is doing the work and what guides it, that opens the door to targeting these mechanisms and correcting abnormal growth.”

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