Heart attacks can dramatically reshape how the brain functions
Peer-Reviewed Publication
Updates every hour. Last Updated: 8-Jun-2026 05:16 ET (8-Jun-2026 09:16 GMT/UTC)
- A heart attack not only damages the cardiovascular system but can trigger toxic chain reaction linked to depression & anxiety - Identification of methylglyoxal (MG) molecule build up in certain parts of brain following heart attack can be linked to mood and cognition. - Research team has developed a peptide therapeutic that can trap MG to prevent it from damaging cells.
University of Cincinnati College of Medicine structural biologists are the first in the world to visualize a key cell protein as part of recently published research in the journal Cell Reports.
Cells communicate through secreted signaling proteins that regulate metabolism, immunity, development, and tissue repair. But for many of these molecules, scientists still do not know which receptors receive their signals — a long-standing problem that limits both basic biology and drug discovery.
In a review recently published in EXO – Beyond the Cell, researchers from Harvard Medical School present a roadmap for addressing this “orphan receptor” challenge. The study evaluates current deorphanization methods and outlines how next-generation technologies could transform ligand-receptor discovery from a slow, one-at-a-time process into scalable, network-level analysis.To understand birds — their social relationships, their choices, even their feathers — you need to understand the way they see the world.
A new study reveals that many oral cancers are no longer driven by traditional risk factors like smoking or Human papillomavirus infection. Instead, they arise from internal DNA damage and possible microbial influences. By analyzing tumor mutation patterns, researchers identified a distinct subtype of oral squamous cell carcinoma marked by immune evasion and antibacterial responses. These findings reshape our understanding of oral cancer and open the door to more precise, targeted treatments in the future.
Kyoto, Japan -- Like schools of fish and flocks of birds, our cells too can migrate collectively in coordination with their neighbors. This harmonious movement of cells occurs during embryonic development, wound healing, and cancer metastasis. However, since individual cells can only sense limited local information, how they are able to coordinate as a larger collective has remained poorly understood.
Previous studies have demonstrated that this collective migration involves adhesion between cells and waves of ERK signaling activation, named for the ERK proteins involved, and may also be influenced by ZO-1, a scaffolding protein best known for its role in cell-cell adhesion. Building on this knowledge, a team of researchers at Kyoto University was motivated to uncover the elusive mechanism behind collective cell movement.
Using live-cell imaging of Madin-Darby canine kidney cells -- model mammal cells often used in biomedical studies -- the researchers were able to directly observe the movement of cell collectives. They simultaneously monitored ERK activity using a FRET biosensor and visualized ZO-1 localization using fluorescently tagged ZO-1.
Eating is not only about getting enough calories. Animals also need to choose the right nutrients. When the body lacks protein, it must seek essential amino acids — the protein building blocks that cannot be made internally and must come from food.
A research team led by Director SUH Seong-Bae of the Center for Microbiome–Body–Brain Physiology within the Institute for Basic Science (IBS), in collaboration with researchers at Seoul National University and Ewha Womans University, has uncovered how the gut detects protein deficiency and directs the brain to seek out essential nutrients. The study reveals a previously unknown gut-brain signaling system that rapidly alters feeding behavior through coordinated neuronal and hormonal pathways.