HEALTH
Brain's Battle: How Tiny Bubbles and Cells Team Up to Cause Stroke Damage
Tue Feb 25 2025
Macrophages are like the body's cleanup crew. They rush to the scene of a stroke to help. But sometimes, they make things worse. They release tiny bubbles called exosomes that can mess with the brain's blood vessels. This is part of what happens in a condition called cerebral ischemia-reperfusion injury, or CIRI. It's like when you twist a hose and then let go. The water flow can cause damage.
Scientists have been trying to figure out how these exosomes work. They found a special molecule called THBS1. It's like a troublemaker that can cause more damage. In a stroke, THBS1 levels go up in these exosomes. It's found in the blood of stroke patients and in the brains of mice that have had a stroke.
THBS1 causes problems by messing with a process called ferroptosis. This is a type of cell death that can damage the brain's blood vessels. Scientists found that THBS1 binds to a protein called OTUD5. This leads to another protein, GPX4, being broken down. This breakdown is what causes ferroptosis.
But there's hope. Scientists found a compound called salvianolic acid B, or SAB. It can stop THBS1 from causing trouble. SAB can stop THBS1 from binding to OTUD5. This means GPX4 isn't broken down, and ferroptosis doesn't happen.
The brain is a complex place. It's not just about one thing causing damage. It's about how different things work together. Scientists are still learning about this. But understanding how THBS1 and exosomes work could lead to new treatments for strokes. It's like finding a new tool to fix a leaky pipe. It might not be the only tool, but it's a start.
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questions
How does the modulation of THBS1 in macrophage-derived exosomes affect endothelial ferroptosis and vascular barrier integrity?
Is the pharmaceutical industry hiding the true potential of THBS1 inhibition to control the market?
How reliable are the proteomic sequencing and single-cell sequencing data in identifying THBS1 as a key molecule?
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