Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Monday, October 28, 2024

Mechanisms of neurogenesis after stroke revealed

 If you have any competence at all in your stroke medicals 'professionals' and hospital there will be immediate research initiated to solve the poor neurogenic response by the SVZ post stroke in humans. All they have to do is contact stroke leadership and get the stroke strategy updated to put this first in line. But since there is NO leadership or strategy in stroke, NOTHING WILL GET DONE!

Mechanisms of neurogenesis after stroke revealed

Researchers at the University of Freiburg have studied what happens immediately after a stroke in the stem cell niche known as the subventricular zone, using a mouse model. This revealed a mechanism that results in fewer newborn neurons from the stem cell niche surviving after stroke, thereby significantly limiting the neurogenic reaction of the subventricular zone to repair the brain. This fundamental understanding of the cellular processes in the brain could help in future to boost the body's own repair to replace lost neurons and ameliorate the consequences of stroke.

In healthy rodent brains, newborn neurons are constantly generated in the stem cell niche, known as the subventricular zone (SVZ). These cells might help to repair a brain that has been damaged by disorders of the central nervous system. After brain damage, the SVZ responds by forming newborn neurons that migrate towards the area of the lesion and could provide cell replacement there. However, after a stroke, the functioning of the body's own repair system, the neurogenic response by the SVZ, is very limited. Researchers headed by Prof. Dr. Christian Schachtrup, professor at the Institute of Anatomy and Cell Biology at the University of Freiburg, and his former doctoral student Dr. Suvra Nath, have studied the mechanisms underlying this limited response to repair the brain.

Stroke negatively influences interaction of microglia and neurons

The vasculature, that is, the system of blood vessels of the SVZ, becomes more permeable after a stroke. As a result, the protein fibrinogen and others reach the stem cell niche, and this in turn influences the local microglia cells. These central nervous system immune cells are immediately activated by the changes in the stem cell niche, affecting the cell cycle progression of the neural stem cells leading to cell death of newborn neurons. "The SVZ stem cell niche is a fragile system. Microglia, the defence cells of the brain, are an integral component of the characteristic SVZ microenvironment and govern the behavior of the neural stem cells. These interactions in the stem cell niche are disrupted after a stroke," explains Schachtrup.

A check test also suggests that the interactions between activated microglia and neural stem cells in the SVZ negatively influence the neurogenic repair: restoring the original SVZ microenvironment increases the neurogenic repair - even after stroke. At the same time, more newborn neurons survive in the SVZ if the activated microglia cells are reduced.

Ameliorating the consequences of stroke

The processes described by the researchers begin very shortly after a stroke. In order to understand them, they had to rely on mouse models. Although the human brain also has an SVZ, new neurons are only produced in the first year of life(not true) and this cell production is dormant after that. The researchers believe it is possible that this production could be reforced by medical intervention.

When we understand the mechanisms of how the neural stem cells are differentiating and how extracellular factors influence the development of newborn neurons, this will bring us closer to promote the endogenous repair of the brain in central nervous system disorders."

Dr. Christian Schachtrup, Professor at the Institute of Anatomy and Cell Biology, University of Freiburg

Next, the researchers want to study interactions between microglia cells and neural stem cells in human organoids. This method is bringing them closer to the goal of understanding similar processes in the human brain.

Source:
Journal reference:

Nath, S., et al. (2024) Interaction between subventricular zone microglia and neural stem cells impacts the neurogenic response in a mouse model of cortical ischemic stroke. Nature Communications. doi.org/10.1038/s41467-024-53217-1.

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