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.

Friday, February 14, 2025

Study reveals how glial cells respond to damage in neuron dendrites

 Ask your competent? doctor EXACTLY HOW THIS WILL GET YOU RECOVERED!  If it requires further research, is your doctor capable of getting it initiated? 

Study reveals how glial cells respond to damage in neuron dendrites

Neurons may get all the glory, but they would be nothing without glial cells. While brain cells do the heavy lifting in the nervous system, it's the glia that provide nutrients, clean up waste, and protect neurons from harm.

Now, scientists have discovered a new mechanism by which these crucial supporting players detect and respond to neuron damage. Published in Nature Communications, the study describes how two key proteins allow glial cells to actively monitor the hair-like cilia that extend out of nematode dendrites, so that the glial cells can respond to injuries and prevent damage. The findings may have implications for treating diseases caused by defective cilia, such as polycystic kidney disease.

Fleshing out the pathway by which glia interact with dendrites was our major goal. An important next question is whether one could manipulate these cells to address diseases related to cilia."

Shai Shaham, head of the Laboratory of Developmental Genetics, Rockefeller University

Uncharted territory

Neurons rely on axons and dendrites for communication; axons send messages out, while dendrites receive those incoming, some with the help of cilia extending from their tips. Cilia detect odors, light, and other stimuli.

Scientists have studied how glial cells keep axons in shape. But comparatively few studies have investigated how glia protect and maintain dendrites and their delicate cilia. Knowing that dendrite structure changes correlate with learning and memory, and that dysfunctional cilia are at the heart of a family of disorders known as ciliopathies, Shaham and colleagues set out to fill that crucial knowledge gap .

"We knew essentially nothing about the interactions between glial cells and dendrites, but they matter just as much as axons," Shaham says. "You need something to receive signals, too."

The team chose to study glia, dendrites, and cilia in the nematode C. elegans, a model organism cherished by basic researchers for its straightforward genetics and well-studied biology. An additional advantage here was that nematodes have cilia only on the ends of their dendrites, simplifying the work of homing in on what happens to dendritic cilia when glia clock out. "C. elegans is a powerful model, because we can use it to explore everything from molecules to behavior," says Katherine Varandas, a postdoctoral fellow in Shaham's lab and lead author of the study. "Through studying nematodes we can decipher very specific dendrite and glia interactions."

Moving up the tree of life

For the study, the team used CRISPR to engineer nematodes with disrupted cilia or altered glial responses, and then tracked glia in-action using fluorescence microscopy. Then, to figure out how glia respond to normal and cilia-stunted nematodes, they employed RNA sequencing to monitor gene expression changes and electron microscopy to observe structural changes.

They found that glial cells respond to damaged cilia by accumulating excess extracellular matrix proteins and altering gene expression. Specifically, they discovered a new signaling pathway involving DGS-1, a neuronal protein, and FIG-1, a glial protein. These two proteins appear crucial to monitoring cilia integrity-mutations in either trigger glial responses even without cilia damage.

The findings broaden our understanding of glial functions, with potential implications extending far beyond nematodes. Indeed, the structural and functional similarities of sensory organs across species suggest that similar mechanisms for keeping cilia safe may exist in mammals, where glial cells have been shown to interact with similar dendritic structures. The present study could therefore lay the groundwork for exploring glia-dendrite interactions across species, with potential implications for humans suffering from ciliopathies.

"We hope to move these studies into mammals next," Varandas says. "Sensory organs, which include cilia-decorated dendrites surrounded by glia, are highly conserved across evolution and share striking similarities to one another, providing a fascinating direction for future research."

Source:
Journal reference:

Varandas, K. C., et al. (2025). Glia detect and transiently protect against dendrite substructure disruption in C. elegans. Nature Communications. doi.org/10.1038/s41467-024-55674-0.

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