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.

Thursday, May 28, 2020

Brain transforms natural killer cells that exacerbate brain edema after intracerebral hemorrhage

Sounds like a great idea to do some followup research on humans. But with NO LEADERSHIP ANYWHERE IN STROKE, nothing will occur. 

Brain transforms natural killer cells that exacerbate brain edema after intracerebral hemorrhage

Qiang Liu, Zhiguo Li, Minshu Li, Samuel Shi, Zilong Zhu and Xiaoan Zhang

Abstract

Perihematomal edema (PHE) occurs within hours after intracerebral hemorrhage (ICH), leading to secondary injury manifested by impaired blood-brain-barrier (BBB) integrity and adjacent tissue destruction. To dissect mechanisms underlying PHE formation, we profiled human and mouse perihematomal tissues and identified natural killer (NK) cells as a predominant immune cell subset that outnumbers other infiltrating immune cell types during early stage of ICH. Unbiased clustering of single cell transcriptional profiles revealed two major NK cell subsets in the brain following ICH that possess either high cytotoxicity or robust chemokine production features, which distinguish them from NK cells in the periphery. NK cells exacerbate BBB disruption and brain edema after ICH via cytotoxicity toward cerebral endothelial cells and recruitment of neutrophils that augment focal inflammation. Thus, brain-bounding NK cells acquire specific features that contribute to PHE formation and neurological deterioration following ICH.(How do we stop this?)

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