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.

Tuesday, August 29, 2017

How New Blood Vessels Sprout

How will your doctor use this to supply new blood vessels for neurogenesis and stem cells?
http://www.alphagalileo.org/ViewItem.aspx?ItemId=178427&CultureCode=en
IBS biologists discovered a key regulator of normal as well as pathological formation of new blood vessels
New blood vessels branch out of preexisting ones is via a process called angiogenesis. Although this is essential for survival, development and wound healing, on the flip side, it also feeds and progresses malignant tumors, as well as other diseases. IBS scientists at the Center for Vascular Research, within the Institute for Basic Science (IBS), in collaboration with LIM Dae-Sik at KAIST, discovered a key regulator of this process, which could become a potential therapeutic target for treating diseases associated with the formation of new blood vessels.
Cells forming the wall of blood vessels, endothelial cells (ECs), are the main actors of angiogenesis. The formation of a new vascular wall is a multistep process that requires coordinated cell migration, proliferation, and junction formation. ECs need to stretch and move and to do that, they use their own "skeleton", the cytoskeleton. The ECs at the front of the migration route are called tip cells and the ones at the base the stalk cells. Tip cells form extensions that help them to creep into the connective tissue. Then, as the new vessel grows out of the existing one, cells also need to create strong bonds to assure a robust wall. Each step is controlled by several proteins whose behavior is only beginning to be understood.
The research team found out that in the presence of growth stimuli, the proteins YAP and TAZ are critical for sprouting angiogenesis, vascular barrier formation, and maturation. YAP and TAZ work together and they have been re-dubbed YAP/TAZ. YAP/TAZ is negatively controlled by the Hippo signaling pathway, a "molecular conversation" whose role is to adjust the organ size to a normal volume. Curiously, mutations in the proteins of this pathway cause oversized organs, from that the name "hippo".
Scientists found that if they overexpress YAP/TAZ, ECs form an excessive number of extensions and boost an abnormal growth of blood vessels, similarly to a tumor. On the other hand, removing YAP/TAZ from 2 day old mice leads to poorly vascularized retina, vision impairment, and internal bleeding in several areas of the brain. In the latter, the ECs' tips are blunt.
YAP/TAZ promotes cytoskeleton remodeling, as well as distribution and abundance of proteins that cement the junction between ECs. For this reason, YAP/TAZ is essential for the formation of the blood retinal barrier and the blood brain barrier. The former protects the eye from potentially toxic substances present in the blood, and the latter does a similar function to defend the brain.
Since angiogenesis is also the root of several diseases, the team tested adult mice that model a common cause of vision loss in the human elderly population, known as age-related macular degeneration. This disease is characterized by a leaky blood retinal barrier and growth of blood vessels under the retina. In this way, they confirmed that YAP/TAZ is also involved in pathological angiogenesis in adulthood. "Understanding angiogenesis at the molecular level can help us to address pathological angiogenesis in age-related macular degeneration and cancer," said KOH Gou Young, corresponding author of the study.
https://www.ibs.re.kr/cop/bbs/BBSMSTR_000000000738/selectBoardArticle.do?nttId=14843

Attached files

  • New blood vessel sprouting from existing one. Cells at the wall of the blood vessels, called endothelial cells (vanilla color) move and invade new tissue through projections led by the stalk and tip cells. The image also shows pericytes in green and vascular endothelial growth factor (blue circle) and its receptor (Y-shape, blue)

  • YAP/TAZ regulates vascular sprouting and growth. New blood vessels branch out of the main one like thin extensions (right). The process is controlled by YAP/TAZ which regulate the production of other proteins used for the growth and integrity of the new vessels. Normal tissue (right) is compared with tissue lacking YAP/TAZ (left), where the pruned-looking branching are not able to develop.

  • Vasculature in the retina with (right) and without (left) YAP/TAZ. YAP/TAZ is essential for the formation of the blood retinal barrier and mice lacking it suffer from poor vision.

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