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, August 26, 2013

Hydrogel Matrix to Support Stem Cell Survival After Brain Transplantation in Stroke

I just focused on the brain transplantation in the title, but its about saving injected stem cells into the brain. What does your doctor think of this?
Are they doing any thinking at all?
http://nnr.sagepub.com/content/24/7/636.short
  1. Jin Zhong, PhD
    1. David Geffen School of Medicine at UCLA, Los Angeles, CA, USA
  1. Albert Chan, MD
    1. David Geffen School of Medicine at UCLA, Los Angeles, CA, USA
  1. Leeron Morad
    1. David Geffen School of Medicine at UCLA, Los Angeles, CA, USA
  1. Harley I. Kornblum, MD, PhD
    1. David Geffen School of Medicine at UCLA, Los Angeles, CA, USA
  1. Guoping Fan, PhD
    1. David Geffen School of Medicine at UCLA, Los Angeles, CA, USA
  1. S. Thomas Carmichael, MD, PhD
    1. David Geffen School of Medicine at UCLA, Los Angeles, CA, USA, scarmichael@mednet.ucla.edu

Abstract

Stroke is a leading cause of adult disability. Stem/progenitor cell transplantation improves recovery after stroke in rodent models. These studies have 2 main limitations to clinical translation. First, most of the cells in stem/progenitor transplants die after brain transplantation. Second, intraparenchymal approaches target transplants to normal brain adjacent to the stroke, which is the site of the most extensive natural recovery in humans. Transplantation may damage this tissue. The stroke cavity provides an ideal target for transplantation because it is a compartmentalized region of necrosis, can accept a high volume transplant without tissue damage, and lies directly adjacent to the most plastic brain area in stroke. However, direct transplantation into the stroke cavity has caused massive death in the transplant. To overcome these limitations, the authors tested stem/progenitor transplants within a specific biopolymer hydrogel matrix to create a favorable environment for transplantation into the infarct cavity after stroke, and they tested this in comparison to stem cell injection without hydrogel support. A biopolymer hydrogel composed of cross-linked hyaluronan and heparin sulfate significantly promoted the survival of 2 different neural progenitor cell lines in vitro in conditions of stress and in vivo into the infarct cavity. Quantitative analysis of the transplant and surrounding tissue indicates diminished inflammatory infiltration of the graft with the hydrogel transplant. This result indicates that altering the local environment in stem cell transplantation enhances survival and diminishes cell stress. Stem cell transplantation into the infarct cavity within a pro-survival hydrogel matrix may provide a translational therapy for stroke recovery.

1 comment:

  1. Stem cells injected into the brain cause massive cell death -- Yikes!

    ReplyDelete