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, November 2, 2020

Pericytes as Cell Therapy for Locomotor Recovery

 I happen to think it would be vastly more important to stop pericytes strangling capillaries in the first week during the neuronal cascade of death thus preventing a lot of damage in the first place. But what the hell do I know? I'm just a stroke-addled stroke survivor. And you know stroke survivors know absolutely nothing about stroke.

Pericytes as Cell Therapy for Locomotor Recovery

 
Abstract

Purpose of Review

The purpose of this review is to explore the rationale and evidence for using pericytes in cell therapy applications to improve locomotor recovery post-injury.

Recent Findings

Pericyte adaptability in form and function aids in maintaining central nervous system homeostasis after injury but can also contribute to pathology. Current cell therapy techniques involve manipulation of endogenous pericytes to enhance their pro-recovery activities and manipulation of exogenous pericytes in vitro for injection post-injury. The mechanisms of pericyte-induced recovery of locomotor function are unclear but seem to involve stabilization of vascular functions and regulation of vascular and axonal growth. Injected exogenous pericytes, manipulated in vitro before injection, could provide neurotropic signals that promote recovery and/or differentiate and take the place of missing neuronal components.

Summary

Pericytes have emerged as novel candidates for cell therapy-mediated tissue recovery. Pericytes are harvestable cells that have the potential to be a readily translatable therapy for locomotor recovery. The field is in a state of infancy. Although promising, at this point only pre-clinical evidence exists. Choosing a consistent and reliable source of pericytes, characterizing them extensively, and then applying these principles in a large animal model of central nervous system injury could help to move the field towards clinical trials.

Introduction

Pericytes have emerged as novel tools for cell-mediated recovery of tissue function [1]. How is it that pericytes, ubiquitous throughout the body, embedded in the basement membrane of capillary walls and often encircling a vessel (Fig. 1) [2, 3] have become a source for cell-based therapy applications? What is the evidence that they can be effective in treating clinical concerns, like enhancing locomotor recovery after brain or spinal cord injury? A review of the unique cell biology of pericytes and the evidence available to date will be helpful in answering these questions.

Fig. 1
figure1

Pericytes are perivascular cells that are embedded in the basement membrane of capillaries throughout the body. a Immunohistochemical image of a capillary within the spinal cord of a neonatal rat pup. Capillaries (isolectin labeling) are green, smooth muscle cells (α-smooth muscle actin labeling) are red, pericytes (PDGFR-β labeling) are magenta, and nuclei (Hoechst labeling) are blue. b Transmission electron microscope image of a pericyte encircling a brain capillary

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