In the present work, the teams led by Michael Ewers (ISD) and EMBO Member Christian Haass (DZNE) focussed on the TREM2 protein, which functions in specialized brain immune cells called microglia that clear toxic material resulting from
nerve cell injury.
Not exact matches
Serious trauma to the spinal cord can bring on paralysis even though many
nerve cells survive the initial
injury.
In the new study, Zigmond and colleagues found damaged
nerve cells produce a stream of molecular lures that specifically attract neutrophils to
injury sites in mice.
Immune
cells are normally associated with fighting infection but in a new study, scientists have discovered how they also help the nervous system clear debris, clearing the way for
nerve regeneration after
injury.
Results from the new study suggest immunostimulant molecules that target neutrophils at
nerve injury sites might enhance clean - up and promote
nerve cell repair.
«We came up with a list of potential cellular candidates that could be compensating for the loss of these specific macrophages and used several different tests to determine which
cells were clearing away the
nerve debris after
injury,» Lindborg said.
Yonju Ha, a lead author of this article, said that further studies on this receptor and its role in white blood
cell recruitment following tissue
injury may aid in the development of new interventions for diseases associated with
nerve injury, such as TON, stroke, diabetic retinopathy and glaucoma.
When a spinal cord
injury takes place, extensions of
nerve cells from the brainstem — the region of the brain where the command and coordination for urination takes place — become disconnected from
cells in the spinal cord that control the muscles that squeeze or relax the bladder and open and close the urethra.
In the current study, Yu - Shang Lee, PhD, of the Cleveland Clinic, together with Jerry Silver, PhD, of Case Western Reserve Medical School, and others, used a chemical that promotes
cell growth along with a scar - busting enzyme to create a more hospitable environment for the
nerve graft at the
injury site.
Delivering a single injection of a scar - busting gene therapy to the spinal cord of rats following
injury promotes the survival of
nerve cells and improves hind limb function within weeks, according to a study published April 2 in The Journal of Neuroscience.
The many functions of astrocytes include protecting the brain from
injury and harmful agents and providing essential support for
nerve cells.
After other researchers reported that bone marrow stem
cell therapy led to a modest but promising 5 percent improvement in the regeneration of sensory
nerve fibers in rats with spinal cord
injuries, he performed a critical reality check.
The gene in question, apolipoprotein E (apoE), codes for a protein in the brain's astrocyte
cells that seems to help spur
nerve cell growth and clear up debris from neuronal
injuries brought by head trauma, stroke, or cerebral hemorrhage.
The study introduced here focused on a population of support
cells in the spinal cord that helps to protect surviving
nerve cells (neurons) after
injury: oligodendrocytes and their precursor
cells.
Understanding the coordinated development of motor neurons and glia may inform ways to prod stem
cells into generating more glia after someone suffers an
injury with
nerve damage.
During an early clinical trial at the Miami Project last year, researchers took Schwann
cells from an easily accessible sensory
nerve in a patient's leg, grew them in culture and injected them at the point of the spinal cord
injury.
In that work, scientists removed olfactory ensheathing
cells from the noses of dogs with complete spinal cord
injuries, and injected them at the site of the severed
nerves.
When scientists gave mice an oral drug called LM11A - 31 (designed to prevent neural degeneration in Alzheimer's patients) just hours after a complete spinal cord
injury, it limited the death of
cells that protect
nerve fibers, allowing test rodents to retain their ability to walk and swim.
A study published in
Cell last year demonstrated that human and rat stem
cells could be grafted onto the spinal cord of paralyzed rats, forming new
nerves capable of communicating across the
injury site.
Their breakthrough, published today in the scientific journal PLoS Biology, could eventually help develop tools to repair
nerve cells following
injuries to the nervous system (such as the brain and spinal cord).
Previous research has described at least some of the fundamental processes involved in healthy, on - going peripheral
nerve growth regeneration, including the critical role of mitochondria — cellular organelles that produce adenosine triphosphate (ATP), the energy - carrying molecule found in all
cells that is vital to driving
nerve recovery after
injury.
The
injuries crush and sever the long axons of spinal cord
nerve cells, blocking communication between the brain and the body and resulting in paralysis below the
injury.
Neuroscientists have long believed that scar tissue formed by glial
cells — the
cells that surround neurons in the central nervous system — impedes damaged
nerve cells from regrowing after a brain or spinal cord
injury.
Researchers focused on
injury to
cells in the peripheral nervous system (PNS)-- the crucial network of
nerves outside the brain and spinal cord.
Two weeks after the rats sustained their
injuries, Schwartz's group found that the number of surviving
cells in the damaged
nerves of these rats was three times higher on average than in rats with similar damage that received a placebo injection.
Burn victims or those with spinal cord
injuries might be provided with replacement skin or
nerve tissue grown from their own body
cells.
Ten people will receive injections into the
injury site of hESC - derived oligodendrocyte progenitor
cells, which stimulate the growth of new and severed
nerves and recoat damaged
nerves with myelin.
The study showed that a peripheral
nerve injury in rats sends a message from damaged
nerve cells to spinal cord immune
cells known as glial
cells, which normally act as «housekeepers» to clear out unwanted debris and microorganisms.
To regain function, connections from the brain to the spinal cord must regrow, different types of immune
cells have to clear the
injury site, and stem
cells in the spinal cord need to generate new
nerve cells, which then connect to the muscles.
Macrophage depletion alters the blood —
nerve barrier without affecting Schwann
cell function after neural
injury.
These
cells have the ability to cross the blood - brain barrier and travel directly into the nervous system to improve blood flow to the brain and repair some of the
nerve damage which has occurred as a result of your degenerative disease or neurological
injury.
By this, researchers demonstrated that a peripheral
nerve injury in rats would send a message from the damaged
nerve cell to special spinal cord immune
cells called «glial
cells».
There's no retinal ganglion
cell regeneration or replacement after optic
nerve injury.
When an axolotl suffers a spinal cord
injury, nearby
cells called glial
cells kick into high gear, proliferating rapidly and repositioning themselves to rebuild the connections between
nerves and reconnect the injured spinal cord.
In particular, we are asking how molecules that are important in eye development both prevent and protect against damage in disease states such as AMD and encourage regeneration of
cells and their
nerve fibers after
injury.
He also studies how
nerve cells can form new connections to neighboring
nerve cells after
injury.
By contrast, when a human suffers a spinal cord
injury, the glial
cells form scar tissue, which blocks
nerves from ever reconnecting with each other.
Searching the entire genome, a Yale research team has identified a gene that when eliminated can spur regeneration of axons in
nerve cells severed by spinal cord
injury.
He has also made fundamental contributions to understanding the role of apoE in the nervous system, specifically in
nerve injury and regeneration and in the remodeling of neurites on neuronal
cells.
The Yale team found more than 580 different genes that may play a role in regeneration of axons in
nerve cells, something that rarely occurs in adult mammals but is of vital interest to scientists hoping to repair
injuries to the central nervous system.
Prior research had developed a number of new compounds making use of a novel drug discovery paradigm which begins with natural products extracted from plants; it then entails selecting synthetic derivatives which demonstrate efficacy in multiple assays testing protection against different factors of the
nerve cell damage and death which take place in brain
injuries and in age - associated neurodegenerative conditions.
As with stroke, CNB - 001 was again discovered to maintain the critical signalling pathways needed for
nerve cell survival, and also the connections between
nerve cells which are lost with the
injury.
Escalated regeneration in sciatic
nerve crush
injury by the combined therapy of human amniotic fluid mesenchymal stem
cells and fermented soybean extracts, Natto.
Excitotoxicity is a pathological process where glutamic and aspartic acid cause an over-activation of your
nerve cell receptors, which can lead to calcium - induced
nerve and brain
injury.
Ginkgo may directly stimulate
nerve cell activity, protecting
nerve cells from further
injury.
Student, «Characterizing the macrophage response to peripheral
nerve injury» Gat Rauner, Postdoc Assoc., «
Cell Hierarchy, Lineage Commitment and Differentiation in the Bovine Mammary Gland» Lunch provided with sign up - please contact Sue Williams at
[email protected] or 256-5600
Effects on Brain Development from Terbutaline, Pesticides Both chemicals independently caused brain
injuries not seen in the control rats, including the loss of brain
cells and the
nerve cell projections critical to communication among neurons; and the effects persisted into adulthood.
Most spinal cord
injuries are permanent because spinal
nerve cells do not regenerate like other body
cells, so the damage is irreversible.
As scientists continue to explore the
injury and recovery process of spinal cord
injuries, experimental treatments may be available to stop
cell death, control swelling and
nerve regeneration.
Common types of head
injuries include traumatic brain
injuries, tears of the brain, skull fractures, scalp
injuries, concussions,
nerve cell damage and blood swelling between the brain and the skull.