Although the success
of the grafted cells is exciting, there's still a lot of work to be done to conclude whether the extra grey matter actually improves cognition.
«What was really exciting is that in both old and young brains, a small percentage
of the grafted cells retained their «stemness» feature and continuously produced new neurons,» said Bharathi Hattiangady, assistant professor at the Texas A&M College of Medicine and co-first author of the study.
To apply in vivo imaging tools for non-invasive monitoring of the survival and growth
of the grafted cells, as well as tools to reveal adverse immune / inflammatory reactions to the graft;
However, the Connexin 30 knockout mice had more grafted cells than the normal mice, and
some of the grafted cells were found to express CONNEXIN 30.
Future work will attempt to increase the number
of grafted cells and improve hearing ability.
The fact that Connexin 30 knockout mice had a higher number
of grafted cells than normal mice, and that some of the grafted cells expressed CONNEXIN 30 is a very important finding when considering cell transplantation as a treatment for hereditary hearing loss caused by CONNEXIN deficiency.
Not exact matches
«It's important that it all be viable — if not, not only might
cells die in the center
of the
graft, but they can release bad signals to remaining healthy
cells in an «apoptotic cascade,» essentially saying, «Conditions are horrible, let's commit suicide.»»
«Finding the optimal conditions to avoid interfering with immune
cells working to eradicate cancer while preventing
graft rejection and GVHD is the holy grail
of bone marrow transplant,» says Leo Luznik, M.D., associate professor
of oncology at the Johns Hopkins Kimmel Cancer Center.
The researchers also found that arteries and veins from the macaques» hearts grew into the new heart tissue, the first time it has been shown that blood vessels from a host animal will grow into and nurture a large stem -
cell derived
graft of this type.
This image shows an implanted
graft of cardiac
cells derived from human stem
cells (green) meshed and beat with primates» heart
cells (red).
Last week, the woman, who is in her 70s, had a patch
of the
cells measuring 1.3 × 3 millimetres
grafted into her eye in a 2 - hour operation.
In this pilot study to test the safety
of putting iPS - derived
cells into humans, the six are all receiving a
graft of new retinal pigment epithelial
cells, which serve to maintain the eye's light - sensing
cells.
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.
Lymphocytes in the
grafts of undifferentiated iPS
cells were also expressing relatively high levels
of genes known to be involved in hostile immune responses.
In contrast, lymphocytes in both types
of endothelial
cell grafts expressed higher levels
of genes known to be involved in dampening the immune response and inducing self - tolerance.
Historically, clinicians evaluating a patient for transplant have sought to identify donor
cells that are perfectly matched to the patient's
cell type, which is considered to be the optimal approach to help ensure successful outcomes and to minimize risk
of graft - versus - host disease (GVHD), a serious and potentially life - threatening complication that occurs when the donated immune
cells attack the patient's
cells as foreign tissue.
On the flipside, targeting this growth factor or BCL - 2 could reduce NK
cell numbers and offer potential therapies for immune disorders such as some types
of autoimmune diseases, sepsis or
graft versus host disease, a side effect
of bone marrow transplants.
When
grafted onto bald mice, the
cells produced not only furry tufts but stretches
of skin complete with the oil - producing glands that help keep it supple as well.
Currently,
grafts are either sheets
of skin taken from a donor site on the body, or layers
of cells cultured in vitro from the patient.
Hina had developed the devastating immune reaction known as
graft - versus - host disease, in which donor
cells attack the walls
of the gut, skin, lungs, liver, and sometimes — though rarely — even the patient's brain.
«The immune response to the iPS - derived endothelial
cells and the aortic endothelial
cells, and the longevity
of the
grafts, was very similar,» said Kooreman.
They found that, while the
grafts of undifferentiated iPS
cells harbored large numbers
of T
cells of only a few specificities — indicating a robust immune response — those found in
grafts of the two types
of endothelial
cells were more diverse, suggesting a more limited response associated with a phenomenon known as self - tolerance.
«Preventing
graft - versus - host disease and relapse after transplant requires a difficult balance
of eliminating the bad, overactive effector T
cells, without suppressing the good, regulatory T
cells,» said Kean, who is also an associate professor
of pediatrics at the University
of Washington School
of Medicine and a member
of the Fred Hutchinson Cancer Research Center.
The treatment — a whole - body
graft of genetically modified stem
cells — is the most ambitious attempt yet to treat a severe form
of epidermolysis bullosa (EB), an often - fatal group
of conditions that cause skin to blister and tear off at the slightest touch.
Two approaches to fat
grafting — injection
of fat
cells versus fat - derived stem
cells — have similar effects in reversing the cellular - level signs
of aging skin, reports a study in the April issue
of Plastic and Reconstructive Surgery ®, the official medical journal
of the American Society
of Plastic Surgeons (ASPS).
But stem
cell biologist and physician Michele De Luca
of the University
of Modena and Reggio Emilia in Italy and his colleagues have been developing a way to counteract an EB - causing mutation by inserting a new gene into the
cells used for
grafts.
«Given the serious threat
of graft - versus - host disease, new approaches to make stem
cell transplants safer for patients remain a critical unmet need,» said Dr. Leslie Kean, the trial's principal investigator and associate director
of the Ben Towne Center for Childhood Cancer Research at Seattle Children's.
The researchers found that PAI - 039 inhibited the migration
of cultured human coronary artery smooth muscle
cells, and prevented the development
of blockages in arteries and bypass
grafts in mice.
In fact, the new approach is similar to an established treatment for severe burns, in which sheets
of healthy skin are grown from a patient's own
cells and
grafted over wounds.
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.
When they
grafted a set
of cells from the region that they called the «organizer» into the side
of another embryo, a second body would form, joined to its host like a Siamese twin.
To do this, they switched from using dead tumour
cell samples to patient - derived tumour
cell lines, in which fresh samples
of a person's tumour are
grafted onto mice and grown to the required volumes.
One
of the biggest challenges for medical researchers studying the effectiveness
of stem
cell therapies is that transplants or
grafts of cells are often rejected by the hosts.
A new test may reveal which patients will respond to treatment for
graft versus host disease (GVHD), an often life - threatening complication
of stem
cell transplants (SCT) used to treat leukemia and other blood disorders, according to a study led by researchers at the Icahn School
of Medicine at Mount Sinai and published online today in the journal Lancet Haematology and in print in the January issue.
Wartman has a chronic form
of graft - versus - host disease (GVHD), a debilitating consequence
of blood stem
cell transplants.
Another approach to taming the donor
graft relies on a mixture
of anti — T
cell anti-bodies called antithymocyte globulin, which is produced in horses or rabbits.
Now, in a study recently published in the journal PLOS ONE, a team
of scientists from VCU Massey Cancer Center have shown a genetic relationship between the reactivation
of hCMV and the onset
of graft - versus - host disease (GVHD), a potentially deadly condition in which the immune system attacks healthy tissue following a bone marrow or stem
cell transplant.
Given to the patient shortly before the transplant, the infusion
of antibodies theoretically reduces the host's residual T
cells, minimizing the risk
of graft rejection while eliminating T
cells from the donor to thwart GVHD.
Additionally, it is possible to take small pieces
of the patient's skin, expand these in the laboratory and then
graft them back onto the patient as very thin sheets
of cells.
A team led by the Hutch's Marie Bleakley and by Warren Shlomchik
of the University
of Pittsburgh School
of Medicine in Pennsylvania removes naïve T
cells from
grafts with a magnetic system that uses monoclonal antibodies bound to iron beads.
«The unique aspect
of our procedure, which no one else in the world is doing, is the formation
of blisters as the source
of donor
cells combined with laser surgery to prepare the
grafted areas.
The results, published online today in the Proceedings
of the National Academy
of Sciences, suggest that lacing the
grafts with stem
cells enhances blood flow and boosts the production
of molecules that make and maintain erections, all
of which makes for a better penis reconstruction.
That approach, which shuts down the hyperactive donor T
cells when they first arrive, has not only allowed patients to tolerate
grafts from increasingly mismatched hosts but, in several recent studies, has also cut rates
of severe acute and chronic GVHD to less than 15 %.
The research team tested the hypothesis by transplanting
cells onto the surface
of mouse bone
grafts and studying the
cell behavior both in vivo — inside the animal — and in vitro — outside the body.
The current research team, which includes Dr. Minoda and Dr. Hiroki Takeda
of Kumamoto University, and several researchers from Keio University, have successfully
grafted human iPS - derived
cells into the inner ear
of embryonic mice, a feat with a high level
of technical difficulty.
For example, he says, researchers studying infertility have
grafted human testis and ovary
cells under the skin
of animals in an effort to better understand their development.
The team conducted investigations by
grafting low - metastatic (LM) and high - metastatic (HM) melanoma tumour
cells under the skin
of mice.
«We preferentially delete «naive T
cells», since they are the main subset
of white blood
cells that reject
grafts,» Strober says.
Studies have shown that the clinical success
of transplantation depends on the number and percentage
of limbal stem
cells in tissue
grafts.
It has taken more than five years
of graft, but at long last approval has been given for the first clinical trial using human embryonic stem
cells (hESCs).