Human Embryonic Stem Cell - Derived Oligodendrocyte
Progenitor Cell Transplants Improve Recovery After Cervical Spinal Cord Injury.
Not exact matches
The enhanced mice masterfully memorized new objects, swiftly learned to link certain sounds or situations to an unpleasant foot shock, and displayed un-usually savvy maze navigation — signs of mental acuity that surpassed skills exhibited by either typical mice or mice
transplanted with glial
progenitor cells from their own species.
They then
transplanted progenitors of the inner ear
cells into the inner ear of embryonic normal and Connexin 30 knockout mice using glass tubes with optimized tip sizes.
For the other adult patients that might still benefit from a cord blood donor, either two cord blood units are combined for a single
transplant, or more recently, there are some exciting new graft engineering technologies that are emerging to expand stem or
progenitor cells in the laboratory before infusion or modify the
cells in some way to make them more potent at the time of
transplant.
Dr. Viczian has demonstrated that a single extrinsic factor can transform frog skin
cells into retinal stem /
progenitor cells and, further, that the newly made
cells could generate an entire functional eye once they were
transplanted to host embryos.
In addition, when these inhibitory
progenitor cells were
transplanted into apoE4 mice with an accumulation of amyloid beta, prior deficits were alleviated.
In the study, which was conducted in collaboration with researchers at UC San Francisco and published today in the Journal of Neuroscience, scientists
transplanted inhibitory neuron
progenitors — early - stage brain
cells that have the capacity to develop into mature inhibitory neurons — into two mouse models of Alzheimer's disease, apoE4 or apoE4 with accumulation of amyloid beta, another major contributor to Alzheimer's.
Starting with
transplants of human oligodendrocytes in the late 1980s [40], and more recently with populations of human oligodendrocyte
progenitor cells isolated from the developing or adult CNS, or from human embryonic stem
cells, it has been possible to generate extensive myelination upon transplantation into spinal cord injury or into congenital mouse models of hypomyelination [41]--[48].
In this work, we
transplanted hematopoietic stem and
progenitor cells into the substantia nigra of brains of two different mouse models of Parkinson's disease.
In the CNS,
transplanted human neural
progenitor cells derived from prenatal cortex (hNPCctx) display characteristics important for
cell - based rescue of degenerating neurons.
(C) Confocal image of P150 dystrophic inner retina
transplanted with hNPCctx — GDNF and double stained with antibodies against nestin, a neural stem and
progenitor cell marker (green) and human nuclear antigen (red).
Further challenges include the identification of signaling molecules that promote the generation of beneficial populations of astrocytes, identification of appropriate stem and / or
progenitor cell populations that can be the source of such
cells, and determination of whether there are situations in which it is more useful to
transplant astrocytes themselves rather than to
transplant stem or
progenitor cells that might generate astrocytes in vivo in response to signals present in the host environment.
By
transplanting Wnt - activated hematopoietic stem and
progenitor cells (HSPCs) we demonstrated that Muller
cells can be reprogrammed in vivo after fusion with HSPCs.
Writing in Journal of Immunology, lead author and BSI member, Professor Graham Anderson explains, «Post-transplantation, T -
cell progenitors derived from the bone marrow
transplant can struggle to enter the thymus, as if the doorway to the thymus is closed.
The authors
transplanted human cortical ‐ derived neural
progenitor cells engineered to secrete glial
cell line ‐ derived neurotrophic factor (GDNF) into the cortex of a rat model of ALS, where the
cells migrated, matured into astrocytes, and released GDNF.
The researchers then
transplant these
progenitor cells into the hippocampi of mice that carry the apoE4 gene and model aspects of Alzheimer's disease.
These
cells return to a precursor stage following their spontaneous fusion with
transplanted haematopoietic stem and
progenitor cells in damaged retinas.
In preliminary studies, they found that the
transplanted progenitor cells replenish the pool of inhibitory neurons and even improve learning and memory in the mice.