Even cooler, scientists are now able to «reprogram» human
skin cells from patients with neurological disorders and grow them into brain cells [source: Kavli Foundation].
NYSCF Research Institute scientists in collaboration with researchers at the Icahn School of Medicine at Mount Sinai refined a technique to turn
skin cells from patients...
They reprogrammed adult
skin cells from patients with NOTCH1 mutations into a kind of stem cell called induced pluripotent stem cells (iPSCs).
Working at the University of California, Davis, the researchers created a new cellular model for studying Down syndrome by taking
skin cells from patients with Down syndrome and inducing them into a pluripotent state.
First, the researchers took
skin cells from patients and introduced genes to correct the defective mutations.
In the future, we would like to study
skin cells from patients with disorders of motor neurons.
To do so, they converted
skin cells from patients into so called induced pluripotent stem cells.
The researchers, led by University of California, San Diego neuroscientist Mark Tuszynski, took
skin cells from the patients, grew them up in a culture dish and genetically engineered them to make human nerve growth factor (NGF).
«Use of induced pluripotent stem cell (iPSC) technology» — which involves taking
skin cells from patients and reprogramming them into embryonic - like stem cells capable of turning into other specific cell types relevant for studying a particular disease — «makes it possible to model dementias that affect people later in life,» says senior study author Catherine Verfaillie of KU Leuven.
In the present study, her team took
skin cells from patients with lissencephaly and turned them into iPS cells, which they then cultivated under special conditions into neuronal stem cells and neurons that are copies of those in the patients» brains.
The disease model, described in a new study by a UC San Francisco - led team, involves taking
skin cells from patients with the bone disease, reprogramming them in a lab dish to their embryonic state, and deriving stem cells from them.
The two groups took
skin cells from patients and transformed them into the type of brain cells that are affected by Alzheimer's.
Zheng, together with Leah Boyer, then a researcher in Gage's lab and now director of Salk's Stem Cell Core, generated diseased neurons by taking
skin cells from patients with Leigh syndrome, reprogramming them into stem cells in culture and then coaxing them to develop into brain cells in a dish.
In new research, scientists reprogrammed
skin cells from patients with rare blood disorders into iPSCs, highlighting the great promise of these cells in advancing understanding of those challenging diseases — and eventually in treating them.
To develop their «disease in a dish» model, the team took
skin cells from patients with Allan - Herndon - Dudley syndrome and reprogrammed them into induced pluripotent stem cells, which then can be developed into any type of tissue in the body.
«In theory, we could model progression of the disease by reprogramming
skin cells from patients at a range of ages, including before symptoms begin.
For instance, researchers at the Salk Institute in California have taken
skin cells from a patient with the genetic disease Fanconi's anemia, often associated with leukemia.
Adding four genes to a specialized adult cell — such as
a skin cell from a patient — can convert it into an iPS cell.
The team, led by Eggan and Christopher Henderson of Columbia University Medical Center, grew iPS cells by introducing the four genes used in the earlier studies into about 30,000
skin cells from the patient.
A group that included researchers at the Wellcome Trust Sanger Institute and the University of Cambridge, both in the United Kingdom, developed a possible treatment for A1ATD by first reprogramming
a skin cell from a patient into iPS cells, which are embryonic - like cells that can develop into many tissue types.
First, they took adult
skin cells from a patient with an HBB mutation that causes sickle cell disease.
It is now almost routine to grow
skin cells from a patient with, say, a neurological disease; turn them into pluripotent cells in a Petri dish; convert the cells into nerve cells to study the disease process; and contemplate using the cells to repair the same patient's damaged brain.
Not exact matches
According to Science Daily, Dr. Nagy, senior investigator at the Samuel Lunenfeld Research Institute of Mount Sinai Hospital, there is a «new method of generating stem
cells that does not require embryos as starting points and could be used to generate
cells from many adult tissues such as a
patient's own
skin cells.»
They are also getting
skin cells from glioblastoma
patients to make sure the new method works for the people they hope to help, he says.
Skin cells are easy to collect
from patients and share the same genetic blueprint — and disease - causing mutations — as brain
cells.
And other researchers question the need to use
cells from the
patient's own
skin.
The study, published Feb. 5 in Nature Neuroscience, showed that the
patients» nerve
cells — converted directly
from patients»
skin cells — exhibited «symptoms» of the disorder, including DNA damage, dysfunctional mitochondria and
cell death.
Beginning in the 1970s, physicians learned how to harvest
skin stem
cells from a
patient with extensive burn wounds, grow them in the laboratory, then apply the lab - grown tissue to close and protect a
patient's wounds.
Scientists
from the University of Cambridge's Institute for Medical Research obtained
skin cells from 10
patients — seven who had various forms of inherited liver disease, and three healthy controls.
Finally, he would suck out stem -
cell - rich fat
from the
patient's belly and inject it into a layer under the dermis to replenish the fat that keeps
skin elastic and soft.
To test the platform, they obtained
skin cells from consenting
patients at the Center for Duchenne Muscular Dystrophy, all of whom had mutations that fell within the dystrophin gene hot spot.
The investigators obtained further evidence of the critical role of astroglial
cells in Down syndrome by implanting the
skin -
cell derived astroglial
cells from Down syndrome
patients into mice.
In addition to helping understand disease by providing more powerful study models, «what this technology would allow you to do is reprogram a
skin cell, for example,
from a Parkinson's
patient... into a pluripotent
cell and then in a petri dish redirect that
cell into... a neuron» to treat that
patient.
Because neural crest
cells can also be isolated
from skin and hair follicles, OECs could potentially be grown
from a
patient's own
cells.
Researchers can create iPSCs
from a
patient's blood or
skin cells, and use these
patient - specific
cells to study diseases or even create new tissues that could be transplanted back into the
patient as therapy.
The study team removed fibroblasts (
skin cells)
from DBA
patients, and in
cell cultures, using proteins called transcription factors, reprogrammed the
cells into iPSCs.
Unlike the
skin cells from which they originated, the human iPS
cells created
from FOP
patients show increased cartilage formation and increased bone mineralization, two critical steps that are necessary to form mature bone.
Researchers might generate personalized brain organoids
from the reprogrammed
skin cells of individuals with, say, schizophrenia and test which medications work best for
patients with particular genetic profiles of the illness.
Stem
cell source: Obtained
from skin or blood
cells of
patients.
Fragile
skin that blisters easily: 90 percent of the
patients that suffer
from the
skin condition recessive dystrophic epidermolysis bullosa (RDEB) develop rapidly progressing cutaneous squamous
cell carcinomas, a type of
skin cancer, by the age of 55.
This time, instead of using
skin cells, the team reprogrammed lymphocytes (immune
cells)
from six entirely new bipolar
patients, some of whom are known lithium responders.
The technique allows scientists to make stem
cells from, for instance, a
patient's
skin cells.
Since the 1970s tissue engineers have been figuring out how to grow
skin, bone, cartilage, and even parts of vital organs using
cells harvested directly
from patients.
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.
The bacterial peptide found to activate MS
patients» T
cells came
from Pseudomonas aeruginosa, a common inhabitant of human
skin which can infect wounds.
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.
By analyzing
skin cells from achromatopsia
patients and their unaffected family members, the researchers confirmed that the ATF6 mutations were interfering with the signaling pathway that regulates the unfolded protein response.
To determine whether L1CAM has a role in cancer, the researchers looked for its protein in normal
skin cells, cultured noncancerous
cells, and aggressive melanomas
from 11
patients.
Alternative
cell lines, such as induced pluripotent stem
cells generated
from patient skin cells, offer a more accurate window on human biology, he says.
For the first time, scientists can use
skin samples
from older
patients to create brain
cells without rolling back the youthfulness clock in the
cells first.