Somatic
cell reprogramming takes differentiated cells and returns them to a pluripotent state.
Not exact matches
The new research
took adult
cells (skin
cells), exposed them to four genes, and the genes appear to have
reprogrammed the
cells to a pluripotent state.
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.
«Resistance to
reprogramming also helps to explain why
reprogramming takes place only in a very small proportion of the starting
cells.»
Ding's team
took cells called fibroblasts from the connective tissues of mouse fetuses and bathed them in a cocktail of the four polyarginine - tagged proteins for 12 hours, then they removed the
reprogramming proteins for 36 hours, and repeated this cycle four times over.
«The final step was the most unique — and the most difficult — as molecules had not previously been identified that could
take reprogrammed cells the final step to functional pancreatic
cells in a dish.»
This year they succeeded in generating mini-livers, or liver buds, from stem
cells that were
taken from human skin and
reprogrammed to an embryonic state.
In a process called cellular
reprogramming, researchers at Icahn School of Medicine at Mount Sinai have
taken mature blood
cells from patients with myelodysplastic syndrome (MDS) and
reprogrammed them back into iPSCs to study the genetic origins of this rare blood cancer.
The research team
took skin fibroblast tissue from adult mole - rats and
reprogrammed the
cells to revert to pluripotent stem
cells.
These are
cells taken from adult non-muscle tissues, such as skin or blood, and
reprogrammed to revert to a primordial state.
«The discovery of the «brite» fat
cell mechanisms and the specific regulatory areas brings us closer to understanding how
reprogramming of white fat
cells takes place.
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.
«By identifying the areas of the genome that are directly involved in the
reprogramming, we have also identified an important factor in the process — the gene regulatory protein KLF11 (Kruppel Like Factor - 11), which is found in all fat
cells, and we have shown that it is required for the
reprogramming to
take place.»
«To put this into perspective,
reprogramming to induced pluripotency in
cell culture
takes several days to weeks whereas
reprogramming to totipotency in zygotes occurs in less than 24 h,» says Kikuë Tachibana - Konwalski, who devotes her laboratory's research to understanding the molecular secrets of egg
cells and zygotes.
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.
Researchers at the Center for iPS
Cell Research and Application (CiRA), Kyoto University,
took advantage of this strategy by
reprogramming FOP patient
cells and then seeking candidate molecules that could explain how the disease initiates.
To conduct the study, scientists
took dental pulp
cells from donated baby teeth of three children with diagnoses of non-syndromic autism (part of the on - going «Tooth Fairy Project») and
reprogrammed the
cells to become either neurons or astrocytes, a type of glia or support
cell abundantly found in the brain.
«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.
Seeking to
take advantage of these traits, scientists can
reprogram viruses to function as vectors, capable of carrying their genetic cargo of choice into the nuclei of
cells in the body.
In one study, geneticist Joseph Ecker at the Salk Institute in California
took various stem
cell lines
reprogrammed from skin, fat, and other tissues and examined each line's genome for dna methylation, chemical marks that alter how genes are expressed.
This is all it
takes for a so - called precursor fat
cell to have its «epigenetic recipe» on how to correctly develop into a mature fat
cell,
reprogrammed.
Pluripotent stem
cells include embryonic stem
cells, which are derived from early embryos, and induced pluripotent stem
cells, which are made by
reprogramming cells taken from adult tissues such as skin.
Under the direction of Senior Lecturer Yoshinori Yoshida, Funakoshi
took induced pluripotent stem (iPS)
cells that were
reprogrammed from skin
cells and made them into heart
cells.
The problem of this discovery is that only a very small percentage of
cells can be
reprogrammed, the
reprogramming process
takes weeks and its success rate is somewhat hit - and - miss.
In 2006, Yamanaka
took Gurdon's work to the next level by
reprogramming adult mouse skin
cells into induced pluripotent stem
cells.
The ultimate plan is to
take liver
cells from people with diabetes,
reprogram the
cells and reinject them.
Using a process called cellular
reprogramming, the researchers
take a patient's skin
cells, convert them into so - called induced pluripotent stem (iPS)
cells, which can differentiate into all the
cells within the human body.
To create the repository, the researchers are
taking blood
cells from Gulf War veterans and «
reprogramming» them into their «pluripotent» state, which can then be transformed into any type of
cell, from a kidney to a neuron.
Using this approach, immune
cells are
taken from a patient's bloodstream,
reprogrammed to recognize and attack a specific protein found in cancer
cells, then reintroduced into the patient's system, where they get to work destroying targeted tumor
cells.
The first international congress of INGESTEM «Pluripotent stem
cells:
reprogramming and tissue engineering» will
take place in Paris at November 19 - 20, 2015.
Adult stem
cell research does take place at Georgetown, in the Department of Biochemistry and Molecular & Cellular Biology, in addition to groundbreaking stem - like cell research in the Center for Cell Reprogramm
cell research does
take place at Georgetown, in the Department of Biochemistry and Molecular & Cellular Biology, in addition to groundbreaking stem - like
cell research in the Center for Cell Reprogramm
cell research in the Center for
Cell Reprogramm
Cell Reprogramming.
Taking this work a step further, in 2008, they were the first to show that skin
cells could be
reprogrammed into stem
cells (becoming induced pluripotent stem
cells, or iPS
cells), then differentiated into specific dopamine neurons.
Pluripotent stem
cells:
reprogramming and tissue engineering, our first international congress, will
take place in Paris at November 19 - 20, 2015.
After some time during which
reprogramming should
take place, you start to evaluate the outcome and conduct functional assays, such as patch clamp recordings in case you try to obtain neurons to prove that
cells really change their identity.
To answer this question, the Srivastava team
took skin
cells from the family and
reprogrammed them using stem
cell technology into beating heart
cells.
Monday, September 26 10:45 - 11:30 am — Sheng Ding
takes an alternative approach to cellular
reprogramming, adding chemicals to
cells instead of genes.
iPSCs are
cells that can be
take from adult tissue and «
reprogrammed» into embryonic stem
cell (ESC)- like
cells.
Is it possible to
take any
cell in the adult body and directly
reprogram it, skipping the iPSC state, into the final desired
cell type?
When the somatic
cells are initially
reprogrammed with the 4 genes and then allowed to divide, do they go to a blastocyst - like stage in which
cells are
taken to generate and perpetuate the iPS, or is it something different from that?
And what we're finding is when we
take these
reprogrammed skin
cells, we need to compare it to a gold standard.
There are studies on embryonic stem
cells, which can make all the tissues of your body, and people over the past couple years have been able to
take a set of genes and put them in and
reprogram the skin
cells to think they're an embryonic
cell and therefore being able to make all the tissues of your body.
They speculate that because the process of
reprogramming increases the number of
cell divisions that
take place (as compared to what happens in adult skin
cells), there are more opportunities for the
cell cycle checkpoints to correct for the chromosomal breakage.
And at Japan's RIKEN Center for Developmental Biology, one pioneering group is
taking induced pluripotent stem
cells (iPS), mature
cells reprogrammed to return to a state of pure potential, and turning them into RPE
cells.
This strategy
takes advantage of the
cells «somatic memory of origin» and novel
reprogramming strategies to make these
cells an effective and safe source of
cells for the treatment of cartilage defects and osteoarthritis.
Salk researchers
reprogrammed skins
cells taken from a sickle
cell disease patient into induced pluripotent stem
cells (iPSCs), immature
cells capable of developing into any type of bodily tissue.
It
takes only three transcription factors — proteins that turn genes on or off in a
cell — to
reprogram connective tissue
cells into heart muscle
cells in a mouse.
The
reprogrammed cells originally
taken from schizophrenia patients showed the same transcriptional signatures (or underlying biology) as
cells taken from postmortem patients, indicating that the stem
cell - derived brain
cells successfully recapitulated the disease and identifying possible biological variants that contribute to its onset.
Other techniques can
reprogram «adult»
cells in the human body
taken from skin, for example — but the
cells still carry baggage from their previous state.