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.»
As I stated in my original article, prior to conducting experiments with human
cells, ANT - OAR techniques would need to be rigorously tested in animal models to establish a procedure that guarantees with reasonable certainty that an
embryo is not
generated.
No
embryo has been
generated, no organism «cloned» if ANT - OAR succeeds in its goal of producing nothing other than pluripotent stem
cells.
Embryonic stem
cells are scientifically and medically interesting because they are «pluripotent» (capable of
generating many
cell types), but they are not the same as totipotent single -
cell embryos.
Should the ANT - OAR proposal work, the alterations made to the adult nucleus will ensure that the
cell produced by ANT - OAR enters immediately into a restricted, pluripotent state, without ever
generating a totipotent
embryo.
Human cloning has been proposed as a means of
generating human
embryos that can be destroyed to obtain embryonic stem
cells.
We can compare the diverse tasks performed by a colony to the many proteins
generated by gene transcription, to various
cell types of a developing
embryo, or to the firing patterns of neurons in the brain.
Despite the time it took to develop a successful hESC -
generating technique — and the interest in iPS
cells as an egg and
embryo - free alternative — Mitalipov's work is important.
The fused
cell behaves like an
embryo and
generates hESCs.
In the paper, published in the now - defunct online journal e-biomed, West, Lanza and their colleagues showed that they could pull a nucleus from a human egg
cell, replace it with a whole adult ovarian
cell and
generate an
embryo that divided into six
cells.
Goats as Drug Factories Initially, GTC
generated transgenic goats by microinjecting into the developing nucleus of a one -
cell embryo a gene encoding the desired human protein (along with DNA that promotes activation of that gene in milk).
Indeed, the in vitro -
generated PGCs offer millions of
cells for scientists to study, instead of the 40 or so that can be obtained by dissecting early
embryos, says Hanna.
In a paper published online yesterday in Stem
Cells, the researchers report that they succeeded in generating pluripotent human ES cell lines — i.e., cells that can develop into many different kinds of cells — from one of the 13 late - arrested emb
Cells, the researchers report that they succeeded in
generating pluripotent human ES
cell lines — i.e.,
cells that can develop into many different kinds of cells — from one of the 13 late - arrested emb
cells that can develop into many different kinds of
cells — from one of the 13 late - arrested emb
cells — from one of the 13 late - arrested
embryos.
Organlike tissue bits can be
generated from pluripotent stem
cells that are either plucked from
embryos or created by taking a person's adult skin or blood
cells and chemically inducing them to revert to an embryonic - like state.
Single -
cell mouse
embryos were infected in vitro with recombinant lentiviral vectors to
generate transgenic mice carrying the green fluorescent protein (GFP) gene driven by a ubiquitously expressing promoter.
The finding potentially paves the way for scores of labs to
generate new stem
cell lines without cloned
embryos, which had long been considered the only realistic way of making human stem
cells in the short run.
Then somatic
cell nuclear transfer
generated pig
embryos carrying this genetic alteration.
In addition, they also found that a factor called SHORT SUSPENSOR (SSP),
generated in the sperm
cell, is important for
cell division of the zygote and development of the
embryo.
Opponents have argued that the law should be rescinded since embryonic stem
cells can now be
generated from induced pluripotent stem
cells, a technique that does not involve human
embryos.
Australian researchers have so far
generated over 50 embryonic stem
cell lines from surplus
embryos, and three research groups have been licensed to attempt somatic
cell nuclear transfer.
At some point in their development, all
embryos — whether human, chimp, rat, frog, or slug — must have a single first
cell committed toward
generating neurons.
«We are now in a position to be able to
generate patient - and disease - specific stem
cells without using human eggs or
embryos,» Shinya Yamanaka, leader of one of the research teams at Kyoto University in Japan, said in an e-mail interview.
They have
generated excitement over the past few decades because scientists can study them in the laboratory to discover the genetic switches that control the development of specialized tissues in the
embryo and fetus, and also because of their potential to replace body tissues that have broken down, such as pancreatic
cells in those with diabetes or heart muscle
cells in those with congestive heart failure.
Stem
cells obtained in mice also show totipotent characteristics never
generated in a laboratory, equivalent to those present in human
embryos at the 72 - hour stage of development, when they are composed of just 16
cells.
These «totipotent - like» stem
cells are able to
generate not only all
cell types within a developing
embryo, but also
cell types that facilitate nutrient exchange between the
embryo and the mother.
«This data tell us that our stem
cells are much more versatile than Yamanaka's in vitro iPSCs, whose potency
generates the different layers of the
embryo but never tissues that sustain the development of a new
embryo, like the placenta,» said the CNIO researcher.
With a tweak to the technique that cloned a sheep in 1996, scientists have
generated stem
cells in the lab that genetically match those found in human
embryos.
«We are now in a position to be able to
generate patient - and disease - specific stem
cells, without using human eggs or
embryos,» says Shinya Yamanaka of the University of Kyoto, who led the Japanese team.
Crucially, the tissues can be
generated without having to extract
cells from human
embryos, a major ethical objection that has obstructed stem
cell research until now.
Scientists in Canada and Scotland have developed a virus - free method for
generating embryonic - like stem
cells that does not involve destroying
embryos.
To ensure that donor and host tissues could be easily distinguished, we
generated EFTF - expressing
cells from transgenic
embryos constitutively expressing a variant of yellow fluorescent protein (Venus YFP)[10].
The most radical news at the conference was the first reported use of CRISPR / Cas9 to
generate precise genome edits (changing only a single base pair) in two genes, not only in
cell lines in vitro, but also in specific tissues of
embryos in ovo.
Researchers have discovered a gene in zebrafish so powerful it can be used to redirect the fate of
cells in the developing
embryo to become beating heart
cells, suggesting that a similar gene in humans could be used to
generate heart
cells in culture for transplant in ailing people.
Each of these germ layers is responsible for
generating certain
cell types as the
embryo develops.
Canada's central repository for cryopreserved ES
cells, spermatozoa, ova,
embryos, and tissue DNA
generated by Canada's mouse genome effort.
All organisms develop from
embryos: a
cell divides
generating many
cells.
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.
Cardiovascular progenitor
cells (CPCs) are
generated naturally as the heart forms in an
embryo and give rise to a selection of different kinds of heart
cells.
The team that
generated the insulin - producing embryonic stem
cell line, e.g., had a success rate of under six percent, using 71 eggs to produce four stem
cell lines from the
embryos they created and destroyed.
This must be accomplished by using a process known as germ - line transmission, where the primordial germ
cells (PGCs) of an early
embryo are edited, grown in cultures, and then reproductively transmitted through surrogate host parents to
generate live, engineered birds.
The researchers show that if the number of
cells aggregated initially is similar to that of a mouse
embryo, the
cells generate a single axis and this serves as a template for a sequence of events that mimics those of the early
embryo.
One of those teams created a cloned
embryo from the somatic
cells of a diabetic patient; this
embryo was then destroyed in order to
generate an insulin - producing embryonic stem
cell line.
He was also a Fulbright Scholar, and was part of the team that cloned the world's first human
embryo, as well as the first to successfully
generate stem
cells from adults using somatic -
cell nuclear transfer (therapeutic cloning).
Izpisua Belmonte and colleagues published work in the journal Nature last year reporting that they had been able to integrate human stem
cells into early - stage mouse
embryos so that the human stem
cells began the first stages of differentiation — they appeared to begin the process of
generating precursors of the body's various tissues and organs.
Embryonic stem (ES)
cells are karyotypically normal,
embryo - derived
cell lines that are pluripotent, i.e. capable of
generating all the
cell types of the future organism, but not the extra-embryonic lineages.
Stem
cells can be derived either from human
embryos or, in a really wonderful new discovery, they can be
generated from a patient's own skin
cells.
Human pluripotent stem
cells derived from embryos (human Embryonic Stem Cells or hESCs) or generated by direct reprogramming of somatic cells (human Induced Pluripotent Stem Cells or hiPSCs) can proliferate almost indefinitely in vitro while maintaining the capacity to differentiate into a broad diversity of cell t
cells derived from
embryos (human Embryonic Stem
Cells or hESCs) or generated by direct reprogramming of somatic cells (human Induced Pluripotent Stem Cells or hiPSCs) can proliferate almost indefinitely in vitro while maintaining the capacity to differentiate into a broad diversity of cell t
Cells or hESCs) or
generated by direct reprogramming of somatic
cells (human Induced Pluripotent Stem Cells or hiPSCs) can proliferate almost indefinitely in vitro while maintaining the capacity to differentiate into a broad diversity of cell t
cells (human Induced Pluripotent Stem
Cells or hiPSCs) can proliferate almost indefinitely in vitro while maintaining the capacity to differentiate into a broad diversity of cell t
Cells or hiPSCs) can proliferate almost indefinitely in vitro while maintaining the capacity to differentiate into a broad diversity of
cell types.
Once Woolly Mammoth - like traits appear sufficiently in stem
cell derived tissues, the Church Lab can begin experiments to
generate embryos, possibly through stem
cell embryogenesis.
Both approaches have weaknesses — one requires
embryos and the other requires tedious genetic manipulations that might compromise the quality of the
generated cells and therefore, rapid clinical application.