\ n3) There are «pluripotent» stem cells which are created from skin cells and offer the potential for
becoming different cells similar to the hypothetical benefits of embryonic stem cells, but they do NOT involve any moral controversy.
«Growing stem cells on synthetic surfaces with different levels of compliance showed that stem cells would
become a different cell type depending solely on the mechanical environment they perceive.
However, in a few cases it has been shown that a fully differentiated cell can actually
become a different cell type; this process is called transdifferentiation (Graf and Enver, 2009).
Not exact matches
If human brains are like body's
cells, there is a natural point of specialization, in which new systems break away and form similar but slightly
different branches, as
cells in a body
become fingers, feet, hands, etc..
Cells in the body take account of their environment and
become different as a result.
These
cells, which can
become several
different types of blood
cells, are similar to the specialized stem
cells found in bone marrow that can churn out new blood
cells.
Using a mouse model, the team also demonstrated that two processes during neurodevelopment are regulated by the gene: proliferation — the replication of neuronal stem
cells that have the potential to
become multiple
different kinds of
cells, including neurons — and migration — the movement of neurons to specific locations in the brain during development.
The results, which focus on two choices near the start of embryo formation, show that, when
cells are making decisions about what to
become, there is greater variation in the activity of the genes in
different cells — the same genes may be turned on in some
cells and off in others.
This process of making similar
cells become different is called symmetry breaking.
Cells become different as a result of a long sequence of biochemical choices made before we're born.
Stem
cells are capable of
becoming many
different tissue types, including neurons.
If the contact allergen remains a long time — as was the case with the patient's implant —
different inflammatory
cells and molecules
become active at the site of the reaction.
Dolmetsch exposes these stem
cells to a variety of
different growth factors that mimic those that induce stem
cells to
become neurons during normal development.
Adult stem
cells: They have less flexibility and «stemness» to change into
different cell types, but they can still produce new
cells, specialized to
become part of a particular organ or tissue, such as muscle
cells or neural
cells.
To create
different cell types in the lab, stem
cells must be coaxed down the road of determination — the branching paths that fetal
cells normally travel to
become neurons, skin
cells, muscle
cells, or any number of other
cell types.
Depending on the concentration of cannabinoids and the activity of two
different receptors, the islets
became larger or smaller, while the alpha
cells, usually located outside the islets, were able to migrate inside,» explains Dr. Katarzyna Malenczyk fom the Nencki Institute, the first author of the publication.
As the animal moves,
different subpopulations of these
cells become active depending on distance and direction, creating an internal map of its trajectory.
Many
different compartments within the bacterial
cells or between the
cell membrane and the bacteria's
cell wall also
became apparent.
By exposing the
cells to
different chemical cocktails, the team encouraged some of them to
become brain organoids and others to
become blood vessel
cells.
Sheltzer's team proposes that these
cells rapidly evolved to acquire
different mutations that would confer a survival benefit — perhaps enabling them to grow in new environments, just as cancer
cells that
become metastatic evolve so as to be able to detach from their tissue of origin and grow at
different sites in the body.
«The organization of
cell colonies and phenotypic switching between
different types of colonies
becomes a lot more flexible and rapid with reversible aneuploidy than if it depended on random mutations in the genes,» Skupin says.
Some scientists believe the ability to grow
different cell types started animals on the evolutionary road to
becoming humans.
«But then when we do the experiment again and start changing protein levels, the ratio of these
cells becomes very
different.»
These findings will open up new ways to improve the efficiency of
cell reprogramming and to drive stem
cells to
become different types of specialised
cell.
The central question is how, in the human organism for example, 100 000 genes have been orchestrated to yield about 250
different cell types, which then
become assembled as the human body.
For instance, the trials underway in China and Australia use neural progenitor
cells that can grow to
become a variety of
different cell types.
Additionally, ERCs were reported to be able to differentiate into, or
become,
cells from the three
different germ layers (see the previous post on MSCs for more details): mesoderm (muscle, bone, fat, cartilage, and endothelial
cells), ectoderm (neurons), and endoderm (liver, pancreas, and lung
cells)(Meng et al., 2007; Patel et al., 2008).
Each of these progenitor
cells follow a
different pathway to
become extremely specific blood
cells.
Kathy Niakan and colleagues are providing new understanding of the genes responsible for a crucial change when groups of
cells in the very early embryo first
become organised and set on
different paths of development.
He accomplished that with the help of a virus
different from the retroviruses used initially: an adenovirus that brings the genes into a
cell's nuclear area but doesn't
become part of the
cell's DNA; it disappears after it expresses the reprogramming genes.
The progenitor
cells that those skin
cells become are able to turn into all of the
different cells the newt needs to create a leg.
«Using
different regulators, scientists have been able to induce a subset of myocardial characteristics in various experimental models, but never the complete beating phenotype, so there is something special about gata5 that can take a
cell that's not supposed to
become a heart
cell to actually
become one,» said Stainier.
Transcription factors are expressed (or made) at
different levels in
different cell types, and control what genes are expressed in every
cell, making sure, for example, that a liver
cell remains a liver
cell and does not
become a neuron.
Beverly Emerson studies how
different genes are turned on and off through the course of a cancer — from the time
cells become precancerous until the time they develop into a mature cancer and spread to new organs.
«Learning more about how
different genes cause
cells to
become and remain pluripotent will help us to produce and use stem
cells more reliably.»
«These are interesting results proving it is theoretically possible to «regress»
cells back to an earlier stage in development when they are self - perpetuating and still have the potential to be directed to
become a whole range of
different cell types, whether nerve
cells, heart muscle or bone.
(Adult stem
cells, on the other hand, are much more limited in their potential; they can usually only
become a few
different cell types, and consequently are not applicable for treating as wide a variety of diseases as hESCs are.)
But if, as this study suggests, the way that
cells become proliferative again is similar across many
different organs, we can imagine therapies that interfere with cancer initiation in a more global way, regardless of where that cancer may appear in the body,» he explains.
When a stem
cell divides, it has the potential to either remain as a stem
cell (process known as «self - renewal») or to
become a
different type of
cell with a more specialized function («differentiation»).
The researchers were able to «reprogram» adult skin
cells to
become cells of a
different tissue type.
MSCs hold great potential for the field of regenerative medicine, as they can
become many
different types of
cells (they're «multipotent»), most typically bone, cartilage, and fat
cells.
Immunohistochemical demonstration of Cyclin D1 have
become an important mean for assessing
cell proliferation, therefore the immunohistological demonstration of
cell cycle related antigens such as CDKs which regulated by the
different cyclins could provide a good tool for assessment of cellular proliferation [11].
Willet, Mills, and their colleagues believe the discovery that
cells in
different organs go through the same process to
become proliferative could lead to new potential targets for cancer treatment because the factors that initiate tumours could be the same in multiple organs.
«Although we first
became aware of prions because they cause several bizarre neurological diseases, the discovery that something so awesomely similar happens in organisms as
different as humans and yeast makes us suspect that there is a fundamental, common biochemical process at work here,» said study director Susan Lindquist, PhD, professor of molecular genetics and
cell biology and an investigator in the Howard Hughes Medical Institute at the University of Chicago.
«Bringing together this team, to do this kind of work means we will be better able to understand how stem
cells change as they grow and
become different kinds of
cells.
Researchers used a powerful X-ray microscope at Berkeley Lab's Advanced Light Source (ALS) to capture images of nerve
cell samples at
different stages of maturity as they
became more specialized in their function — this process is known as «differentiation.»
Different factors, including the free radicals that are a byproduct of oxygen metabolism, result in Top1ccs
becoming trapped on DNA and accumulating in
cells.
For example, the same cellular signals that guide early heart development can be used to direct stem
cells to
become the
different heart
cell types needed for modeling disease in a dish.
Although cancer stem
cells have been identified in many
different types of cancer, it is
becoming increasingly clear that the properties of these
cells may vary greatly among the
different tumor types.
However, cancer
cells often invade other tissues where the availability of certain nutrients is drastically
different or grow so quickly that the blood supply, and the accessibility to oxygen and other nutrients that comes with it,
becomes scarce.