The pathway that it takes decides in which valley it will finally settle, providing a metaphor for the acquisition of
a specific cell fate.
These workers considered that this fluctuation might account for reversible lineage priming towards
specific cell fates.
Not exact matches
The two - part approach netted a set of mutations seen only at relapse that enabled the team to sift and sort leukemic and normal stem
cells using tools developed in the Dick lab a few years ago to zero in on
specific cell types
fated to relapse.
By monitoring stem
cell differentiation on gels that mimic the stiffness and nanofibrous structure of biological tissue, researchers have identified the
specific molecules that stem
cells use when selecting bone and cartilage
fates.
Her research team placed the evolutionarily conserved castor (Cas) gene, which encodes a zinc finger protein, in a genetic circuit with two other evolutionarily conserved genes, hedgehog (Hh) and eyes absent (Eya), to determine the
fates of
specific cell progeny (daughters).
The expression of
specific genes in a particular root
cell determine its
fate — the zone in which it will function, Subramanian explained, so he is identifying which micro-RNAs direct gene expression to achieve this differentiation.
It will be interesting to determine if
specific EFTF subsets can
fate pluripotent
cells to other (nonretinal) neural lineages.
Each
cell fate is characterized by a regulatory network of factors, typically transcription factors that maintain a
specific state through reciprocal feedback interactions.
A better understanding of this master switch regulator may help to understand, how
cells that have a common origin take on a
specific fate in the body to build an organ and may also help to understand the development of certain leukemias.
Found that muscle -
specific histone methyltransferases and microRNAs regulate the activity of Hand2, a transcription factor essential for ventricle formation and more recently showed that microRNAs can efficiently guide stem
cell fate decisions.
In doing so,
specific cell types may activate immune responses to fine tune
cell -
fate decisions at the organismal level; for instance, DNA damage in germ
cells induces an innate immune response in worms that promotes endurance of somatic tissues to allow delay of progeny production when germ
cells are hit by DNA damage.
Because the embryo is transparent it is possible to use fluorescent proteins to label
specific cells and their components, and then use this to watch the
fate of the
cells in the presence or absence of different genes.
Both human embryonic stem
cells (hESC) and induced pluripotent stem
cells (iPSC) can colonize the mouse embryo in a manner predicted from classical developmental
fate mapping and faithfully recapitulate tissue -
specific fate post-transplantation.
Our findings suggest that pluripotency is determined by the capacity of a mixed population of lineage - biased intermediates to commit to different
cell fates in
specific contexts.