Not exact matches
It has become clear that
iPS cells can retain some memories of their previous
state.
The moral complications of the new
state of the art go even deeper, due to an advance that scientists anticipate within a decade: using
iPS cells to create human sperm and egg
cells.
Avoiding the pluripotent
state is important because it avoids the potential danger that «rogue»
iPS cells could develop into a tumor if used to replace or repair damaged organs or tissue.
In a study published in October 2008, Melton showed that it was possible to take an exocrine
cell in the pancreas of a live mouse and turn it into an insulin - producing beta
cell without first going back to an undifferentiated
iPS state.
Rather than reversing
cells all the way back to a stem
cell state before prompting them to turn into something else, such as in the case of
iPS cells, the researchers «rewind» skin
cells just enough to instruct them to form the more than 200
cell types that constitute the human body.
Critical issues include: (i) heterogeneity in stem
cell populations (ii) regulation of
cell fate choices; (iii) declining tissue performance with age and exposure to environmental injuries; (iv) the use of
iPS and Embryonic Stem (ES)
cells, and reprogramming methods for phenotyping disease
states and potential use of these stem
cells in the clinic.
However, while hESCs are created from human embryos,
iPS cells are
cells that were originally from adult tissues, such as skin from an adult body, but have been «reprogrammed» to a hESC - like
state.
All of these data highly support that
iPS cells derived from hNSCs can be reprogrammed to a hESC - like
state at the molecular level.
In light of the observation that
iPS cell derivation takes place under the same culture conditions used for ES
cells [20], we hypothesized that these human feeder
cells could offer a stable tool for defining molecular hallmarks during conversion of differentiated somatic
cells to the pluripotent
state.
Transgenes are inactivated and the endogenous Oct4 promoter is completely demethylated in the established
iPS cell lines, indicating a fully reprogrammed
state.
In addition, their independence of LIF for
iPS cell culture provides an opportunity to further understand the ground
state of ES
cell self - renewal proposed by Ying et al. [21].
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.
In addition, scientists are working to identify the molecules that instruct
iPS cells to adopt a certain
state, which could improve their use for regenerative medicine.
For
cell reprogramming, there are about 2,000 known transcription factors that might be useful in changing a
cell from one
state to another, such as creating induced pluripotent stem (
iPS)
cells from skin
cells.
* Correction: An earlier version of this story incorrectly
stated that Yamanaka did not genetically manipulate the skin
cells used to make
iPS cells in 2006.
By developing a simple chemically defined culture system permitting efficient differentiation of numerous human
iPS cell lines toward
cells of a mature hepatic
state, we now demonstrate the possibility of modeling groups of diseases of non-neuronal origin whose phenotypes are a consequence of complex protein dysregulation within adult
cells.