More forward looking statements (without any of the standard legalese on risks, assumptions and uncertainty) regarding the great mystery of embryonic stem cells maybe, sort of, perhaps, soon to give up it’s secrets.
So what’s the deal?
“Pluripotency is defined as the capacity of individual cells to initiate all lineages of the mature organism in response to signals from the embryo or cell culture environment.”1
Embryonic stem cells have pluripotency. Discovery of the methods and aspects which allow for pluripotency in embryonic stem cells are definitely a research milestone and one which will advance many lines of inquiry in various fields of medicine…but…there are a few major issues, particularly in the USA.
- There are already ADULT stem cells which ARE PLURIPOTENT and can be used for treatment.
- The US is in a bitter tug of war in both accurate media coverage of stem cells and research and use of adult versus embryonic stem cells.
- Pharma is trying to make drugs out of this stuff and get patents on it.
- In most cases, your own body can supply the necessary stem cells for your own treatment.
- And of course, the controversy issues of utilizing embryonic stem cells which will cause the religious right to exert huge resistance on any advancement of embryonic stem cell research in the US.
While the US is still playing a game of catch up in adult and embryonic research and especially treatment; please remember, embryonic stem cell research was fully funded with government backing in many countries around the world for over a decade resulting in…
ZERO EMBRYONIC STEM CELL TREATMENTS.
So don’t get your hopes up for embryonic treatment anytime soon, but then again,
ADULT stem cells are here, now, powerful, safe and effective. What are you waiting for?
Mechanisms That Allow Embryonic Stem Cells to Become Any Cell in the Human Body Identified
ScienceDaily (July 18, 2012) — New research at the Hebrew University of Jerusalem sheds light on pluripotency — the ability of embryonic stem cells to renew themselves indefinitely and to differentiate into all types of mature cells. Solving this problem, which is a major challenge in modern biology, could expedite the use of embryonic stem cells in cell therapy and regenerative medicine.
If scientists can replicate the mechanisms that make pluripotency possible, they could create cells in the laboratory which could be implanted in humans to cure diseases characterized by cell death, such as Alzheimer’s, Parkinson’s, diabetes and other degenerative diseases.
To shed light on these processes, researchers in the lab of Dr. Eran Meshorer, in the Department of Genetics at the Hebrew University’s Alexander Silberman Institute of Life Sciences, are combining molecular, microscopic and genomic approaches. Meshorer’s team is focusing on epigenetic pathways — which cause biological changes without a corresponding change in the DNA sequence — that are specific to embryonic stem cells.
The molecular basis for epigenetic mechanisms is chromatin, which is comprised of a cell’s DNA and structural and regulatory proteins. In groundbreaking research performed by Shai Melcer, a PhD student in the Meshorer lab, the mechanisms which support an “open” chromatin conformation in embryonic stem cells were examined. The researchers found that chromatin is less condensed in embryonic stem cells, allowing them the flexibility or “functional plasticity” to turn into any kind of cell.
A distinct pattern of chemical modifications of chromatin structural proteins (referred to as the acetylation and methylation of histones) enables a looser chromatin configuration in embryonic stem cells. During the early stages of differentiation, this pattern changes to facilitate chromatin compaction.
But even more interestingly, the authors found that a nuclear lamina protein, lamin A, is also a part of the secret. In all differentiated cell types, lamin A binds compacted domains of chromatin and anchors them to the cell’s nuclear envelope. Lamin A is absent from embryonic stem cells and this may enable the freer, more dynamic chromatin state in the cell nucleus. The authors believe that chromatin plasticity is tantamount to functional plasticity since chromatin is made up of DNA that includes all genes and codes for all proteins in any living cell. Understanding the mechanisms that regulate chromatin function will enable intelligent manipulations of embryonic stem cells in the future.
“If we can apply this new understanding about the mechanisms that give embryonic stem cells their plasticity, then we can increase or decrease the dynamics of the proteins that bind DNA and thereby increase or decrease the cells’ differentiation potential,” concludes Dr. Meshorer. “This could expedite the use of embryonic stem cells in cell therapy and regenerative medicine, by enabling the creation of cells in the laboratory which could be implanted in humans to cure diseases characterized by cell death, such as Alzheimer’s, Parkinson’s, diabetes and other degenerative diseases.”