THIS IS ONLY FOR INFORMATION, ALWAYS CONSULT YOU PHYSICIAN BEFORE HAVING ANY PARTICULAR FOOD/ MEDICATION/EXERCISE/OTHER REMEDIES. PS- THOSE INTERESTED IN RECIPES ARE FREE TO VIEW MY BLOG- https://gseasyrecipes.blogspot.com/ FOR INFO ABOUT KNEE REPLACEMENT, YOU CAN VIEW MY BLOG- https:// kneereplacement-stickclub.blogspot.com/ FOR CROCHET DESIGNS Scientists neutralize and reverse a key genetic risk factor for Alzheimer's
Alzheimer's disease has a range of risk factors, but one of the clearest connections is the gene apoE4.
Now, researchers have peered closer at the
protein encoded by this gene and uncovered how it affects the brain, how
it increases the risks of Alzheimer's and most importantly, how the
damage can be reversed.
The apoE gene
comes in three variations, apoE2, E3 and E4, and everybody carries two
copies in various combinations. The most common form is apoE3, and it
doesn't seem to have any influence over a person's likelihood of
developing Alzheimer's. But apoE4, present in up to 15 percent of
people, is the real troublemaker: Having one copy increases the
Alzheimer's risk by two to three times, while those unlucky enough to
have two copies are 12 times more likely to develop the disease.
But why is that the case? The
proteins created by these genes are extremely similar, with apoE4
differing from apoE3 at only one tiny point. So, the new study set out
to examine what problems the former is causing in the brain, and whether
that single change can be canceled out.
Rather than using mouse
models, the results of which don't usually translate well to human
biology, the researchers experimented with human cells
instead. The team gathered skin cells from Alzheimer's patients with two
apoE4 genes, as well as some from people with two apoE3 genes without
Alzheimer's. These were converted into induced pluripotent stem cells,
and then turned into human neurons.
The team compared the
neurons from the apoE3 and apoE4 donors, and found that the latter
didn't function as well as they should. This means the protein breaks
down into fragments in the cells, over time leading to the build-up of
proteins in the brain that forms the calling card of Alzheimer's.
Interestingly, apoE4's
devastating effects are clear in humans but not in mice. That
illustrates the flaws in using animal models of human diseases, and may
go a long way towards explaining why treatments that previously seemed
so promising in mice haven't panned out in human trials.
"There's an important species
difference in the effect of apoE4 on amyloid beta," says the first author of the study. "Increased amyloid beta production is
not seen in mouse neurons and could potentially explain some of the
discrepancies between mice and humans regarding drug efficacy. This will
be very important information for future drug development."
Having determined that
apoE4 damages human brain cells, the team wanted to examine the root of
the problem – namely, whether the problems were caused by the presence
of apoE4 or perhaps just the absence of apoE3.
"It's
fundamentally important to address this question because it changes how
you treat the problem," says the lead author of the study.
"If the damage is caused due to the loss of a protein's function, you
would want to increase protein levels to supplement those functions. But
if the accumulation of a protein leads to a toxic function, you want to
lower production of the protein to block its detrimental effect."
To figure that out, the team
grew brain cells with no forms of apoE, and found they functioned much
the same as those with the common apoE3 protein. As soon as apoE4 was
added though, the neurons degraded in a familiar Alzheimer's fashion,
indicating that this protein is actively the problem.
Best of all, the researchers
were able to fix the damage after the fact, using a class of compounds
that turn apoE4 into something closer to E3. Treating the brain cells
with these structure-correcting molecules restored function to the
neurons, and effectively reversed the signs of Alzheimer's. The
scientists are now looking to the pharmaceutical industry to help with
improving the compounds for future testing in human patients.
THIS IS ONLY FOR INFORMATION, ALWAYS CONSULT YOU PHYSICIAN BEFORE HAVING ANY PARTICULAR FOOD/ MEDICATION/EXERCISE/OTHER REMEDIES. PS- THOSE INTERESTED IN RECIPES ARE FREE TO VIEW MY BLOG- https://gseasyrecipes.blogspot.com/
FOR INFO ABOUT KNEE REPLACEMENT, YOU CAN VIEW MY BLOG- https:// kneereplacement-stickclub.blogspot.com/
FOR CROCHET DESIGNS https://my crochet creations.blogspot.com/
THIS IS ONLY FOR INFORMATION, ALWAYS CONSULT YOU PHYSICIAN BEFORE HAVING ANY PARTICULAR FOOD/ MEDICATION/EXERCISE/OTHER REMEDIES. PS- THOSE INTERESTED IN RECIPES ARE FREE TO VIEW MY BLOG- https://gseasyrecipes.blogspot.com/
FOR INFO ABOUT KNEE REPLACEMENT, YOU CAN VIEW MY BLOG- https:// kneereplacement-stickclub.blogspot.com/
FOR CROCHET DESIGNS https://my crochet creations.blogspot.com/
Labels: accumulation, Alzheimer's, amyloid beta, gene apoE4, human neurons, pluripotent stem cells (PSCs), protein, toxic functions
0 Comments:
Post a Comment
<< Home