Women with
Alzheimer’s live longer than men with the disease, and scientists at UC San
Francisco now have evidence from research in both humans and mice that this is
because they have genetic protection from the ravages of the disease.
By virtue of having a second X chromosome, women get
two “doses” of a protective protein from a gene that only exists on this female
sex chromosome. Some people, both male and female, have an especially potent
variant of this gene, which is called KDM6A, that gives them even more
protection. But, because of the way sex chromosomes work — women have two X’s,
but men only have one — women have two copies of this gene churning out the
protective protein.
The new study offers a first look at how sex
chromosomes affect vulnerability to Alzheimer’s. And it helps explain why women
survive longer and with less severe symptoms than men during early stages of
the disease, even when they have comparable levels of toxic Alzheimer’s
proteins in their brains.
“This finding challenges a long-standing dogma that
women are more vulnerable to Alzheimer’s,” said Dena Dubal, MD, PhD, associate
professor of neurology at UCSF and senior author of the study, published August
26, 2020, in Science Translational Medicine. Dubal is the David
Coulter Endowed Chair in Aging and Neurodegenerative Disease, and a member of
the UCSF Weill Institute for Neurosciences. “More women than men have
Alzheimer’s because they survive to older ages, when risk is highest. But they
also survive with the disease for longer.”
While much of a female’s second X chromosome is
“silenced” by an outer layer of non-coding RNA, a small number of genes escape
this process, in both mice and humans, giving females twice the dose of the
proteins coded for by those genes. The researchers zeroed in on one of these
active genes, KDM6A, which is already known to be involved in learning and
cognition: when this gene malfunctions, it causes Kabuki syndrome,
characterized by developmental delay and mild to severe intellectual
disability.
Combing through public databases of gene expression
studies, the scientists discovered an especially active variant of KDM6A that
is carried by about 13 percent of women and 7 percent of men around the world.
Because women have two X chromosomes, they have a greater chance of carrying at
least one copy of this variant, and some women carry two copies.
When the scientists looked at several long-term
studies of older people, many of whom already had mild cognitive impairment,
they could see that women with one copy — or even better, two copies — of the
variant appeared to progress more slowly toward Alzheimer’s. It’s not yet clear
if the same holds true for men who carry the variant on their X chromosome,
since there may have been too few of them in the study to see any effects.
Little is known about the ways that genetics drive
differences in how diseases affect men and women, said Jennifer Yokoyama, PhD,
an associate professor of neurology at the UCSF Memory and Aging Center and
member of the Weill Institute, who analyzed the KDM6A variant in the new study.
“Because the X and Y chromosomes are hard to compare to one another, the big
genome-wide association studies have all been done on non-sex chromosomes,”
Yokoyama said. “Perhaps our study will highlight the fact that there could be
something pretty interesting on the X chromosome after all.”
The gene expression studies showed that women in
general had more KDM6A protein in their brains than men. They also showed that
people with Alzheimer’s had more of the protein in brain regions that get
damaged early in the disease. The researchers theorized that neurons in these
regions may produce more of the protein to protect against the disease,
although the data they analyzed could only identify associations, and not prove
causes.
To get closer to this causal question, the scientists
performed experiments in mice. First, they looked inside the brains of female
mice and confirmed that both copies of Kdm6a were actively transcribing RNA to
make protein. Female mice had significantly higher levels of this protein in a
brain region called the hippocampus, which is critical to learning and memory
and gets damaged early in Alzheimer’s.
Then they bred mice which model human Alzheimer’s by
producing toxic amyloid beta in their brains, so their male offspring produced
amyloid and also carried two X chromosomes like females.
With a second X chromosome, the male mice did better
on cognitive tests, and they also lived longer, despite the toxic proteins in
their brains. To be sure it was the second X that provided protection, rather
than the absence of a Y chromosome, scientists deleted the second X from female
Alzheimer’s mice. And just like males, these female mice were more cognitively
impaired and died faster.
In further tests, when the scientists exposed neurons
from male and female mouse brains to increasing doses of amyloid beta, the male
neurons died faster. But this difference was eliminated when the scientists
used a gene editing technique to reduce Kdm6a protein levels in the neurons
from females’ brains and increased it in the neurons from male mouse brains.
The researchers built on these findings by increasing
Kdm6a in a region of the hippocampus called the dentate gyrus, which is
involved in spatial learning and memory, in male Alzheimer’s mice. One month
later, the male mice had as much of the gene’s protein in that brain region as
the female mice. These males also did significantly better on tests of spatial
memory than male mice without the added Kdm6a.
“Our study reveals a new role for sex chromosomes,”
Dubal said. “This protective mechanism on the X chromosome opens the
possibility that we could increase resilience to Alzheimer’s and other
neurodegenerative disorders by boosting Kdm6a or other X factors in both men
and women.”
Source: https://www.ucsf.edu/news/2020/08/418291/female-chromosomes-offer-resilience-alzheimers
Journal article: https://stm.sciencemag.org/content/12/558/eaaz5677
Source: https://myfusimotors.com/2020/09/27/female-chromosomes-offer-resilience-to-alzheimers/
No comments:
Post a Comment