SAN FRANCISCO, CA — April 9, 2018 —
Using human brain cells, scientists at the Gladstone Institutes discovered the cause of — and a potential solution for — the primary genetic risk factor for Alzheimer's disease, a gene called apoE4.
Not exact matches
This technique has been
used, as Arnold reports, to trace the progress of cancers, advance our understanding of obesity and diabetes, and prove that
brain cells continue to form through a
human being's lifetime.
Using a mathematical model known as the Ising model, invented to describe phase transitions in statistical physics, such as how a substance changes from liquid to gas, the Johns Hopkins researchers calculated the probability distribution of methylation along the genome in several different
human cell types, including normal and cancerous colon, lung and liver
cells, as well as
brain, skin, blood and embryonic stem
cells.
In a
human brain, 85 billion nerve
cells communicate via trillions of connections
using complex patterns of electrical jolts and more than 100 different chemicals.
Using human fetal «mini-brains» grown in 3 - D cultures, scientists determined that a specific protein produced by the Zika virus changes the properties of neural stem
cells in the developing
brain of an infected fetus, potentially causing microcephaly in newborns (Ki - Jun Yoon, abstract 103.06, see attached summary).
Researchers in optogenetics can control genetically modified
brain cells using light but because of these modifications, the technique is not yet deemed safe to
use in
humans.
A technique that involves genetically engineering
brain cells so that they fire in the presence of certain drugs has been
used to treat epilepsy in rats, and it could soon be tested in
humans.
While mouse models have traditionally been
used in studying the genetic disorder, Deng said the animal model is inadequate because the
human brain is more complicated, and much of that complexity arises from astroglia
cells, the star - shaped
cells that play an important role in the physical structure of the
brain as well as in the transmission of nerve impulses.
Scientists can't yet grow spare parts of the
human brain to fix neurological injuries or defects, but they have recently
used stem
cells to create
brain organoids, formations of
cells that mimic some of the
brain's regions.
Within a decade, we should be able to
use these technologies to read and alter the state of neurons for an enormous fraction of the
cells in
human brains.
The team
used human embryonic stem
cells — which can transform into any
cell of the body — and cultured them in a mixture of chemicals to grow
human brain cells.
For his part, Collins, who has led NIH since 2009 and been kept on by the Trump administration, pointed to an array of promising NIH activities, including the development of new technologies to provide insights into
human brain circuitry and function through the Brain Research through Advancing Innovative Neuroethologies (BRAIN initiative) and the use of the gene - editing tool CRISPR - Cas9 to correct mutations and clear the way to develop and test a «curative therapy» for the first molecular disease: sickle cell dis
brain circuitry and function through the Brain Research through Advancing Innovative Neuroethologies (BRAIN initiative) and the use of the gene - editing tool CRISPR - Cas9 to correct mutations and clear the way to develop and test a «curative therapy» for the first molecular disease: sickle cell dis
brain circuitry and function through the
Brain Research through Advancing Innovative Neuroethologies (BRAIN initiative) and the use of the gene - editing tool CRISPR - Cas9 to correct mutations and clear the way to develop and test a «curative therapy» for the first molecular disease: sickle cell dis
Brain Research through Advancing Innovative Neuroethologies (BRAIN initiative) and the use of the gene - editing tool CRISPR - Cas9 to correct mutations and clear the way to develop and test a «curative therapy» for the first molecular disease: sickle cell dis
Brain Research through Advancing Innovative Neuroethologies (
BRAIN initiative) and the use of the gene - editing tool CRISPR - Cas9 to correct mutations and clear the way to develop and test a «curative therapy» for the first molecular disease: sickle cell dis
BRAIN initiative) and the use of the gene - editing tool CRISPR - Cas9 to correct mutations and clear the way to develop and test a «curative therapy» for the first molecular disease: sickle cell dis
BRAIN initiative) and the
use of the gene - editing tool CRISPR - Cas9 to correct mutations and clear the way to develop and test a «curative therapy» for the first molecular disease: sickle
cell disease.
Using an in vitro
human blood
brain barrier model, the researchers demonstrated that radiolabeled mAb2556 could cross the blood
brain barrier and kill HIV - infected
cells without any overt damage to the barrier itself.
• Fred Gage and his colleagues at the Salk Institute in La Jolla, California, harvested
brain cells from
human cadavers and
used them to form neural progenitor
cells, precursors to adult
human brain cells.
«The novelty of this study is two-fold: We
used a preclinical prevention paradigm of a CRF - antagonist (a drug that blocks the CRF receptor in
brain cells) called R121919 in a well - established AD model — and we did so in a way that draws upon our experience in
human trials.
Even better than the real thing, the NIST synapse can fire much faster than the
human brain — 1 billion times per second, compared to a
brain cell's 50 times per second —
using just a whiff of energy, about one ten - thousandth as much as a
human synapse.
To replicate these
cell culture results, Rani
used human stem
cells to grow neurons into what is called a mini
brain.
In researches
using the more complex animals, it is known that certain nerve
cells in the
brain integrate information and make a decision when reaching a certain level, which likely occurs also in
humans.
The scientists
used the new indexing method on several
human cell lines and from a mouse
brain to reveal the methylome of 3,282 single
cells.
A technique that involves genetically engineering
brain cells so that they fire in the presence of certain drugs has been
used to treat an epilepsy - like condition in rats, and it could soon be trialled in
humans.
Linking the amount of carbon - 14 found in organic material with the bomb curve has been
used to date
human tooth enamel and even regenerating
brain cells.
Investigations into
human brain development
using human cells in the culture dish have so far been very limited: the
cells in the dish grow flat, so they do not display any three - dimensional structure.
I mean, it is as I think everybody in this audience knows the old dogma
used to be that adult
humans, like all adult mammals, we didn't generate new
brain cells.
Using a 3D, stem
cell - based model of a first - trimester
human brain, the team discovered that Zika activates TLR3, a molecule
human cells normally
use to defend against invading viruses.
THE gene - editing technique CRISPR has been
used in the lab to switch on a gene in
human brain cells whose dormancy is behind a learning disability.
In tests
using human neural progenitor
cells (NPCs)-- self - renewing, multipotent
cells that generate neurons and other
brain cell types — the scientists found that exposure to sofosbuvir not only rescued dying NPCs infected with the Zika virus, but restored gene expression linked to their antiviral response.
Past clinical trials of stem
cell therapies for chronic stroke patients
used cells derived from tumors in
humans and
brain tissue from fetal pigs.
That's because most studies on single
human brain cells use dead rather than living tissue, and many others rely on
cells from common laboratory animals, especially mice.
«The key breakthrough came from
using a fruit fly model of
human ALS and FTD that allowed us to screen these 400 candidates for ones that block
brain cell death in a living organism,» says Lloyd.
They
used the forebrain, the first mini-
brain with the six layers of
brain cell types found in the
human cortex, for the current study on Zika.
Dr. Sonntag studies this concept on the molecular and cellular level
using a translational research approach that integrates the analysis of
human material, such as postmortem
brains, primary
cell systems, and neural
cell populations generated from patients» - or healthy individuals» - derived induced pluripotent stem
cells (iPSC), or induced neurons (iNs), in combination with molecular, biochemistry, and lentivirus - mediated gene - engineering technologies.
UC San Francisco researchers have identified
cells» unique features within the developing
human brain,
using the latest technologies for analyzing gene activity in individual
cells, and have demonstrated that large - scale
cell surveys can be done much more efficiently and cheaply than was previously thought possible.
Gladstone scientist Dr. Sheng Ding has exposed more chameleon - like qualities of the
human skin
cell,
using chemical cocktails to turn skin
cells into fully functional
brain, heart, liver, and insulin - producing pancreas
cells.
«We expect to
use this approach to help us better understand how the complexity of the
human cortex arises from
cells that are spun off through
cell division from stem
cells in the germinal region of the
brain.»
The advantages of this approach began to emerge in 2011, when Dr. Ding announced that he had
used his «chemical reprogramming» method to convert
human skin
cells into
brain cells.
Strengthening the link between Zika virus and microcephaly, scientists at UC San Francisco have discovered that a protein the virus
uses to infect skin
cells and cause a rash is present also in stem
cells of the developing
human brain and retina.
Gage's team
used human pluripotent stem
cells to develop
brain organoids, which were grown in culture for 40 to 50 days.
The team
used genetically engineered mice to study the effects of different
human apoE variants on the maturation of neural stem
cells or progenitor
cells, from which new neurons develop in the adult
brain.
The
Human Connectome Project, which is an international effort to map the connectomes of 1,000 people on a macro scale — mostly just the white matter, or active myelinated (insulated) nerve
cell bundles —
using magnetic resonance imaging, this week announced its finding that
brain wiring patterns correlate with behavioral and demographic traits.
Their work will
use heart
cells from animals, and
brain and heart
cells made from
human «adult» stem
cells.
We are
using a new technique, called single
cell RNA sequencing, to isolate thousands of single neurons from
human brain tissue, study all the genes that are expressed in each individual
cell, and make
cell - to -
cell comparisons between normal, early stage and late stage AD.
The mini
brains are derived from
human stem
cells thus, may be
used instead of animal models to test new drugs, revolutionizing the way lab experiments work.
«We kept them healthy, and without giving them many instructions on what kind of
cells they should become they produced many of the
cells present in the
human brain and achieved the formation of complex tissue,» says Arlotta, describing the
brain organoids she
used in research published in Nature in May 2017.
Extensive
use is made of our
human brain bank and our stock of
human cell lines.
Human skin
cells have also been directly converted into neurons that can be
used to study and find treatments for diseases in the
brain, as well as liver
cells and insulin - producing
cells of the pancreas.
And on Feb. 24, Reuters reported that California scientists had
used human stem
cells to create
human neurons in mouse
brains.
Now, Salk Institute scientists studying roundworms suggest that, in both worms and
humans, adolescent
brains mature to stable adult
brains by changing which
brain cells they
use to generate behavior.
Now, scientists at the Salk Institute have studied a 3D «mini-brain» grown from
human stem
cells and found it to be structurally and functionally more similar to real
brains than the 2D models in widespread
use.
Supported by a CIRM translational grant, scientists in Huang's laboratory are
using human stem
cells to create inhibitory neuron progenitors — early - stage
brain cells that can develop into mature inhibitory neurons.
Using a mouse model for this disease, which in
humans involves the destruction of white matter in the
brain, a research team led by Albee Messing, director of the UW — Madison Waisman Center, found that a protein behind the symptoms of the disease, called GFAP, is broken down more rapidly in the body than researchers previously found in
cell culture studies.