People already have ways to put
proteins into brain cells.
Not exact matches
The results could provide insights
into the Zika virus» recent emergence as a global health emergency, and also point to inhibitors of the
protein p53 as potential leads for drugs that could protect
brain cells from
cell death.
Brain cells translate that genomic gobbledygook
into rogue
proteins, which do bad things inside nerve
cells and eventually trigger symptoms, such as involuntary movements.
When injected
into mice engineered with a tau mutation that makes the
protein clump abnormally in
brain cells, triggering memory and motor problems, the antibodies reduced the clumping and improved the animals» behavior.
The researchers have now provided further evidence for this new theory by showing that the abnormal
protein coded for this genetic disorder can be transmitted to normal animals by the injection of diseased
cells into their
brain.
Published in the February 27 issue of
Cell, the study found that tumor
cells that reach the
brain — and successfully grow
into new tumors — hug capillaries and express specific
proteins that overcome the
brain's natural defense against metastatic invasion.
Svendsen injected
into their
brains a
protein known to enhance neural development, called glial
cell line - derived neurotrophic factor (GDNF).
As Pardridge studied the
protein more carefully, he realized that it transports essential insulin
into the
cell and then out the other side, from which point the hormone travels
into the
brain to help regulate eating behavior.
The first step in the process involves inserting
into those
brain cells a gene that makes a light - sensitive
protein.
The
cells that make up the walls of blood capillaries are joined together more tightly in the
brain than elsewhere in the body, preventing
proteins and
cells getting
into the
brain.
«The blood -
brain barrier is chemically tight because the
cells contain transporter
proteins which make sure that substances entering the
cells are thrown straight back out
into the bloodstream again.
They found that when fibrinogen (a blood - clotting
protein) leaks
into the central nervous system, it stops
brain cells from producing myelin and, as a result, prevents repair.
One of the genes involved in feeding the big
brain, called SLC2A1, builds a
protein for transporting glucose from blood vessels
into cells.
The retina sits at the back of the human eye, and contains
protein cells that convert light
into electrical signals that travel through the nervous system, triggering a response from the
brain, ultimately building a picture of the scene being viewed.
Originally from algae, the gene makes a
protein called channelrhodopsin - 2, which reacts to blue light by admitting ions
into the
brain cells, activating them in the process.
THE GREAT DIVIDE Young
brain stem
cells (one shown dividing, left) pack old
proteins tagged with ubiquitin (red)
into one daughter
cell.
When they stripped the vesicles of
protein and their genetic cargo and injected them back
into mice, the blood
cells no longer went to the site of
brain injury.
Still, when the
brain cells and spinal cord
cells of these babies were examined at autopsy, there was clear evidence that nusinersen had tricked SMN2
into producing a great deal more of the full length, motor neuron - protecting
protein: two to six times more copies of SMN's messenger RNA were found in spinal cord samples from nusinersen - treated babies than in autopsy samples from untreated infants.
Mouse embryonic stem
cells injected
into rat
brains express the AHD2
protein marker (yellow) characteristic of
cells lost in Parkinson's disease.
Methylmercury crosses the protective blood -
brain barrier by binding with an essential amino acid that has dedicated carrier
proteins for shunting it
into brain cells.
In studies of neural development in mice, Stahl found that TRNP1 produces a
protein that determines whether neural stem
cells self - replicate, leading to a balloonlike expansion of cortical surface area, or whether they differentiate
into a plethora of intermediate stem
cell types and neurons, thickening the cortex and forming more complex
brain structures.
In Alzheimer's, this
protein — present in all healthy
brains — can accumulate and clump, developing
into cell - damaging plaque.
«This data allows classification of all human
protein - coding genes
into those coding for house - hold functions (present in all
cells) and those that are tissue - specific genes with highly specialized expression in particular organs and tissues, such as kidney, liver,
brain, heart, pancreas.
A cellular
protein called PAK1 stimulates the growth of dendritic spines, or protrusions, that allow communication between neurons, and Roy had a hunch that this
protein — when transported
into brain cells — might help bring silent engrams back
into direct awareness.
The
protein tau is normally found in
brain cells, but scientists don't know why it clumps
into tangles in people with Alzheimer's disease.
«Importantly, this analysis helped us identify the
protein fibrinogen as the key culprit in MS, by demonstrating how its entry
into the
brain through leaky blood vessels impacted the health of individual nerve
cells.»
From there, the ASOs get taken up
into brain cells where they continue to suppress their target
protein for a month or so, after which time more needs to be injected.
An intricate new three - dimensional
protein structure is providing a detailed look
into how
brain cells communicate rapidly.
Bone marrow stem
cells are recruited by GCSF to go
into the
brain and take away the harmful beta - amyloid
protein which starts Alzheimer's.
Brain cells pick up the labeled leucine over the course of hours and it's incorporated
into new copies of amyloid - beta and other
proteins they make.
It hides in tofu dogs under aliases such as textured vegetable
protein, hydrolyzed vegetable
protein, and lecithin — which is troubling, since the processing required to hydrolyze soy
protein into vegetable
protein produces excitotoxins such as glutamate (think MSG) and aspartate (a component of aspartame), which cause
brain -
cell death.