Vision in low light is dependent on
retinal cells called rods.
Working with researchers at the Friedrich Miescher Institute for Biomedical Research in Switzerland, the MIT team also tested Jaws's ability to restore the light sensitivity of
retinal cells called cones.
Retinitis pigmentosa is an inherited retinal degenerative disease that causes slow but progressive vision loss due to a gradual loss of the light - sensitive
retinal cells called rods and cones.
Working with rats and mice, Xi and colleagues found that specialized
retinal cells called Müller glial cells release IL - 33 in response to retinal injury.
«Overlooked cell key player in preventing age - related vision loss: Tree - shaped
retinal cells called Müller glia may provide a new therapeutic target for treating degenerative eye diseases.»
The retinal cells called cones come in three varieties.
Two of his math professors were collaborating with physiologist Joshua Singer, also at Northwestern, who was keen to model the biology of
a retinal cell called the AII amacrine interneuron.
Not exact matches
From the embryonic stem
cells, the researchers produced a type of tissue
called retinal pigment epithelium (RPE).
A layer of
cells called the
retinal pigment epithelium (RPE) is essential for supporting and nourishing the retina
cells that capture light for vision.
They further demonstrated that the
cells —
called intrinsically photosensitive
retinal ganglion
cells, or ipRGCs — could detect light.
In a developing fetus, she surmised, those phone
calls would reach groups of nerve
cells in the LGN; as their synaptic connections with the
retinal neurons strengthened, the LGN neurons would begin forming «area codes» of their own.
Now, an Australian team reports evidence that the computations take place in
retinal neurons
called ganglion
cells (Science, 29 September, p. 2347).
Next, they used a technique
called fluorescence - activated
cell sorting to separate out the newly differentiated
retinal ganglion
cells from a mixture of different
cells into a highly purified
cell population for study.
In an experimental setup that allowed the two types of
cells to bathe in the same fluid without coming into physical contact,
retinal neurons in a bath with hUTCs formed new connections between neurons
called synapses, and they sprouted new «neurites» — tiny branches that lead to additional connections.
It first targets a protective lining
called the
retinal pigment epithelium (RPE), which shuttles nutrients to the photoreceptor
cells and is vital for their survival.
Scientists have known of the existence of these nerve
cells,
called melanopsin - containing
retinal ganglion
cells (mRGCs), since 2000.
A new gene therapy treatment has restored some sight in a handful of blind patients suffering from Leber's congenital amaurosis, a syndrome in which, because of a broken or missing gene
called RPE65,
retinal photoreceptor
cells malfunction and eventually die.
When these photoreceptors detect light, they send a signal to specialized neurons in the retina
called retinal ganglion
cells, or RGCs, which then transmit visual information to the brain by firing electrical pulses along the optic nerve.
In vertebrates, nerve
cells called retinal ganglion
cells send information from the retina to vision - processing centers in the brain.
That news alone was an exciting breakthrough, but there's more: In lab mice, damaged
retinal ganglion
cells survived longer and were able to regenerate when excess zinc was removed through a chemical process
called chelation.
DHA in brain and
retinal cells also builds reservoirs for molecules
called into action when normal functions are disrupted, resulting in such conditions as
retinal degeneration, Parkinson's or Alzheimer's disease.
Here the so -
called bipolar
cells play a central role, as the first
retinal layer to process the output of the light - sensitive
cells in the eye.
As neuroscientists David Hubel and Torsten Wiesel of Harvard University discovered in a series of groundbreaking experiments in the 1960s, individual
cells in the visual cortex, so -
called binocular
cells, receive input from both eyes, specifically from corresponding
retinal locations, thus providing a mechanism for perceptual fusion.
First, researchers found a pigment
called melanopsin in a small subset of
retinal ganglion
cells (RGCs) in the eyes of rats.
The technique developed is
called DARC, which stands for detection of apoptosing
retinal cells.
In research published this week in the Journal of Neuroscience, University at Buffalo scientists and colleagues focused on a particular protein,
called a transcription factor, that regulates gene activity necessary for the development of one type of
retinal neuron, the horizontal
cells.
As you mentioned, in dry AMD we basically have atrophy in the back of the retina in
cells that are
called retinal pigment epithelial
cells.
What we discovered was that was in fact there are a certain group of
cells in the retina,
retinal ganglion
cells, and a particular group of those ganglion
cells which we
call OFF
cells.
In addition to differentiated
retinal cells, the amphibian eye contains a population of self - renewing
retinal stem
cells located in the
retinal periphery in a region
called the ciliary marginal zone or CMZ.
We hypothesize that upon
retinal neuronal damage MG or RPE
cells undergo defined and controlled changes in cellular and molecular phenotype towards a
cell with progenitor properties — this process that we are studying we
call regenerative reprogramming.
Those are understandably
called the «on»
retinal ganglion
cells and «off»
retinal ganglion
called.
Behind the photoreceptors is another layer of
cells called retinal pigment epithelium (RPE), which support the rods and cones by delivering nutrients from the bloodstream and removing waste that the rods and cones generate.
The treatment could help people who have a fault in a gene
called RPE65, which causes problems in the
retinal pigment epithelium (RPE), a thin layer of
cells that support and nourish photoreceptors.
The researchers wanted to understand how
retinal cells survive the initial vascular damage, and found that they go into a self - preservation mode
called senescence.
Eventually the paintings emerge, but the little bubbles, as we
call them, are stimulating specific types of
retinal ganglion
cells in very specific ways, which is necessary, we know from other studies, to encourage their ongoing health by transmitting electrical signals down their axons to the brain.
The stem
cell approach I am most excited about involves a treatment to replace
cells called retinal pigment epithelial
cells.
The
retinal cells that help us see in bright light are
called cones, and these are not destroyed by the disease itself, but by the toxic by - products released by the rod
cells as they die.