(A) Extensive preservation of the nuclear
photoreceptor layers in the dorsal retina of the dystrophic RCS rat 13 weeks following transplantation of iPS - RPE cells (DAPI stained nuclei).
Remember the retina is
the photoreceptor layer of the eye, which is responsible for converting visual images to electrical signals.
Not exact matches
Missing from the eye was the
layer of rods and cones, the
photoreceptors that catch light.
Light enters through the pupil and passes through four
layers in the retina before reaching the light - sensitive
photoreceptors.
The retinal pigment epithelium (RPE) is a single
layer of cells that accomplishes multiple functions, such as providing survival molecules that prevent
photoreceptors from dying.
The second
layer is made of bipolar cells that act as a conduit between the
photoreceptor and the third type of cell, the ganglion, which transmits the light signals to the brain.
The first
layer contains the
photoreceptors — the rods and cones that detect light.
Some of the cells in this
layer (the
photoreceptors) convert light into an electrical signal that is then amplified and processed by other cells before being sent to the brain via the optic nerve.
However, the direction of motion is not explicitly represented at the level of the
photoreceptors but rather must be calculated by subsequent
layers of nerve cells.
This implant makes use of bipolar cells, as these form the second
layer downstream of
photoreceptor cells lost to the progress of disease.
The black
layer on top of the
photoreceptors is retinal pigment epithelium.
In wild - type, retinal ganglion cell
layer (GCL), inner nuclear
layer (INL), inner plexiform
layer (IPL), and nuclear
layers of rod and cone
photoreceptors are distinct, and rod outer segment (OS) is observed at the outer-most
layer of the retina.
Typically, when light passes through the transparent tissue of the retina and strikes
photoreceptors, they initiate electrochemical signals that propagate forward through a
layer of bipolar cells to ganglion cells.
In Figure 5O, the number of rod
photoreceptor, inner nuclear
layer, and retinal ganglion cells were determined by counting the nuclei of cells expressing XAP2, Calretinin, or in the RGC
layer, respectively.
(A) Rosettes (arrowheads) and pseudo outer nuclear
layers (arrow) are detected in explants triple stained for nuclei (blue; DAPI), cone (green; Calbindin), and rod
photoreceptors (red; XAP2).
When transplanted to the subretinal space of mice lacking functional
photoreceptors, human embryonic stem cells directed toward a retinal lineage integrate into the outer nuclear
layer, express
photoreceptor markers, and restore a light response as determined by the electroretinogram (ERG)[5].
Calretinin - expressing (likely bipolar) cells were also observed extending processes toward the peduncles of nearby
layered photoreceptors (Figure 7C).
The retinal pigment epithelium (RPE) is a
layer of cells next to the retina that are metabolically coupled to the retina's
photoreceptor neurons.
The RPE is a single
layer of cells lining the back of the retina that is vital to the functioning of the retinal
photoreceptor cells, and thus vision itself.
If the
layer is not sustained, which the implant intends to replace, then the
photoreceptor cells also die off, and people lose their sight slowly as a result.
A population of these cells forms a
layer deep to the
photoreceptors, where they contain intracellular pigment granules and appear superficially like an extra RPE
layer, even though they do not express at least two characteristic RPE proteins.
Photoreceptor inner segments (IS) are visible above the pigmented donor cell layer, demonstrating partial preservation of photorecept
Photoreceptor inner segments (IS) are visible above the pigmented donor cell
layer, demonstrating partial preservation of
photoreceptorphotoreceptor structure.
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.
(E) Low power view of a retina section obtained from the same eye used in panel A showing extensive rescue of
photoreceptors within the outer nuclear
layer (ONL) after subretinal injection of hNPCctx — GDNF.
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.
Light travels through the eyeball to reach the retina, then passes through several transparent
layers of cells to strike the rod - and cone - shaped
photoreceptor cells.
Both unmodified and genetically modified groups were found to have cells that migrated and survived in two distinct locations: (i) as a separate, nearly continuous, subretinal
layer lying between the host RPE and
photoreceptors, and (ii) as individual cells distributed throughout the neurosensory retina, especially within the inner retinal
layers (Figure 5A).
Qualitative examination of the host anatomical response to the presence of hNPCctx or hNPCctx - GDNF revealed substantial preservation of the
photoreceptor outer nuclear
layer (ONL) overlying all subretinal donor cells (Figure 5E and F), with
photoreceptor rescue gradually declining outside the distribution of the transplanted cells (Figure 5E and G).
These cells protect and nourish the retina, remove waste products, prevent new blood vessel growth into the retinal
layer, and absorb light not absorbed by the
photoreceptor cells; these actions prevent the scattering of the light and enhance clarity of vision.
iPS - RPE cells were injected into the subretinal space between the host RPE and
photoreceptor cells (B) A
layer of iPS - RPE cells in the subretinal space of the dystrophic RCS rat 20 hours following transplantation.
Conservation of visual acuity in the iPS - RPE transplanted eyes was associated with the preservation of
photoreceptors in the host outer nuclear
layer (ONL — Fig. 7A), identified by the expression of rhodopsin in the outer segments of
photoreceptors (Fig. 7A inset, Dystrophic + transplant).
The progression of retinal dystrophy in the RCS rat is such that by 13 weeks post-graft most of the ONL has disappeared [33] and the
photoreceptor outer segment
layer is reduced to a debris zone [40], a finding we observed in dystrophic controls.
Inset shows higher resolution confocal images of
photoreceptor cell nuclear
layers (DAPI blue) and rhodopsin expression (red) in the dystrophic control (left inset) and dystrophic with iPS - RPE transplant (right inset) RCS rat.
«This is a reflective
layer so light that is not absorbed by
photoreceptors gets bounced back and forth in the back of the eye to give it another chance at being recognized,» Ryder says.
Layers of the retina: RPE, retinal pigment epithelium; PR,
photoreceptors; ONL, outer nuclear
layer; OPL, outer plexiform
layer; INL, inner nuclear
layer; IPL, inner plexiform
layer; GCL, ganglion cell
layer; NFL, nerve fiber
layer.