The receptor also regulates DHA retention and conservation in cells in the eye and is necessary for
photoreceptor cell function.
Not exact matches
He suspects that transplanted
cells are actually restoring the
function of «dormant»
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 six previously known fly rhodopsins account for the full
function of
photoreceptor cells in the fly's eyes, so although the fruit fly genome contained the sequence of a seventh rhodopsin, the role of Rh7 was unclear.
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.
With age, our eyes accumulate waste in retinal pigment epithelium (RPE), which supports the life and
function of
photoreceptors (light sensitive
cells in the eye); in advanced stages, RPE and
photoreceptors die.
One can imagine that loss of
function of any of the gene products along this complex pathway could lead to severe consequences for the survival of the
photoreceptor (PR)
cells in the eye.
Of note, while vision rescue requires preservation of some functional
photoreceptors, the mere presence of
photoreceptor cells in the ONL of transplanted RCS rats does not assure
function [61].
It is likely that those
cells would then support the
function of the very important
photoreceptor cells in the retina.
The retinal pigment epithelium (RPE) is a monolayer of
cells, residing at the back of the eye between Bruch's membrane and the retina, which is essential for
photoreceptor function and survival.
As a monolayer of
cells critical to
photoreceptor function and survival, the RPE is an ideally accessible target for cellular therapy.
Although known to have neuronal
cell functions STK38L has not previously been associated with abnormal
photoreceptor function; being associated with such a disease in dogs establishes this gene as a potential candidate for similar diseases in other species, including man.
The gene product's precise role is not currently understood but it is thought to anchor regulatory complexes at the
photoreceptor connecting cilium, which acts as a bridge between the inner and outer segments of
photoreceptor cells [43] as well as having
functions in disk morphogenesis [42] and in the structure of the ciliary axoneme [44].
ERG abnormalities are evident by 5 — 6 weeks of age and
cell degeneration is present by 4 months, suggesting the mutant protein has a toxic gain of
function that severely compromises the early stage of development of the
photoreceptors.
Whereas the genes implicated in early - onset diseases are those necessary for the correct development of
photoreceptors the genes associated with later - onset forms of disease are those necessary for the long - term maintenance and
function of these
cells.