Research Paper: Intrinsically Photosensitive Retinal Ganglion Cell

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[. . .] The ganglion cells are what constitute the intrinsic photosensitive response in the visualizing system. In the retina, the normal photoreceptive cells are of two types, the rod and cone [6]. The functioning of the rod is similar to that of specialized neurons converting the visual stimuli in the form of photons into chemical and electrical stimuli that the central nervous system can process. The rod responds to a wide range of light intensities. They are responsible for the cases of visualizing the size, shape and brightness f image. The cone cells, on the contrary, have the same stature as the rods. However, they have a difference in perceiving the light as photoreceptors. They are responsible for establishing the aspects of color and fine details. The rods are many in number that the cones and largely sensitive to a wide range of light intensities. The rods have the rhodopsin, which consists of the protein called opsin among with a photosensitive chemical from vitamin A

In comparison of the photoreceptors, the cone and rods verses the intrinsic photosensitive retinal ganglion there are notable differences that emerge. The differences are unique, with the most notable differences being the following. Firstly, there is depolarizing of the light response in the intrinsically photosensitive retinal ganglion cells [11]. This is contrary to the hyperpolarizing response exhibited by the rods and cones. The polarizing effect contributes to the difference in the ability to focalize light. The cones and rods, due to the hyperpolarizing effect can visualize a wide variety of light intensities as compared to depolarizing which limits the light detection intensities. Secondly, in comparison, the intrinsically photosensitive retinal ganglion cells have less sensitivity to light that the classical photoreceptor cells. Additionally, they perceive signal with much slow kinetics. This high sensitivity is what sets the intrinsic sensitivity unique. In view of the normal wave detections by the classical photoreceptor cells, the difference in the wide variety of wavelengths that the rod and cone cells detect is covered in this property of the ipRGCs. The intrinsically photosensitive retinal ganglion cells can detect waves with remarkably low kinetics [4]. The ability to detect these slow kinetics waves is due to the technical involvement of the light sensitivity process. Therefore, despite them having limited wavelength range, they can detect waves that no other retinal cells can detect.

Another difference between these photoreceptors is the ability to maintain a sustained light response under conditions of continuous bright illumination. The ipRGCs have the ability to withstand the long exposure to continuous bright illumination. They can withstand this exposure and continue to encode the stimuli energy faithfully over a long period. This is unlike the cones and rods that break after long exposure to bright illumination. The cones and rods, after the long exposure, react in a manner that causes hurt to the eyes. However, the ipRGCs sustain the severe weather challenges, maintaining the contact between the illumination and observer as necessary [1]. The other retinal cells cannot represent the peace and ambience in the levels of light. In this version, the characteristic of the dendrites responding to stimuli rather than the normal cell of the eye is worth. The dendrites of the intrinsically photosensitive retinal ganglion cells have an inbuilt ability to initiate the procedure of detecting the signal. The dendrites of the ganglion cells have an overlapping layer of dendrite fields, making what the scholars' established the photoreceptive net. Therefore, these features facilitate the intrinsically photosensitive ganglion cells working towards meeting the role of the diffuse stimuli. The feature also facilitates the vision in the people as they absorb the ambient light waves and establish the behavior of cells. For instance, the cells with densely populated dendrites forming larger net structures couple well in contributing to other factors of visualizing from via the photo entrainment a wave-length pupillary reflex. Thus, the ipRGCs come in hand in establishing the images and thoughts of meeting certain reflex actions of the eyes [3]. Moreover, there are other procedures distinguish the cells. The intrinsically photosensitive retinal ganglion cells have a vast action of spectrum. The wide spectrum of the ganglion cells has an expansive venue of cell reporting, providing the cells with a resolution spectrum for image development and analysis. The cone and rods have a wavelength limitation compared to the ganglion cells. The cells of the ipRGCs sent signals directly to the essential nervous system for scrutiny. The reason the differences vary this extensively is that the ipRGCs utilize melanopsin as the leading abstract.

Its functional role in light detection, and the purpose of the ipRGC

The detection process of light via the intrinsically sensitive lights includes a dramatic difference from that of the rods and cones. Notably, there is an aspect of a depolarizing light response within these ipRGCs [2]. This is different from the hyperpolarizing effect the rods and cones depict in their functioning. Additionally, there is the expression of less sensitivity to light than the usual photoreceptors. These differences in the wave detection procedures of the photoreceptor verses that of the rods and cones are what constitutes the difference; in these two procedures of detecting and signaling light for the central nervous system.

The pigment of the ipRGCs includes the ciliary cells that aid in the detection of light and movement. The intrinsic movements within the mammalian eye are responsible for various activities in the body system. The ipRGCs are responsible for the rhythmic movements of the eye; hence, the physiology and behavior of the collective circadian rhythms. The movement in these cells entails a tiny cluster of called within the suprachiasmatic muscle (SCN) [11]. The near 24-hour eye elements lead to ultimate change in the behaviors. The animals rely on the environment to determine darkness and light phases; thus, the SCN must entrain when they are young to know they should work. The light ipRGCs is the primary carrier of daily signals. Therefore, these photoreceptors do facilitate the power that the intrinsically photosensitive retinal ganglion cells weld in science.

The molecular mechanisms of photo transduction in the ipRGC

The molecular functioning of the ganglion cells translates the signals of light perceived by the eye system into signals that the central nervous system can withstand. The photo transduction process of the eye is where the pigments record the information. The section is the cells ciliary, the outer segment of the eye retina. There are various components involved in the procedure of transduction. Firstly, the components that constitute the process have limits. In transducing the interactions within the retina cells, the following mechanisms ensue. The essential part is the photoisomerizing of the active Rh [7]. The active Rh then activates the G-protein transducin which then leads to the stimulation of a phosphodieterase (PDE) that hydrolyzes specific cGMP. The G-protein transducin and the PDE have peripheral locations consisting of membrane proteins. The procedure that ensues in the event of darkness is as follows. In darkness, the cGMP has a higher concentration within the system. Therefore, by the process of direct binding, it maintains the cGMP gated in a nonselective cat ion channels within the plasma membrane in an open state. The channels that open have an unusual property that shows desensitization to ligand [5]. This assists in maintain a steady inward current in time of darkness. This then depolarizes the cell sufficiently, at potential of -30mV to sustain the synaptic transmitter release of glutamate. The light that this system induces undergoes grading to decrease into free cGMP and thus the cGMP gated channels close. Thus, hyperpolarizing the cells and reducing or stopping the glutamate release does not fire action potentials. The Rh activates the G. protein through random diffusion encounters between the disc membranes. The procedure continues until the initial Rh multiplies the world up to ten power three, during a single photon response, which lasts up to one second at the normal room temperature. However, during a mouse single rod photon response, only up to 20 glutamate transducin [9]. Nonetheless, this remains a substantial amplification in the signaling process. Additionally, the high hydrolytic rate of the PDE that are active provides an additional amplification for the signal. The high power transduction is of way higher transduction than the normal rod photo transduction. Therefore, skill of understanding the procedure of transformation will not last; and the rhodopsin exists as a monomer and takes one only one absorbed photon to trigger Photo transduction. The melanopsin does not require heavy procedure to deactivate.

For the wholesome deactivation of the photo, transduction is remarkably a complex process. For the complete deactivation of the photo transduction, all the Rh must shut down. The procedure then leads to a decay over a minute into an inactive state from meta II to meta III, before the decay is complete there is phophorylation of the Rh by rhodopsin kinase (also called G. protein coupled receptor kinase)[5] . After this process, rapid binding of the protein arrestin which identifies the phosphorylated Rh loses all… [END OF PREVIEW]

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APA Format

Intrinsically Photosensitive Retinal Ganglion Cell.  (2013, October 14).  Retrieved March 23, 2019, from

MLA Format

"Intrinsically Photosensitive Retinal Ganglion Cell."  14 October 2013.  Web.  23 March 2019. <>.

Chicago Format

"Intrinsically Photosensitive Retinal Ganglion Cell."  October 14, 2013.  Accessed March 23, 2019.