Photoreceptor cell

This article is about cellular photoreceptors. For other types of photoreceptors, see Photoreceptor (disambiguation).

"Rods and cones" redirects here. For the Blue Man Group song, see Rods and Cones (song).

Neuron: Photoreceptor Cell
Functional parts of the rods and cones, which are two of the three types of photosensitive cells in the retina
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A photoreceptor cell is a specialized type of neuron found in the eye's retina that is capable of phototransduction. The great biological importance of photoreceptors is that they convert light (electromagnetic radiation) into signals that can stimulate biological processes. To be more specific, photoreceptor proteins in the cell absorb photons, triggering a change in the cell's membrane potential.

The two classic photoreceptor cells are rods and cones, each contributing information used by the visual system to form a representation of the visual world, sight. The rods are narrower than the cones and distributed differently across the retina, but the chemical process in each that supports phototransduction is similar.^[1] A third class of photoreceptor cells was discovered during the 1990s:^[2] the photosensitive ganglion cells. These cells do not contribute to sight directly, but are thought to support circadian rhythms and pupillary reflex.

There are major functional differences between the rods and cones. Rods are extremely sensitive, and can be triggered by a very small number of photons.^[3] At very low light levels, visual experience is calculated solely from the rod signal. This explains why colors cannot be seen at low light levels: Only one type of photoreceptor cell is active.

Cones require significantly brighter light (i.e., a larger numbers of photons) in order to produce a signal. In humans, there are three different types of cone cell, distinguished by their pattern of response to different wavelengths of light. Color experience is calculated from these three distinct signals, perhaps via an opponent process.^[4] The three types of cone cell respond (roughly) to light of short, medium, and long wavelengths. Note that, due to the principle of univariance, the firing of the cell depends upon only the number of photons absorbed. The different responses of the three types of cone cells are determined by the likelihoods that their respective photoreceptor proteins will absorb photons of different wavelengths. So, for example, an L cone cell contains a photoreceptor protein that more readily absorbs long wavelengths of light (i.e., more "red"). Light of a shorter wavelength can also produce the same response, but it must be much brighter to do so.

The human retina contains about 120 million rod cells and 5 million cone cells. The number and ratio of rods to cones varies among species, dependent on whether an animal is primarily diurnal or nocturnal. Certain owls have a tremendous number of rods in their retinas — the eyes of the tawny owl are approximately 100 times more sensitive at night than those of humans.^[5] There are about 1.3 million ganglion cells in the human visual system; 1 to 2% of them are photosensitive.

Described here are vertebrate photoreceptors. Invertebrate photoreceptors in organisms such as insects and molluscs are different in both their morphological organization and their underlying biochemical pathways.

Histology

Anatomy of a Rod Cell^[6]

Rod and cone photoreceptors are found on the outermost layer of the retina; they both have the same basic structure. Closest to the visual field (and farthest from the brain) is the axon terminal, which releases a neurotransmitter called glutamate to bipolar cells. Farther back is the cell body, which contains the cell's organelles. Farther back still is the inner segment, a specialized part of the cell full of mitochondria. The chief function of the inner segment is to provide ATP (energy) for the sodium-potassium pump. Finally, closest to the brain (and farthest from the field of view) is the outer segment, the part of the photoreceptor that absorbs light. Outer segments are actually modified cilia that contain disks filled with opsin, the molecule that absorbs photons, as well as voltage-gated sodium channels.

The membranous photoreceptor protein opsin contains a pigment molecule called retinal. In rod cells, these together are called rhodopsin. In cone cells, there are different types of opsins that combine with retinal to form pigments called photopsins. Three different classes of photopsins in the cones react to different ranges of light frequency, a differentiation that allows the visual system to calculate color. The function of the photoreceptor cell is to convert the light energy of the photon into a form of energy communicable to the nervous system and readily usable to the organism: This conversion is called signal transduction.

The opsin found in the photosensitive ganglion cells of the retina that are involved in various reflexive responses of the brain and body to the presence of (day)light, such as the regulation of circadian rhythms, pupillary reflex and other non-visual responses to light, is called melanopsin. Atypical in vertebrates, melanopsin functionally resembles invertebrate opsins. In structure, it is an opsin, a retinylidene protein variety of G-protein-coupled receptor.

When light activates the melanopsin signaling system, the melanopsin-containing ganglion cells discharge nerve impulses that are conducted through their axons to specific brain targets. These targets include the olivary pretectal nucleus (a center responsible for controlling the pupil of the eye), the LGN, and, through the retinohypothalamic tract (RHT), the suprachiasmatic nucleus of the hypothalamus (the master pacemaker of circadian rhythms). Melanopsin-containing ganglion cells are thought to influence these targets by releasing from their axon terminals the neurotransmitters glutamate and pituitary adenylate cyclase activating polypeptide (PACAP).

Humans

Normalized human photoreceptor absorbances for different wavelengths of light^[7]

The human retina has approximately 5 million cones and 120 million rods. Signals from the rods and cones converge on ganglion and bipolar cells for preprocessing before they are sent to the lateral geniculate nucleus. At the "center" of the retina (the point directly behind the lens) is the fovea, which contains only cone photoreceptor cells; this is the region capable of producing the highest visual acuity. Across the rest of the retina, rods and cones are intermingled. No photoreceptors are found at the blind spot, the area where ganglion cell fibers are collected into the optic nerve and leave the eye.^[8]

The photoreceptor proteins in the three types of cones differ in their sensitivity to photons of different wavelengths (see graph). Since cones respond to both the wavelength and intensity of light, the cone's sensitivity to wavelength is measured in terms of its relative rate of response if the intensity of a stimulus is held fixed, while the wavelength is varied. From this, in turn, is inferred the absorbance.^[9] The graph normalizes the degree of absorbance on a hundred point scale. For example, the S cone's relative response peaks around 420 nm (nanometers, a measure of wavelength). This tells us that an S cone is more likely to absorb a photon at 420 nm than at any other wavelength. If light of a different wavelength to which it is less sensitive, say 480 nm, is increased in brightness appropriately, however, it will produce exactly the same response in the S cone. So, the colors of the curves are misleading. Cones cannot detect color by themselves; rather, color vision requires comparison of the signal across different cone types.

Phototransduction

Phototransduction is the complex process whereby the energy of a photon is used to change the inherent membrane potential of the photoreceptor. This change thereby signals to the nervous system that light is in the visual field.

Activation of rods and cones is actually hyperpolarization; when they are not being stimulated, they depolarize and release glutamate continuously. In the dark, cells have a relatively high concentration of cyclic guanosine 3'-5' monophosphate (cGMP), which opens ion channels (largely sodium channels, though calcium can enter through these channels as well). The positive charges of the ions that enter the cell down its electrochemical gradient change the cell's membrane potential, cause depolarization, and lead to the release of the neurotransmitter glutamate. Glutamate can depolarize some neurons and hyperpolarize others.

When light hits a photoreceptive pigment within the photoreceptor cell, the pigment changes shape. The pigment, called iodopsin or rhodopsin, consists of large proteins called opsin (situated in the plasma membrane), attached to a covalently bound prosthetic group: an organic molecule called retinal (a derivative of vitamin A). The retinal exists in the 11-cis-retinal form when in the dark, and stimulation by light causes its structure to change to all-trans-retinal. This structural change causes it to activate a regulatory protein called transducin, which leads to the activation of cGMP phosphodiesterase, which breaks cGMP down into 5'-GMP. Reduction in cGMP allows the ion channels to close, preventing the influx of positive ions, hyperpolarizing the cell, and stopping the release of neurotransmitters.^[10] The entire process by which light initiates a sensory response is called visual phototransduction.

Dark current

Unstimulated (in the dark), cyclic-nucleotide gated channels in the outer segment are open because cyclic GMP (cGMP) is bound to them. Hence, positively charged ions (namely sodium ions) enter the photoreceptor, depolarizing it to about −40 mV (resting potential in other nerve cells is usually −65 mV). This depolarizing current is often known as dark current.

Signal transduction pathway

The signal transduction pathway is the mechanism by which the energy of a photon signals a mechanism in the cell that leads to its electrical polarization. This polarization ultimately leads to either the transmittance or inhibition of a neural signal that will be fed to the brain via the optic nerve. The steps, or signal transduction pathway, in the vertebrate eye's rod and cone photoreceptors are then:

1. The rhodopsin or iodopsin in the outer segment absorbs a photon, changing the configuration of a retinal Schiff base cofactor inside the protein from the cis-form to the trans-form, causing the retinal to change shape.
2. This results in a series of unstable intermediates, the last of which binds stronger to the G protein in the membrane and activates transducin, a protein inside the cell. This is the first amplification step – each photoactivated rhodopsin triggers activation of about 100 transducins. (The shape change in the opsin activates a G protein called transducin.)
3. Each transducin then activates the enzyme cGMP-specific phosphodiesterase (PDE).
4. PDE then catalyzes the hydrolysis of cGMP. This is the second amplification step, where a single PDE hydrolyses about 1000 cGMP molecules. (The enzyme hydrolyzes the second messenger cGMP to GMP)
5. With the intracellular concentration of cGMP reduced, the net result is closing of cyclic nucleotide-gated ion channels in the photoreceptor membrane because cGMP was keeping the channels open. (Because cGMP acts to keep Na⁺ ion channels open, the conversion of cGMP to GMP closes the channels.)
6. As a result, sodium ions can no longer enter the cell, and the photoreceptor hyperpolarizes (its charge inside the membrane becomes more negative). (The closing of Na⁺ channels hyperpolarizes the cell.)
7. This change in the cell's membrane potential causes voltage-gated calcium channels to close. This leads to a decrease in the influx of calcium ions into the cell and thus the intracellular calcium ion concentration falls.
8. The lack of calcium means that less glutamate is released to the bipolar cell than before (see below). (The decreased calcium level slows the release of the neurotransmitter glutamate, which can either excite or inhibit the postsynaptic bipolar cells.)
9. Reduction in the release of glutamate means one population of bipolar cells will be depolarized and a separate population of bipolar cells will be hyperpolarized, depending on the nature of receptors (ionotropic or metabotropic) in the postsynaptic terminal (see receptive field).

Thus, a rod or cone photoreceptor actually releases less neurotransmitter when stimulated by light.

ATP provided by the inner segment powers the sodium-potassium pump. This pump is necessary to reset the initial state of the outer segment by taking the sodium ions that are entering the cell and pumping them back out.

Although photoreceptors are neurons, they do not conduct action potentials with the exception of the photosensitive ganglion cell - which are involved mainly in the regulation of circadian rhythms, melatonin, and pupil dilation.

Advantages

Phototransduction in rods and cones is unique in that the stimulus (in this case, light) actually reduces the cell's response or firing rate, which is unusual for a sensory system where the stimulus usually increases the cell's response or firing rate. However, this system offers several key advantages.

First, the classic (rod or cone) photoreceptor is depolarized in the dark, which means many sodium ions are flowing into the cell. Thus, the random opening or closing of sodium channels will not affect the membrane potential of the cell; only the closing of a large number of channels, through absorption of a photon, will affect it and signal that light is in the visual field. Hence, the system is noiseless.

Second, there is a lot of amplification in two stages of classic phototransduction: one pigment will activate many molecules of transducin, and one PDE will cleave many cGMPs. This amplification means that even the absorption of one photon will affect membrane potential and signal to the brain that light is in the visual field. This is the main feature that differentiates rod photoreceptors from cone photoreceptors. Rods are extremely sensitive and have the capacity of registering a single photon of light, unlike cones. On the other hand, cones are known to have very fast kinetics in terms of rate of amplification of phototransduction, unlike rods.

Difference between rods and cones

Comparison of human rod and cone cells, from Eric Kandel et al. in Principles of Neural Science.^[10]

Rods	Cones
Used for scotopic vision (vision under low light conditions)	Used for photopic vision (vision under high light conditions)
Very light sensitive; sensitive to scattered light	Not very light sensitive; sensitive to only direct light
Loss causes night blindness	Loss causes legal blindness
Low visual acuity	High visual acuity; better spatial resolution
Not present in fovea	Concentrated in fovea
Slow response to light, stimuli added over time	Fast response to light, can perceive more rapid changes in stimuli
Have more pigment than cones, so can detect lower light levels	Have less pigment than rods, require more light to detect images
Stacks of membrane-enclosed disks are unattached to cell membrane directly	Disks are attached to outer membrane
20 times more rods than cones in the retina
One type of photosensitive pigment	Three types of photosensitive pigment in humans
Confer achromatic vision	Confer color vision

Function

Photoreceptors do not signal color; they only signal the presence of light in the visual field.

A given photoreceptor responds to both the wavelength and intensity of a light source. For example, red light at a certain intensity can produce the same exact response in a photoreceptor as green light of a different intensity. Therefore, the response of a single photoreceptor is ambiguous when it comes to color.

To determine color, the visual system compares responses across a population of photoreceptors (specifically, the three different cones with differing absorption spectra). To determine intensity, the visual system computes how many photoreceptors are responding. This is the mechanism that allows trichromatic color vision in humans and some other animals.

Signaling

The rod and cone photoreceptors signal their absorption of photons via a decrease in the release of the neurotransmitter glutamate to bipolar cells at its axon terminal. Since the photoreceptor is depolarized in the dark, a high amount of glutamate is being released to bipolar cells in the dark. Absorption of a photon will hyperpolarize the photoreceptor and therefore result in the release of less glutamate at the presynaptic terminal to the bipolar cell.

Every rod or cone photoreceptor releases the same neurotransmitter, glutamate. However, the effect of glutamate differs in the bipolar cells, depending upon the type of receptor imbedded in that cell's membrane. When glutamate binds to an ionotropic receptor, the bipolar cell will depolarize (and therefore will hyperpolarize with light as less glutamate is released). On the other hand, binding of glutamate to a metabotropic receptor results in a hyperpolarization, so this bipolar cell will depolarize to light as less glutamate is released.

In essence, this property allows for one population of bipolar cells that gets excited by light and another population that gets inhibited by it, even though all photoreceptors show the same response to light. This complexity becomes both important and necessary for detecting color, contrast, edges, etc.

Further complexity arises from the various interconnections among bipolar cells, horizontal cells, and amacrine cells in the retina. The final result is differing populations of ganglion cells in the retina, a sub-population of which is also intrinsically photosensitive, using the photopigment melanopsin.

Ganglion cell (non-rod non-cone) photoreceptors

A non-rod non-cone photoreceptor in the eyes of mice, which was shown to mediate circadian rhythms, was discovered in 1991 by Foster et al.^[2] These neuronal cells, called intrinsically photosensitive retinal ganglion cells (ipRGC), are a small subset (~1–3%) of the retinal ganglion cells located in the inner retina, that is, in front^[11] of the rods and cones located in the outer retina. These light sensitive neurons contain a photopigment, melanopsin,^{[12][13][14][15][16]} which has an absorption peak of the light at a different wavelength (~480 nm^[17]) than rods and cones. Beside circadian / behavioral functions, ipRGCs have a role in initiating the pupillary light reflex.^[18]

Dennis Dacey with colleagues showed in a species of Old World monkey that giant ganglion cells expressing melanopsin projected to the lateral geniculate nucleus (LGN).^[19] Previously only projections to the midbrain (pre-tectal nucleus) and hypothalamus (suprachiasmatic nucleus) had been shown. However a visual role for the receptor was still unsuspected and unproven.

In 2007, Farhan H. Zaidi and colleagues published pioneering work using rodless coneless humans. Current Biology subsequently announced in their 2008 editorial, commentary and despatches to scientists and ophthalmologists, that the non-rod non-cone photoreceptor had been conclusively discovered in humans using landmark experiments on rodless coneless humans by Zaidi and colleagues^{[16][20][21][22]} As had been found in other mammals, the identity of the non-rod non-cone photoreceptor in humans was found to be a ganglion cell in the inner retina. The workers had tracked down patients with rare diseases wiping out classic rod and cone photoreceptor function but preserving ganglion cell function.^[20][21][22] Despite having no rods or cones the patients continued to exhibit circadian photoentrainment, circadian behavioural patterns, melanopsin suppression, and pupil reactions, with peak spectral sensitivities to environmental and experimental light matching that for the melanopsin photopigment. Their brains could also associate vision with light of this frequency.

In humans the retinal ganglion cell photoreceptor contributes to conscious sight as well as to non-image-forming functions like circadian rhythms, behaviour and pupil reactions.^[23] Since these cells respond mostly to blue light, it has been suggested that they have a role in mesopic vision^{[citation needed]}. Zaidi and colleagues' work with rodless coneless human subjects hence also opened the door into image-forming (visual) roles for the ganglion cell photoreceptor. It was discovered that there are parallel pathways for vision – one classic rod and cone-based pathway arising from the outer retina, and the other a rudimentary visual brightness detector pathway arising from the inner retina, which seems to be activated by light before the other.^[23] Classic photoreceptors also feed into the novel photoreceptor system, and colour constancy may be an important role as suggested by Foster. The receptor could be instrumental in understanding many diseases including major causes of blindness worldwide like glaucoma, a disease that affects ganglion cells, and the study of the receptor offered potential as a new avenue to explore in trying to find treatments for blindness. It is in these discoveries of the novel photoreceptor in humans and in the receptors role in vision, rather than its non-image-forming functions, where the receptor may have the greatest impact on society as a whole, though the impact of disturbed circadian rhythms is another area of relevance to clinical medicine.

Most work suggests that the peak spectral sensitivity of the receptor is between 460 and 482 nm. Steven Lockley et al. in 2003 showed that 460 nm wavelengths of light suppress melatonin twice as much as longer 555 nm light. However, in more recent work by Farhan Zaidi et al., using rodless coneless humans, it was found that what consciously led to light perception was a very intense 481 nm stimulus; this means that the receptor, in visual terms, enables some rudimentary vision maximally for blue light.^[23]

Sports

See also: Eye black

As rods are much slower to respond to light stimulation than cones, viewing sporting events such as baseball becomes gradually harder as daylight subsides.^[24]

See also

• Visual phototransduction
• G protein-coupled receptor
• Sensory system
• Photosensitive
• Photosensitive ganglion cell
• Horizontal cell
• Bipolar cell
• Amacrine cell

References

1. ^ "eye, human." Encyclopædia Britannica. Encyclopaedia Britannica Ultimate Reference Suite. Chicago: Encyclopædia Britannica, 2010.
2. ^ ^{a b} Foster, R.G.; Provencio, I.; Hudson, D.; Fiske, S.; Grip, W.; Menaker, M. (1991). "Circadian photoreception in the retinally degenerate mouse (rd/rd)". Journal of Comparative Physiology A 169 (1). doi:10.1007/BF00198171. 
3. ^ Hecht, S.; Shlar, S.; Pirenne, M.H. (1942). "Energy, Quanta, and Vision". Journal of General Physiology 25: 819–840. doi:10.1085/jgp.25.6.819. PMC 2142545. PMID 19873316. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2142545. 
4. ^ Hurvich, Leo (1981). Color Vision. Sinauer. 
5. ^ "Owl Eyesight" at owls.org
6. ^ Human Physiology and Mechanisms of Disease by Arthur C. Guyton (1992) ISBN 0721632998 p. 373
7. ^ Bowmaker J.K. and Dartnall H.J.A. (1980). "Visual pigments of rods and cones in a human retina". J. Physiol. 298: 501–511. PMC 1279132. PMID 7359434. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1279132. 
8. ^ Goldstein, E. Bruce (2007). Sensation and Perception (7 ed.). Thomson and Wadswoth. 
9. ^ Wandell, Brian A. (1995). Foundations of Vision. Sinauer. 
10. ^ ^{a b} Kandel, E. R.; Schwartz, J.H.; Jessell, T.M. (2000). Principles of Neural Science (4th ed.). New York: McGraw-Hill. pp. 507–513. ISBN 0-8385-7701-6. 
11. ^ See retina for information on the retinal layer structure.
12. ^ Provencio, I. et al. (2000-01-15). "A human opsin in the inner retina". The Journal of Neuroscience 20 (2): 600–605. PMID 10632589. 
13. ^ Hattar, S.; Liao, HW; Takao, M; Berson, DM; Yau, KW (2002). "Melanopsin-Containing Retinal Ganglion Cells: Architecture, Projections, and Intrinsic Photosensitivity". Science 295 (5557): 1065–70. Bibcode 2002Sci...295.1065H. doi:10.1126/science.1069609. PMC 2885915. PMID 11834834. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2885915. 
14. ^ Melyan, Z.; Tarttelin, E. E.; Bellingham, J.; Lucas, R. J.; Hankins, M. W. (2005). "Addition of human melanopsin renders mammalian cells photoresponsive". Nature 433 (7027): 741–5. Bibcode 2005Natur.433..741M. doi:10.1038/nature03344. PMID 15674244. 
15. ^ Qiu, Xudong; Kumbalasiri, Tida; Carlson, Stephanie M.; Wong, Kwoon Y.; Krishna, Vanitha; Provencio, Ignacio; Berson, David M. (2005). "Induction of photosensitivity by heterologous expression of melanopsin". Nature 433 (7027): 745–9. Bibcode 2005Natur.433..745Q. doi:10.1038/nature03345. PMID 15674243. 
16. ^ ^{a b} Vangelder, R (2008). "Non-Visual Photoreception: Sensing Light without Sight". Current Biology 18 (1): R38. doi:10.1016/j.cub.2007.11.027. PMID 18177714. 
17. ^ Berson, David M. (2007). "Phototransduction in ganglion-cell photoreceptors". Pflügers Archiv - European Journal of Physiology 454 (5): 849–55. doi:10.1007/s00424-007-0242-2. PMID 17351786. 
18. ^ Lucas, Robert J.; Douglas, Ronald H.; Foster, Russell G. (2001). "Characterization of an ocular photopigment capable of driving pupillary constriction in mice.". Nature Neuroscience 4 (6): 621–6. doi:10.1038/88443. PMID 11369943. 
19. ^ Dacey, Dennis M.; Liao, Hsi-Wen; Peterson, Beth B.; Robinson, Farrel R.; Smith, Vivianne C.; Pokorny, Joel; Yau, King-Wai; Gamlin, Paul D. (2005). "Melanopsin-expressing ganglion cells in primate retina signal colour and irradiance and project to the LGN". Nature 433 (7027): 749–54. Bibcode 2005Natur.433..749D. doi:10.1038/nature03387. PMID 15716953. 
20. ^ ^{a b} Genova, Cathleen, Blind humans lacking rods and cones retain normal responses to nonvisual effects of light. Cell Press, December 13, 2007.
21. ^ ^{a b} Coghlan A. Blind people 'see' sunrise and sunset. New Scientist, 26 December 2007, issue 2635.
22. ^ ^{a b} Medical News Today. Normal Responses To Non-visual Effects Of Light Retained By Blind Humans Lacking Rods And Cones. 14 December 2007.
23. ^ ^{a b c} Zaidi FH et al. (2007). "Short-wavelength light sensitivity of circadian, pupillary, and visual awareness in humans lacking an outer retina.". Current biology : CB 17 (24): 2122–8. doi:10.1016/j.cub.2007.11.034. PMC 2151130. PMID 18082405. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2151130. 
24. ^ "Webvision: Photoreceptors". Webvision.med.utah.edu. http://webvision.med.utah.edu/photo2.html. Retrieved 2010-12-12. 

Bibliography

• Campbell, Neil A., and Reece, Jane B. (2002). Biology. San Francisco: Benjamin Cummings. pp. 1064–1067. ISBN 0-8053-6624-5. 
• Freeman, Scott (2002). Biological Science (2nd Edition). Englewood Cliffs, N.J: Prentice Hall. pp. 835–837. ISBN 0-13-140941-7. 

External links

• NIF Search – Photoreceptor Cell via the Neuroscience Information Framework