Cited by 335Retinal Development and DisordersPhotoreceptor and optogenetics researchRetinal Diseases and Treatments

The Cone-specific visual cycle

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Wang, Jin-Shan, Kefalov, Vladimir J.·2011·Progress in Retinal and Eye Research

Abstract

Cone photoreceptors mediate our daytime vision and function under bright and rapidly-changing light conditions. As their visual pigment is destroyed in the process of photoactivation, the continuous function of cones imposes the need for rapid recycling of their chromophore and regeneration of their pigment. The canonical retinoid visual cycle through the retinal pigment epithelium cells recycles chromophore and supplies it to both rods and cones. However, shortcomings of this pathway, including its slow rate and competition with rods for chromophore, have led to the suggestion that cones might use a separate mechanism for recycling of chromophore. In the past four decades biochemical studies have identified enzymatic activities consistent with recycling chromophore in the retinas of cone-dominant animals, such as chicken and ground squirrel. These studies have led to the hypothesis of a cone-specific retina visual cycle. The physiological relevance of these studies was controversial for a long time and evidence for the function of this visual cycle emerged only in very recent studies and will be the focus of this review. The retina visual cycle supplies chromophore and promotes pigment regeneration only in cones but not in rods. This pathway is independent of the pigment epithelium and instead involves the Müller cells in the retina, where chromophore is recycled and supplied selectively to cones. The rapid supply of chromophore through the retina visual cycle is critical for extending the dynamic range of cones to bright light and for their rapid dark adaptation following exposure to light. The importance of the retina visual cycle is emphasized also by its preservation through evolution as its function has now been demonstrated in species ranging from salamander to zebrafish, mouse, primate, and human.

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Crossref · 10.1016/j.preteyeres.2010.11.001

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  • The visual pigments in rods and cones are rhodopsin and iodopsin, respectively.

    “The visual pigments in rods and cones are rhodopsin (RHO) and iodopsin, respectively.”

    From The Role of Vitamin A in Retinal Diseases (2022) · cites this paper as [52]

    Section 1.2, “Visual pigment,” identifies rhodopsin as the rod pigment but calls the cone counterpart “cone pigment,” not iodopsin. Iodopsin appears in the References as a paper title, but our copy does not identify it as the visual pigment in cones. (LLM, conf=0.88)

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  • Several lines of evidence suggest that cone photoreceptors may have access to a special source of visual chromophore that rods do not have.

    “several lines of evidence indicate that cone photoreceptors might have access to a special source of visual chromophore not available to rods85”

    From Chemistry of the Retinoid (Visual) Cycle (2014) · cites this paper as [85]

  • Inner retinal ARAT activity is associated with chicken Müller cells in primary culture.

    “Studies involving primary cultures of chicken Müller cells indicate that inner retinal ARAT enzymatic activity is associated with this cell type.85,302,431”

    From Chemistry of the Retinoid (Visual) Cycle (2014) · cites this paper as [85]

  • Evidence indicates a second retinoid cycle in the vertebrate retina operates alongside the classic cycle to enable fast cone pigment regeneration.

    “Recent evidence suggests the existence of a second retinoid visual cycle within the vertebrate retina functioning in parallel with the classic visual cycle to specifically support rapid cone pigment regeneration (Figure 5; for reviews, see (Muniz et al., 2007; Wang and Kefalov, 2011; Wolf, 2004)).”

    From New insights into retinoid metabolism and cycling within the retina (2013) · cites this paper as Wang and Kefalov, 2011

  • Because rods depend entirely on 11-cis-retinal and cones can also utilize 11-cis-retinol, competition for this visual cycle product is avoided.

    “As rods depend entirely on 11-cis-retinal and cones can also utilize 11-cis-retinol, the competition for this visual cycle product is avoided [52,63,65,66].”

    From The Role of Vitamin A in Retinal Diseases (2022) · cites this paper as [52]

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References 154 · Cited by 335

Research works printed but not linked: 1

  1. Krebs W Krebs IP Hollyfield JG 1982 Quantitative morphology of the bovine eye The Structure of the Eye New York Elsevier Biomedical 175 182

Authors
Wang, J.-S., & Kefalov, V. J.
Affiliations
Washington University in St. Louis (US)
Venue
Progress in Retinal and Eye Research
Publisher
Elsevier BV
Published
2011-03
Volume
30
Issue
2
Pages
115-128
ISSN
1350-9462 (ISSN-L)
OpenAlex
W1973652650
Cited by
335
References
154
Citations by year
2026: 14 · 2025: 19 · 2024: 20 · 2023: 25 · 2022: 21 · 2021: 31 · 2020: 31 · 2019: 34 · 2018: 26 · 2017: 17 · 2016: 11 · 2015: 28 · 2014: 11 · 2013: 14 · 2012: 15
FWCI
1.32
Type
journal article
Language
en
Open access
Locations
  • Progress in Retinal and Eye Research (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Research to Prevent Blindness
  • NIH (EY019312, EY019543)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinal Development and Disorders
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Photoreceptor and optogenetics research
  • Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
Keywords
cone photoreceptors, Müller cells, rhodopsin regeneration, retinal pigment epithelium, dark adaptation, dynamic range
MeSH terms
Animals, Humans, Light, Models, Biological, Primates, Retina, Retinal Pigments, Caudata, Vision, Ocular, Retinal Rod Photoreceptor Cells, Retinal Cone Photoreceptor Cells, Mice, Retinal Pigment Epithelium

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