Intrinsically photosensitive retinal ganglion cells detect light with a vitamin A-based photopigment, melanopsin

Yingbin Fu, Haining Zhong, Min Hua H Wang, Dong Gen Luo, Hsi Wen Liao, Hidetaka Maeda, Samer Hattar, Laura J. Frishman, King Wai Yau

Research output: Contribution to journalArticle

98 Citations (Scopus)

Abstract

In mammals, intrinsically photosensitive retinal ganglion cells (ipRGCs) mediate non-image-forming visual functions such as pupillary light reflex (PLR) and circadian photoentrainment. This photosensitivity requires melanopsin, an invertebrate opsin-like protein expressed by the ipRGCs. The precise role of melanopsin remains uncertain. One suggestion has been that melanopsin may be a photoisomerase, serving to regenerate an unidentified pigment in ipRGCs. This possibility was echoed by a recent report that melanopsin is expressed also in the mouse retinal pigment epithelium (RPE), a key center for regeneration of rod and cone pigments. To address this question, we studied mice lacking RPE65, a protein essential for the regeneration of rod and cone pigments. Rpe65 -/- ipRGCs were ≃20- to 40-fold less photosensitive than normal at both single-cell and behavioral (PLR) levels but were rescued by exogenous 9-cis-retinal (an 11-cis-retinal analog), indicating the requirement of a vitamin A-based chromophore for ipRGC photosensitivity. In contrast, 9-cis-retinal was unable to restore intrinsic photosensitivity to melanopsin-ablated ipRGCs, arguing against melanopsin functioning merely in photopigment regeneration. Interestingly, exogenous all-trans-retinal was also able to rescue the low sensitivity of rpe65-/- ipRGCs, suggesting that melanopsin could be a bistable pigment. Finally, we detected no melanopsin in the RPE and no changes in rod and cone sensitivities due to melanopsin ablation. Together, these results strongly suggest that melanopsin is the photopigment in the ipRGCs.

Original languageEnglish (US)
Pages (from-to)10339-10344
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume102
Issue number29
DOIs
StatePublished - Jul 19 2005
Externally publishedYes

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Retinal Ganglion Cells
Vitamin A
Light
Vertebrate Photoreceptor Cells
Pupillary Reflex
Regeneration
Retinal Pigment Epithelium
melanopsin
Retinaldehyde
Opsins
Invertebrates
Mammals
Proteins

Keywords

  • Chromophore
  • RPE65

ASJC Scopus subject areas

  • Genetics
  • General

Cite this

Intrinsically photosensitive retinal ganglion cells detect light with a vitamin A-based photopigment, melanopsin. / Fu, Yingbin; Zhong, Haining; Wang, Min Hua H; Luo, Dong Gen; Liao, Hsi Wen; Maeda, Hidetaka; Hattar, Samer; Frishman, Laura J.; Yau, King Wai.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 102, No. 29, 19.07.2005, p. 10339-10344.

Research output: Contribution to journalArticle

Fu, Yingbin ; Zhong, Haining ; Wang, Min Hua H ; Luo, Dong Gen ; Liao, Hsi Wen ; Maeda, Hidetaka ; Hattar, Samer ; Frishman, Laura J. ; Yau, King Wai. / Intrinsically photosensitive retinal ganglion cells detect light with a vitamin A-based photopigment, melanopsin. In: Proceedings of the National Academy of Sciences of the United States of America. 2005 ; Vol. 102, No. 29. pp. 10339-10344.
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abstract = "In mammals, intrinsically photosensitive retinal ganglion cells (ipRGCs) mediate non-image-forming visual functions such as pupillary light reflex (PLR) and circadian photoentrainment. This photosensitivity requires melanopsin, an invertebrate opsin-like protein expressed by the ipRGCs. The precise role of melanopsin remains uncertain. One suggestion has been that melanopsin may be a photoisomerase, serving to regenerate an unidentified pigment in ipRGCs. This possibility was echoed by a recent report that melanopsin is expressed also in the mouse retinal pigment epithelium (RPE), a key center for regeneration of rod and cone pigments. To address this question, we studied mice lacking RPE65, a protein essential for the regeneration of rod and cone pigments. Rpe65 -/- ipRGCs were ≃20- to 40-fold less photosensitive than normal at both single-cell and behavioral (PLR) levels but were rescued by exogenous 9-cis-retinal (an 11-cis-retinal analog), indicating the requirement of a vitamin A-based chromophore for ipRGC photosensitivity. In contrast, 9-cis-retinal was unable to restore intrinsic photosensitivity to melanopsin-ablated ipRGCs, arguing against melanopsin functioning merely in photopigment regeneration. Interestingly, exogenous all-trans-retinal was also able to rescue the low sensitivity of rpe65-/- ipRGCs, suggesting that melanopsin could be a bistable pigment. Finally, we detected no melanopsin in the RPE and no changes in rod and cone sensitivities due to melanopsin ablation. Together, these results strongly suggest that melanopsin is the photopigment in the ipRGCs.",
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