Visual cycle in the mammalian eye. Retinoid-binding proteins and the distribution of 11-cis retinoids

C. D.B. Bridges, R. A. Alvarez, S. L. Fong, F. Gonzalez-Fernandez, D. M.K. Lam, Gregory I Liou

Research output: Contribution to journalArticle

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Abstract

This work was designed to provide an insight into the mammalian visual cycle by investigating the possible function of retinoid-binding proteins in this system, and the distribution and type of 11-cis retinoids present in the interphotoreceptor matrix and the cytosols of the retinal pigment epithelium and retina. The total retinol and retinal in the soluble fractions from these three compartments was 8% (3.31 nmol/eye) of the retinyl palmitate and stearate stored in the pigment epithelium membrane fractions (39 nmol/eye). Only small amounts of retinoids were detected in the rod outer segment cytosol. The insoluble fractions also contained retinol, nearly all of which was found in the retina. The retinoids in the soluble fractions appeared to be bound to cellular retinol-binding protein (CRBP), cellular retinal-binding protein (CRA1BP) and interstitial retinol-binding protein (IRBP, a high-Mr glycoprotein). Using immunospecific precipitation, immunoblot and immunocytochemical techniques it was demonstrated that IRBP was localized in the interphotoreceptor matrix and was synthesized and secreted by the retina, a process that did not require the protein to be glycosylated. The amount of retinol bound to IRBP increased if the eyes were exposed to light, when it was estimated that the protein carried up to 30% of its full capacity for all-trans retinol. In addition to all-trans retinol, IRBP carried smaller amounts of 11-cis retinol. The proportion of 11-cis retinol was frequently higher in eyes that had been protected from illumination, suggesting that IRBP plays a role in rhodopsin regeneration during dark-adaptation. Additionally, endogenous 11-cis retinoids in the retina and RPE cytosols were bound to an Mr 33,000 protein tentatively identified as CRA1BP. The 11-cis retinoid in the retina cytosol was mainly in the form of retinol, while in the RPE cytosol it was mainly in the form of retinal. Substantial amounts of 11-cis retinol were also found in the insoluble (membrane) fraction from the retina. It is suggested that in the mammalian retina 11-cis retinol is generated from all-trans retinol (possibly in the Muller cells). Lack of an 11-cis retinol oxidoreductase in the retina prevents it from being utilized for rhodopsin regeneration until it has been transported to the pigment epithelium, where it is converted to 11-cis retinal and returned to the rod outer segments. It is also suggested that IRBP may be implicated in the transport of retinoids between the rod outer segments, the Muller cells and the pigment epithelium. Proteins that are immunoreactive with anti-bovine IRBP have Mr grouped between 124,000 and 144,000 in amphibians, reptiles, birds and mammals. Two species of teleost fish had a similar immunoreactive protein in their IPM, but the Mr was about half that of the other species, i.e. 67,000.

Original languageEnglish (US)
Pages (from-to)1581-1594
Number of pages14
JournalVision Research
Volume24
Issue number11
DOIs
StatePublished - Jan 1 1984

Fingerprint

Retinol-Binding Proteins
Retinoids
Vitamin A
Retina
Cytosol
Rod Cell Outer Segment
Ependymoglial Cells
Rhodopsin
Epithelium
Proteins
Regeneration
Cellular Retinol-Binding Proteins
Retinaldehyde
Dark Adaptation
Reptiles
Membranes
Retinal Pigment Epithelium
Amphibians
Lighting
Birds

Keywords

  • Retina
  • Retinal
  • Retinal pigment epithelium
  • Retinoid
  • Retinoid-binding proteins
  • Retinol
  • Retinyl palmitate
  • Rhodopsin
  • Visual cycle

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems

Cite this

Bridges, C. D. B., Alvarez, R. A., Fong, S. L., Gonzalez-Fernandez, F., Lam, D. M. K., & Liou, G. I. (1984). Visual cycle in the mammalian eye. Retinoid-binding proteins and the distribution of 11-cis retinoids. Vision Research, 24(11), 1581-1594. https://doi.org/10.1016/0042-6989(84)90316-X

Visual cycle in the mammalian eye. Retinoid-binding proteins and the distribution of 11-cis retinoids. / Bridges, C. D.B.; Alvarez, R. A.; Fong, S. L.; Gonzalez-Fernandez, F.; Lam, D. M.K.; Liou, Gregory I.

In: Vision Research, Vol. 24, No. 11, 01.01.1984, p. 1581-1594.

Research output: Contribution to journalArticle

Bridges, CDB, Alvarez, RA, Fong, SL, Gonzalez-Fernandez, F, Lam, DMK & Liou, GI 1984, 'Visual cycle in the mammalian eye. Retinoid-binding proteins and the distribution of 11-cis retinoids', Vision Research, vol. 24, no. 11, pp. 1581-1594. https://doi.org/10.1016/0042-6989(84)90316-X
Bridges CDB, Alvarez RA, Fong SL, Gonzalez-Fernandez F, Lam DMK, Liou GI. Visual cycle in the mammalian eye. Retinoid-binding proteins and the distribution of 11-cis retinoids. Vision Research. 1984 Jan 1;24(11):1581-1594. https://doi.org/10.1016/0042-6989(84)90316-X
Bridges, C. D.B. ; Alvarez, R. A. ; Fong, S. L. ; Gonzalez-Fernandez, F. ; Lam, D. M.K. ; Liou, Gregory I. / Visual cycle in the mammalian eye. Retinoid-binding proteins and the distribution of 11-cis retinoids. In: Vision Research. 1984 ; Vol. 24, No. 11. pp. 1581-1594.
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abstract = "This work was designed to provide an insight into the mammalian visual cycle by investigating the possible function of retinoid-binding proteins in this system, and the distribution and type of 11-cis retinoids present in the interphotoreceptor matrix and the cytosols of the retinal pigment epithelium and retina. The total retinol and retinal in the soluble fractions from these three compartments was 8{\%} (3.31 nmol/eye) of the retinyl palmitate and stearate stored in the pigment epithelium membrane fractions (39 nmol/eye). Only small amounts of retinoids were detected in the rod outer segment cytosol. The insoluble fractions also contained retinol, nearly all of which was found in the retina. The retinoids in the soluble fractions appeared to be bound to cellular retinol-binding protein (CRBP), cellular retinal-binding protein (CRA1BP) and interstitial retinol-binding protein (IRBP, a high-Mr glycoprotein). Using immunospecific precipitation, immunoblot and immunocytochemical techniques it was demonstrated that IRBP was localized in the interphotoreceptor matrix and was synthesized and secreted by the retina, a process that did not require the protein to be glycosylated. The amount of retinol bound to IRBP increased if the eyes were exposed to light, when it was estimated that the protein carried up to 30{\%} of its full capacity for all-trans retinol. In addition to all-trans retinol, IRBP carried smaller amounts of 11-cis retinol. The proportion of 11-cis retinol was frequently higher in eyes that had been protected from illumination, suggesting that IRBP plays a role in rhodopsin regeneration during dark-adaptation. Additionally, endogenous 11-cis retinoids in the retina and RPE cytosols were bound to an Mr 33,000 protein tentatively identified as CRA1BP. The 11-cis retinoid in the retina cytosol was mainly in the form of retinol, while in the RPE cytosol it was mainly in the form of retinal. Substantial amounts of 11-cis retinol were also found in the insoluble (membrane) fraction from the retina. It is suggested that in the mammalian retina 11-cis retinol is generated from all-trans retinol (possibly in the Muller cells). Lack of an 11-cis retinol oxidoreductase in the retina prevents it from being utilized for rhodopsin regeneration until it has been transported to the pigment epithelium, where it is converted to 11-cis retinal and returned to the rod outer segments. It is also suggested that IRBP may be implicated in the transport of retinoids between the rod outer segments, the Muller cells and the pigment epithelium. Proteins that are immunoreactive with anti-bovine IRBP have Mr grouped between 124,000 and 144,000 in amphibians, reptiles, birds and mammals. Two species of teleost fish had a similar immunoreactive protein in their IPM, but the Mr was about half that of the other species, i.e. 67,000.",
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T1 - Visual cycle in the mammalian eye. Retinoid-binding proteins and the distribution of 11-cis retinoids

AU - Bridges, C. D.B.

AU - Alvarez, R. A.

AU - Fong, S. L.

AU - Gonzalez-Fernandez, F.

AU - Lam, D. M.K.

AU - Liou, Gregory I

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N2 - This work was designed to provide an insight into the mammalian visual cycle by investigating the possible function of retinoid-binding proteins in this system, and the distribution and type of 11-cis retinoids present in the interphotoreceptor matrix and the cytosols of the retinal pigment epithelium and retina. The total retinol and retinal in the soluble fractions from these three compartments was 8% (3.31 nmol/eye) of the retinyl palmitate and stearate stored in the pigment epithelium membrane fractions (39 nmol/eye). Only small amounts of retinoids were detected in the rod outer segment cytosol. The insoluble fractions also contained retinol, nearly all of which was found in the retina. The retinoids in the soluble fractions appeared to be bound to cellular retinol-binding protein (CRBP), cellular retinal-binding protein (CRA1BP) and interstitial retinol-binding protein (IRBP, a high-Mr glycoprotein). Using immunospecific precipitation, immunoblot and immunocytochemical techniques it was demonstrated that IRBP was localized in the interphotoreceptor matrix and was synthesized and secreted by the retina, a process that did not require the protein to be glycosylated. The amount of retinol bound to IRBP increased if the eyes were exposed to light, when it was estimated that the protein carried up to 30% of its full capacity for all-trans retinol. In addition to all-trans retinol, IRBP carried smaller amounts of 11-cis retinol. The proportion of 11-cis retinol was frequently higher in eyes that had been protected from illumination, suggesting that IRBP plays a role in rhodopsin regeneration during dark-adaptation. Additionally, endogenous 11-cis retinoids in the retina and RPE cytosols were bound to an Mr 33,000 protein tentatively identified as CRA1BP. The 11-cis retinoid in the retina cytosol was mainly in the form of retinol, while in the RPE cytosol it was mainly in the form of retinal. Substantial amounts of 11-cis retinol were also found in the insoluble (membrane) fraction from the retina. It is suggested that in the mammalian retina 11-cis retinol is generated from all-trans retinol (possibly in the Muller cells). Lack of an 11-cis retinol oxidoreductase in the retina prevents it from being utilized for rhodopsin regeneration until it has been transported to the pigment epithelium, where it is converted to 11-cis retinal and returned to the rod outer segments. It is also suggested that IRBP may be implicated in the transport of retinoids between the rod outer segments, the Muller cells and the pigment epithelium. Proteins that are immunoreactive with anti-bovine IRBP have Mr grouped between 124,000 and 144,000 in amphibians, reptiles, birds and mammals. Two species of teleost fish had a similar immunoreactive protein in their IPM, but the Mr was about half that of the other species, i.e. 67,000.

AB - This work was designed to provide an insight into the mammalian visual cycle by investigating the possible function of retinoid-binding proteins in this system, and the distribution and type of 11-cis retinoids present in the interphotoreceptor matrix and the cytosols of the retinal pigment epithelium and retina. The total retinol and retinal in the soluble fractions from these three compartments was 8% (3.31 nmol/eye) of the retinyl palmitate and stearate stored in the pigment epithelium membrane fractions (39 nmol/eye). Only small amounts of retinoids were detected in the rod outer segment cytosol. The insoluble fractions also contained retinol, nearly all of which was found in the retina. The retinoids in the soluble fractions appeared to be bound to cellular retinol-binding protein (CRBP), cellular retinal-binding protein (CRA1BP) and interstitial retinol-binding protein (IRBP, a high-Mr glycoprotein). Using immunospecific precipitation, immunoblot and immunocytochemical techniques it was demonstrated that IRBP was localized in the interphotoreceptor matrix and was synthesized and secreted by the retina, a process that did not require the protein to be glycosylated. The amount of retinol bound to IRBP increased if the eyes were exposed to light, when it was estimated that the protein carried up to 30% of its full capacity for all-trans retinol. In addition to all-trans retinol, IRBP carried smaller amounts of 11-cis retinol. The proportion of 11-cis retinol was frequently higher in eyes that had been protected from illumination, suggesting that IRBP plays a role in rhodopsin regeneration during dark-adaptation. Additionally, endogenous 11-cis retinoids in the retina and RPE cytosols were bound to an Mr 33,000 protein tentatively identified as CRA1BP. The 11-cis retinoid in the retina cytosol was mainly in the form of retinol, while in the RPE cytosol it was mainly in the form of retinal. Substantial amounts of 11-cis retinol were also found in the insoluble (membrane) fraction from the retina. It is suggested that in the mammalian retina 11-cis retinol is generated from all-trans retinol (possibly in the Muller cells). Lack of an 11-cis retinol oxidoreductase in the retina prevents it from being utilized for rhodopsin regeneration until it has been transported to the pigment epithelium, where it is converted to 11-cis retinal and returned to the rod outer segments. It is also suggested that IRBP may be implicated in the transport of retinoids between the rod outer segments, the Muller cells and the pigment epithelium. Proteins that are immunoreactive with anti-bovine IRBP have Mr grouped between 124,000 and 144,000 in amphibians, reptiles, birds and mammals. Two species of teleost fish had a similar immunoreactive protein in their IPM, but the Mr was about half that of the other species, i.e. 67,000.

KW - Retina

KW - Retinal

KW - Retinal pigment epithelium

KW - Retinoid

KW - Retinoid-binding proteins

KW - Retinol

KW - Retinyl palmitate

KW - Rhodopsin

KW - Visual cycle

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