Component
Retinal G protein-coupled receptor / RGR opsin
Nonvisual retinoid photoisomerase protein in ocular support cells; distinguish protein activity from Rgr gene manipulation.
10 recorded relationships. Experimental role, claim status and evidence remain attached to each record.
How nutrients influence it
Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
How nutrients reach it in more than one step
Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.
Tracing routes…
What it does
Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.
What it acts on
RGR purified from bovine RPE contained predominantly all-trans-retinal as its endogenous dark-state chromophore.
Experimental context and source evidence
- cross_nutrient
- false
- evidence_location
- Abstract: endogenous retinaloxime isomers
- experimental_model
- Native RGR purification and hydroxylamine derivatization
- exposure
- Dark-handled purified protein; retinal-oxime isomers identified.
- limitations
- Abstract-limited; binding composition does not quantify whole-eye recycling.
- nutrient
- Vitamin A · Vitamin A
- nutrient_topic
- Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Bos taurus
- plain_language
- RGR carries the spent all-trans retinal isomer before light reaches it.
- primary_references
- [vav-hao1999] The endogenous chromophore of retinal G protein-coupled receptor opsin from the pigment epithelium. (1999). https://pubmed.ncbi.nlm.nih.gov/10037690/ DOI: 10.1074/jbc.274.10.6085
- tissue_or_cell_type
- retinal pigment epithelium
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 408–421
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Native RGR purification and hydroxylamine derivatization · source_derived_draft · unverified_draft
### vae-rgr-dark-chromophore RGR purified from bovine RPE contained predominantly all-trans-retinal as its endogenous dark-state chromophore. Condition category: normal nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: RGR carries the spent all-trans retinal isomer before light reaches it. organism: Bos taurus tissue_or_cell_type: retinal pigment epithelium experimental_model: Native RGR purification and hydroxylamine derivatization limitations: Abstract-limited; binding composition does not quantify whole-eye recycling. exposure: Dark-handled purified protein; retinal-oxime isomers identified. cross_nutrient: false evidence_location: Abstract: endogenous retinaloxime isomers nutrient: Vitamin A [vav-hao1999] The endogenous chromophore of retinal G protein-coupled receptor opsin from the pigment epithelium. (1999). https://pubmed.ncbi.nlm.nih.gov/10037690/ DOI: 10.1074/jbc.274.10.6085
Complete structured claim and evidenceAfter photoisomerization in native bovine RPE microsomes, the RGR 11-cis-retinylidene Schiff base hydrolyzed with an estimated 7.5-second half-life at 20 degrees Celsius.
Experimental context and source evidence
- cross_nutrient
- false
- evidence_location
- Figure 1D-F; STAR Methods: hydrolysis kinetics
- experimental_model
- LC-MS/MS and retinoid analysis of native microsomes
- exposure
- 20 micromolar all-trans-retinal; 10-second 530-nm exposure, followed by dark incubation at 20 degrees Celsius.
- limitations
- Temperature-specific membrane kinetics do not directly specify a human whole-eye rate.
- nutrient
- Vitamin A · Vitamin A
- nutrient_topic
- Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Bos taurus
- plain_language
- RGR released regenerated retinal within seconds in the membrane preparation.
- primary_references
- [vav-tworak2023] Rapid RGR-dependent visual pigment recycling is mediated by the RPE and specialized Müller glia. (2023). https://pubmed.ncbi.nlm.nih.gov/37585292/ DOI: 10.1016/j.celrep.2023.112982
- tissue_or_cell_type
- RPE microsomes
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 498–511
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · LC-MS/MS and retinoid analysis of native microsomes · source_derived_draft · unverified_draft
### vae-rgr-photoproduct-release After photoisomerization in native bovine RPE microsomes, the RGR 11-cis-retinylidene Schiff base hydrolyzed with an estimated 7.5-second half-life at 20 degrees Celsius. Condition category: normal nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: RGR released regenerated retinal within seconds in the membrane preparation. organism: Bos taurus tissue_or_cell_type: RPE microsomes experimental_model: LC-MS/MS and retinoid analysis of native microsomes limitations: Temperature-specific membrane kinetics do not directly specify a human whole-eye rate. exposure: 20 micromolar all-trans-retinal; 10-second 530-nm exposure, followed by dark incubation at 20 degrees Celsius. cross_nutrient: false evidence_location: Figure 1D-F; STAR Methods: hydrolysis kinetics nutrient: Vitamin A [vav-tworak2023] Rapid RGR-dependent visual pigment recycling is mediated by the RPE and specialized Müller glia. (2023). https://pubmed.ncbi.nlm.nih.gov/37585292/ DOI: 10.1016/j.celrep.2023.112982
Complete structured claim and evidenceHEK293T cells coexpressing bovine RGR and RDH10 generated more 11-cis-retinol from all-trans-retinol during illumination than cells expressing either protein alone.
Experimental context and source evidence
- cross_nutrient
- false
- evidence_location
- Figure 1A; STAR Methods: Expression of RGR and RDH10
- experimental_model
- Recombinant bovine RGR/RDH10 coexpression
- exposure
- 30-minute illumination; 5 micromolar all-trans-retinol; assay medium contained 250 micromolar NADPH.
- limitations
- Coupled output does not prove every proposed intermediate reaction or RDH10 necessity in intact retina. Added NADPH is an assay component, not a demonstrated dietary requirement.
- nutrient
- Vitamin A · Vitamin A
- nutrient_topic
- Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Bos taurus proteins in Homo sapiens cells
- plain_language
- The two proteins supported light-dependent retinol recycling together in cultured cells.
- primary_references
- [vav-morshedian2019] Light-Driven Regeneration of Cone Visual Pigments through a Mechanism Involving RGR Opsin in Müller Glial Cells. (2019). https://pubmed.ncbi.nlm.nih.gov/31056353/ DOI: 10.1016/j.neuron.2019.04.004
- tissue_or_cell_type
- HEK293T culture
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 468–481
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Recombinant bovine RGR/RDH10 coexpression · source_derived_draft · unverified_draft
### vae-rgr-rdh10-coupled-retinol HEK293T cells coexpressing bovine RGR and RDH10 generated more 11-cis-retinol from all-trans-retinol during illumination than cells expressing either protein alone. Condition category: normal nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: The two proteins supported light-dependent retinol recycling together in cultured cells. organism: Bos taurus proteins in Homo sapiens cells tissue_or_cell_type: HEK293T culture experimental_model: Recombinant bovine RGR/RDH10 coexpression limitations: Coupled output does not prove every proposed intermediate reaction or RDH10 necessity in intact retina. Added NADPH is an assay component, not a demonstrated dietary requirement. exposure: 30-minute illumination; 5 micromolar all-trans-retinol; assay medium contained 250 micromolar NADPH. cross_nutrient: false evidence_location: Figure 1A; STAR Methods: Expression of RGR and RDH10 nutrient: Vitamin A [vav-morshedian2019] Light-Driven Regeneration of Cone Visual Pigments through a Mechanism Involving RGR Opsin in Müller Glial Cells. (2019). https://pubmed.ncbi.nlm.nih.gov/31056353/ DOI: 10.1016/j.neuron.2019.04.004
Complete structured claim and evidence
Where it participates (unsigned role)
Adding native CRALBP increased the accumulation of light-generated 11-cis-retinal in bovine RPE microsomal assays compared with denatured CRALBP.
Experimental context and source evidence
- cross_nutrient
- false
- evidence_location
- Results: Impact of CRALBP on the RPE photoisomerase activity; Figure 3d
- experimental_model
- Native versus denatured CRALBP in RPE microsomes
- exposure
- 530-nm illumination; retinal substrate; Figure 3d comparison.
- limitations
- Product protection was inferred from yield; these assays do not establish supplement effects.
- nutrient
- Vitamin A · Vitamin A
- nutrient_topic
- Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Bos taurus; recombinant human CRALBP reagent
- plain_language
- The retinoid-binding protein helps retain RGR pathway product.
- primary_references
- [vav-zhang2019] Photic generation of 11-cis-retinal in bovine retinal pigment epithelium. (2019). https://pubmed.ncbi.nlm.nih.gov/31694912/ DOI: 10.1074/jbc.ra119.011169
- tissue_or_cell_type
- RPE microsomes
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 438–451
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Native versus denatured CRALBP in RPE microsomes · source_derived_draft · unverified_draft
### vae-cralbp-rgr-product-accumulation Adding native CRALBP increased the accumulation of light-generated 11-cis-retinal in bovine RPE microsomal assays compared with denatured CRALBP. Condition category: normal nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: The retinoid-binding protein helps retain RGR pathway product. organism: Bos taurus; recombinant human CRALBP reagent tissue_or_cell_type: RPE microsomes experimental_model: Native versus denatured CRALBP in RPE microsomes limitations: Product protection was inferred from yield; these assays do not establish supplement effects. exposure: 530-nm illumination; retinal substrate; Figure 3d comparison. cross_nutrient: false evidence_location: Results: Impact of CRALBP on the RPE photoisomerase activity; Figure 3d nutrient: Vitamin A [vav-zhang2019] Photic generation of 11-cis-retinal in bovine retinal pigment epithelium. (2019). https://pubmed.ncbi.nlm.nih.gov/31694912/ DOI: 10.1074/jbc.ra119.011169
Complete structured claim and evidenceIsolated Rgr-null/Gnat1-null mouse retinas lost cone flash sensitivity faster during continuous light exposure than Rgr-intact/Gnat1-null controls.
Experimental context and source evidence
- availability_state
- machinery_impairment Imported condition classification; unverified.
- cross_nutrient
- false
- evidence_location
- Figures 4-5; Results: RGR opsin contributes to cone visual function
- experimental_model
- Ex vivo cone recordings without RPE; rod transduction disabled by Gnat1 deletion
- exposure
- 505-nm background for up to 60 minutes; 10 micromolar all-trans-retinol in perfusate; 565-nm test flashes.
- limitations
- Whole-retina Rgr deletion alone does not localize the responsible cells; isolated tissue and supplied substrate differ from intact vision.
- nutrient
- Vitamin A · Vitamin A
- nutrient_topic
- Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Mus musculus
- plain_language
- Cones maintained sensitivity less well when the isolated retina lacked RGR.
- primary_references
- [vav-morshedian2019] Light-Driven Regeneration of Cone Visual Pigments through a Mechanism Involving RGR Opsin in Müller Glial Cells. (2019). https://pubmed.ncbi.nlm.nih.gov/31056353/ DOI: 10.1016/j.neuron.2019.04.004
- tissue_or_cell_type
- isolated neural retina
- trigger_kind
- machinery_impairment Imported condition classification; unverified.
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 483–496
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Ex vivo cone recordings without RPE; rod transduction disabled by Gnat1 deletion · source_derived_draft · unverified_draft
### vae-rgr-isolated-cone-sensitivity Isolated Rgr-null/Gnat1-null mouse retinas lost cone flash sensitivity faster during continuous light exposure than Rgr-intact/Gnat1-null controls. Condition category: machinery_impairment nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: Cones maintained sensitivity less well when the isolated retina lacked RGR. organism: Mus musculus tissue_or_cell_type: isolated neural retina experimental_model: Ex vivo cone recordings without RPE; rod transduction disabled by Gnat1 deletion limitations: Whole-retina Rgr deletion alone does not localize the responsible cells; isolated tissue and supplied substrate differ from intact vision. exposure: 505-nm background for up to 60 minutes; 10 micromolar all-trans-retinol in perfusate; 565-nm test flashes. cross_nutrient: false evidence_location: Figures 4-5; Results: RGR opsin contributes to cone visual function nutrient: Vitamin A [vav-morshedian2019] Light-Driven Regeneration of Cone Visual Pigments through a Mechanism Involving RGR Opsin in Müller Glial Cells. (2019). https://pubmed.ncbi.nlm.nih.gov/31056353/ DOI: 10.1016/j.neuron.2019.04.004
Complete structured claim and evidenceBovine RGR K255A produced little 11-cis-retinal under illumination despite expression comparable to wild-type RGR in HEK293S GnTI-negative cells.
Experimental context and source evidence
- availability_state
- machinery_impairment Imported condition classification; unverified.
- cross_nutrient
- false
- evidence_location
- Results/Figure 7a-c
- experimental_model
- Recombinant bovine wild-type/K255A RGR comparison
- exposure
- All-trans-retinal and 530-nm light, with CRALBP; Figure 7.
- limitations
- Construct-specific assay; K255A numbering is retained from this paper.
- nutrient
- Vitamin A · Vitamin A
- nutrient_topic
- Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Bos taurus protein in Homo sapiens cells
- plain_language
- Disrupting the retinal-binding lysine impaired the light-driven reaction.
- primary_references
- [vav-zhang2019] Photic generation of 11-cis-retinal in bovine retinal pigment epithelium. (2019). https://pubmed.ncbi.nlm.nih.gov/31694912/ DOI: 10.1074/jbc.ra119.011169
- tissue_or_cell_type
- HEK293S GnTI-negative homogenates
- trigger_kind
- machinery_impairment Imported condition classification; unverified.
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 453–466
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Recombinant bovine wild-type/K255A RGR comparison · source_derived_draft · unverified_draft
### vae-rgr-k255a-photoactivity Bovine RGR K255A produced little 11-cis-retinal under illumination despite expression comparable to wild-type RGR in HEK293S GnTI-negative cells. Condition category: machinery_impairment nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: Disrupting the retinal-binding lysine impaired the light-driven reaction. organism: Bos taurus protein in Homo sapiens cells tissue_or_cell_type: HEK293S GnTI-negative homogenates experimental_model: Recombinant bovine wild-type/K255A RGR comparison limitations: Construct-specific assay; K255A numbering is retained from this paper. exposure: All-trans-retinal and 530-nm light, with CRALBP; Figure 7. cross_nutrient: false evidence_location: Results/Figure 7a-c nutrient: Vitamin A [vav-zhang2019] Photic generation of 11-cis-retinal in bovine retinal pigment epithelium. (2019). https://pubmed.ncbi.nlm.nih.gov/31694912/ DOI: 10.1074/jbc.ra119.011169
Complete structured claim and evidenceRgrStop/Stop mice with intact Gnat1 recovered rod ERG responses more slowly after sustained bright illumination than Rgr-intact controls.
Experimental context and source evidence
- availability_state
- machinery_impairment Imported condition classification; unverified.
- cross_nutrient
- false
- evidence_location
- Figure 8A; Results: RGR supports rod dark adaptation
- experimental_model
- Transcriptional-stop Rgr knockout; rod-driven ERG
- exposure
- 530-nm background at 300 cd/m2 for 30 minutes; recovery followed in darkness.
- limitations
- Post-illumination recovery does not imply RGR catalyzes isomerization in darkness.
- nutrient
- Vitamin A · Vitamin A
- nutrient_topic
- Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Mus musculus
- plain_language
- The light-driven recycling route also helped rods recover after the light was switched off.
- primary_references
- [vav-tworak2023] Rapid RGR-dependent visual pigment recycling is mediated by the RPE and specialized Müller glia. (2023). https://pubmed.ncbi.nlm.nih.gov/37585292/ DOI: 10.1016/j.celrep.2023.112982
- tissue_or_cell_type
- intact eye; rod photoreceptors
- trigger_kind
- machinery_impairment Imported condition classification; unverified.
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 543–556
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Transcriptional-stop Rgr knockout; rod-driven ERG · source_derived_draft · unverified_draft
### vae-rgr-loss-rod-dark-adaptation RgrStop/Stop mice with intact Gnat1 recovered rod ERG responses more slowly after sustained bright illumination than Rgr-intact controls. Condition category: machinery_impairment nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: The light-driven recycling route also helped rods recover after the light was switched off. organism: Mus musculus tissue_or_cell_type: intact eye; rod photoreceptors experimental_model: Transcriptional-stop Rgr knockout; rod-driven ERG limitations: Post-illumination recovery does not imply RGR catalyzes isomerization in darkness. exposure: 530-nm background at 300 cd/m2 for 30 minutes; recovery followed in darkness. cross_nutrient: false evidence_location: Figure 8A; Results: RGR supports rod dark adaptation nutrient: Vitamin A [vav-tworak2023] Rapid RGR-dependent visual pigment recycling is mediated by the RPE and specialized Müller glia. (2023). https://pubmed.ncbi.nlm.nih.gov/37585292/ DOI: 10.1016/j.celrep.2023.112982
Complete structured claim and evidenceTamoxifen-induced Rgr reactivation through Glast-CreERT2 improved cone sensitivity during sustained light in RgrStop/Stop/Gnat1-null mice compared with untreated rescue-line controls.
Experimental context and source evidence
- availability_state
- machinery_impairment Imported condition classification; unverified.
- cross_nutrient
- false
- evidence_location
- Figure 7B; Table S1
- experimental_model
- Cell-directed excision of a floxed transcriptional stop cassette
- exposure
- 530-nm background at 300 cd/m2 for 60 minutes; cone b-wave sensitivity.
- limitations
- Each cellular rescue was partial; native relative contributions need not match other species.
- nutrient
- Vitamin A · Vitamin A
- nutrient_topic
- Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Mus musculus
- plain_language
- Restoring RGR in Müller glia helped cones respond during prolonged light.
- primary_references
- [vav-tworak2023] Rapid RGR-dependent visual pigment recycling is mediated by the RPE and specialized Müller glia. (2023). https://pubmed.ncbi.nlm.nih.gov/37585292/ DOI: 10.1016/j.celrep.2023.112982
- tissue_or_cell_type
- Müller glia; intact-eye ERG
- trigger_kind
- machinery_impairment Imported condition classification; unverified.
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 528–541
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Cell-directed excision of a floxed transcriptional stop cassette · source_derived_draft · unverified_draft
### vae-rgr-muller-rescue-cones Tamoxifen-induced Rgr reactivation through Glast-CreERT2 improved cone sensitivity during sustained light in RgrStop/Stop/Gnat1-null mice compared with untreated rescue-line controls. Condition category: machinery_impairment nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: Restoring RGR in Müller glia helped cones respond during prolonged light. organism: Mus musculus tissue_or_cell_type: Müller glia; intact-eye ERG experimental_model: Cell-directed excision of a floxed transcriptional stop cassette limitations: Each cellular rescue was partial; native relative contributions need not match other species. exposure: 530-nm background at 300 cd/m2 for 60 minutes; cone b-wave sensitivity. cross_nutrient: false evidence_location: Figure 7B; Table S1 nutrient: Vitamin A [vav-tworak2023] Rapid RGR-dependent visual pigment recycling is mediated by the RPE and specialized Müller glia. (2023). https://pubmed.ncbi.nlm.nih.gov/37585292/ DOI: 10.1016/j.celrep.2023.112982
Complete structured claim and evidenceIlluminating native bovine RGR converted its bound all-trans-retinal stereospecifically to the 11-cis configuration.
Experimental context and source evidence
- cross_nutrient
- false
- evidence_location
- Abstract: irradiation and isomer analysis
- experimental_model
- Purified native RGR photochemistry
- exposure
- 470-nm monochromatic or near-UV irradiation; duration absent from the abstract.
- limitations
- Abstract-limited; the finding does not establish relative flux in living human eyes.
- nutrient
- Vitamin A · Vitamin A
- nutrient_topic
- Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Bos taurus
- plain_language
- Light lets RGR reverse the retinal isomer change used in visual pigments.
- primary_references
- [vav-hao1999] The endogenous chromophore of retinal G protein-coupled receptor opsin from the pigment epithelium. (1999). https://pubmed.ncbi.nlm.nih.gov/10037690/ DOI: 10.1074/jbc.274.10.6085
- tissue_or_cell_type
- RPE-derived protein
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 423–436
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Purified native RGR photochemistry · source_derived_draft · unverified_draft
### vae-rgr-photoisomerization Illuminating native bovine RGR converted its bound all-trans-retinal stereospecifically to the 11-cis configuration. Condition category: normal nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: Light lets RGR reverse the retinal isomer change used in visual pigments. organism: Bos taurus tissue_or_cell_type: RPE-derived protein experimental_model: Purified native RGR photochemistry limitations: Abstract-limited; the finding does not establish relative flux in living human eyes. exposure: 470-nm monochromatic or near-UV irradiation; duration absent from the abstract. cross_nutrient: false evidence_location: Abstract: irradiation and isomer analysis nutrient: Vitamin A [vav-hao1999] The endogenous chromophore of retinal G protein-coupled receptor opsin from the pigment epithelium. (1999). https://pubmed.ncbi.nlm.nih.gov/10037690/ DOI: 10.1074/jbc.274.10.6085
Complete structured claim and evidenceTamoxifen-induced Rgr reactivation through Rpe65-CreERT2 improved cone sensitivity during sustained light in RgrStop/Stop/Gnat1-null mice compared with untreated rescue-line controls.
Experimental context and source evidence
- availability_state
- machinery_impairment Imported condition classification; unverified.
- cross_nutrient
- false
- evidence_location
- Figure 7A; Table S1
- experimental_model
- Cell-directed excision of a floxed transcriptional stop cassette
- exposure
- 530-nm background at 300 cd/m2 for 60 minutes; cone b-wave sensitivity.
- limitations
- Each cellular rescue was partial; native relative contributions need not match other species.
- nutrient
- Vitamin A · Vitamin A
- nutrient_topic
- Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Mus musculus
- plain_language
- Restoring RGR in retinal pigment epithelium helped cones respond during prolonged light.
- primary_references
- [vav-tworak2023] Rapid RGR-dependent visual pigment recycling is mediated by the RPE and specialized Müller glia. (2023). https://pubmed.ncbi.nlm.nih.gov/37585292/ DOI: 10.1016/j.celrep.2023.112982
- tissue_or_cell_type
- retinal pigment epithelium; intact-eye ERG
- trigger_kind
- machinery_impairment Imported condition classification; unverified.
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 513–526
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Cell-directed excision of a floxed transcriptional stop cassette · source_derived_draft · unverified_draft
### vae-rgr-rpe-rescue-cones Tamoxifen-induced Rgr reactivation through Rpe65-CreERT2 improved cone sensitivity during sustained light in RgrStop/Stop/Gnat1-null mice compared with untreated rescue-line controls. Condition category: machinery_impairment nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: Restoring RGR in retinal pigment epithelium helped cones respond during prolonged light. organism: Mus musculus tissue_or_cell_type: retinal pigment epithelium; intact-eye ERG experimental_model: Cell-directed excision of a floxed transcriptional stop cassette limitations: Each cellular rescue was partial; native relative contributions need not match other species. exposure: 530-nm background at 300 cd/m2 for 60 minutes; cone b-wave sensitivity. cross_nutrient: false evidence_location: Figure 7A; Table S1 nutrient: Vitamin A [vav-tworak2023] Rapid RGR-dependent visual pigment recycling is mediated by the RPE and specialized Müller glia. (2023). https://pubmed.ncbi.nlm.nih.gov/37585292/ DOI: 10.1016/j.celrep.2023.112982
Complete structured claim and evidence
The events it takes part in
A mechanism often involves more than two components. These are the full events, with every participant and its role.
Situations it appears in
Low-supply and faulty-machinery situations recorded in the chapters where this component plays a part.
In the sources
Preserved passages that mention this component, quoted exactly. Open one to read it in context.
Open hypotheses
Proposed ideas that involve this component. They are labeled as hypotheses and do not change any recorded statement.
This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.