Component
Cellular retinaldehyde-binding protein / CRALBP
RLBP1 product binding cis-retinoids; same canonical protein in RPE and Müller glia.
4 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
CRALBP coexpression increased 11-cis-retinol production approximately threefold in homogenates of cells stably expressing chicken DES1.
Experimental context and source evidence
- cross_nutrient
- false
- evidence_location
- Figure 5b
- experimental_model
- Chicken CRALBP transfection into stable DES1-expressing 293T cells
- exposure
- All-trans-retinol substrate; CRALBP plasmid versus empty-vector comparison.
- limitations
- An assay yield effect does not prove physiological transport or human supplementation benefit.
- 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
- Gallus gallus proteins in Homo sapiens cells
- plain_language
- The binding protein shifted the measured output toward the visual-cycle alcohol.
- primary_references
- [vav-kaylor2013] Identification of DES1 as a vitamin A isomerase in Müller glial cells of the retina. (2013). https://pubmed.ncbi.nlm.nih.gov/23143414/ DOI: 10.1038/nchembio.1114
- tissue_or_cell_type
- cell homogenates
Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 573–586
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Chicken CRALBP transfection into stable DES1-expressing 293T cells · source_derived_draft · unverified_draft
### vae-cralbp-des1-isomer-yield CRALBP coexpression increased 11-cis-retinol production approximately threefold in homogenates of cells stably expressing chicken DES1. Condition category: normal nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: The binding protein shifted the measured output toward the visual-cycle alcohol. organism: Gallus gallus proteins in Homo sapiens cells tissue_or_cell_type: cell homogenates experimental_model: Chicken CRALBP transfection into stable DES1-expressing 293T cells limitations: An assay yield effect does not prove physiological transport or human supplementation benefit. exposure: All-trans-retinol substrate; CRALBP plasmid versus empty-vector comparison. cross_nutrient: false evidence_location: Figure 5b nutrient: Vitamin A [vav-kaylor2013] Identification of DES1 as a vitamin A isomerase in Müller glial cells of the retina. (2013). https://pubmed.ncbi.nlm.nih.gov/23143414/ DOI: 10.1038/nchembio.1114
Complete structured claim and evidenceAdding 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 evidenceMüller-cell-directed CRALBP restoration in Rlbp1-null/Gnat1-null mice improved cone recovery in the isolated-retina paradigm.
Experimental context and source evidence
- experimental_model
- Cell-directed AAV rescue; ex vivo cone ERG
- intervention
- AAV protein restoration in genetic knockout
- limitations
- Rescue from global deletion is not equivalent to deleting only Müller CRALBP in an intact eye.
- nutrient_topic
- Vitamin A research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Mus musculus
- plain_language
- Müller-cell CRALBP can support a retinal route for cone pigment renewal.
- primary_references
- [xue-2015] CRALBP supports the mammalian retinal visual cycle and cone vision (2015). https://pmc.ncbi.nlm.nih.gov/articles/PMC4319437/ DOI: 10.1172/JCI79651
- tissue_or_cell_type
- Müller glia and cone retina
Vitamin A: forms, mechanisms, deficiency and excess (2026-09-17) · lines 882–892
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Cell-directed AAV rescue; ex vivo cone ERG · source_derived_draft · unverified_draft
### a-vision-muller-cralbp-cones Müller-cell-directed CRALBP restoration in Rlbp1-null/Gnat1-null mice improved cone recovery in the isolated-retina paradigm. Condition category: normal nutrient_topic: Vitamin A research collection; topical membership is not evidence of a direct dietary effect. plain_language: Müller-cell CRALBP can support a retinal route for cone pigment renewal. organism: Mus musculus tissue_or_cell_type: Müller glia and cone retina experimental_model: Cell-directed AAV rescue; ex vivo cone ERG limitations: Rescue from global deletion is not equivalent to deleting only Müller CRALBP in an intact eye. intervention: AAV protein restoration in genetic knockout [xue-2015] CRALBP supports the mammalian retinal visual cycle and cone vision (2015). https://pmc.ncbi.nlm.nih.gov/articles/PMC4319437/ DOI: 10.1172/JCI79651
Complete structured claim and evidence
Where it participates (unsigned role)
RPE-selective CRALBP deletion slowed bulk visual chromophore regeneration approximately 15-fold in mice.
Experimental context and source evidence
- availability_state
- machinery_impairment Imported condition classification; unverified.
- experimental_model
- Timed RPE-selective knockout; post-bleach HPLC
- limitations
- Bulk recovery mainly reflects rods; not a direct human effect size.
- nutrient_topic
- Vitamin A research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
- organism
- Mus musculus
- plain_language
- RPE CRALBP strongly supports replenishment of cis retinal.
- primary_references
- [bassetto-2024] Dominant role for pigment epithelial CRALBP in supplying visual chromophore to photoreceptors (2024). https://pubmed.ncbi.nlm.nih.gov/38676924/ DOI: 10.1016/j.celrep.2024.114143
- tissue_or_cell_type
- RPE/whole-eye retinoids
- trigger_kind
- machinery_impairment Imported condition classification; unverified.
Vitamin A: forms, mechanisms, deficiency and excess (2026-09-17) · lines 860–869
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Timed RPE-selective knockout; post-bleach HPLC · source_derived_draft · unverified_draft
### a-vision-rpe-cralbp-chromophore RPE-selective CRALBP deletion slowed bulk visual chromophore regeneration approximately 15-fold in mice. Condition category: machinery_impairment nutrient_topic: Vitamin A research collection; topical membership is not evidence of a direct dietary effect. plain_language: RPE CRALBP strongly supports replenishment of cis retinal. organism: Mus musculus tissue_or_cell_type: RPE/whole-eye retinoids experimental_model: Timed RPE-selective knockout; post-bleach HPLC limitations: Bulk recovery mainly reflects rods; not a direct human effect size. [bassetto-2024] Dominant role for pigment epithelial CRALBP in supplying visual chromophore to photoreceptors (2024). https://pubmed.ncbi.nlm.nih.gov/38676924/ DOI: 10.1016/j.celrep.2024.114143
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.