Evidence map›Paper›PMID 22222225›Full record

ArticleThe American journal of pathology2012

Epithelial expression of the cytosolic retinoid chaperone cellular retinol binding protein II is essential for in vivo imprinting of local gut dendritic cells by lumenal retinoids.

Keely G McDonald, Matthew R Leach, Kaitlin W M Brooke, Caihong Wang, Leroy W Wheeler, Elyse K Hanly, Christopher W Rowley, Marc S Levin, Michael Wagner, Ellen Li and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
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  8. Article
  9. A novelDiscovery immunology · 2023
    Article
  10. Retinoid metabolism: new insights.Journal of molecular endocrinology · 2022
    Review
  11. Retinol-binding protein 2 (RBP2): More than just dietary retinoid uptake.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2022
    Review
  12. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Keely G McDonaldDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.
Matthew R LeachDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.
Kaitlin W M BrookeDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.
Caihong WangDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.
Leroy W WheelerDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.
Elyse K HanlyDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.
Christopher W RowleyDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.
Marc S LevinDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri; Department of Medicine, St. Louis VA Medical Center, St. Louis, Missouri.
Michael WagnerDepartment of Cell Biology, The State University of New York, Downstate Medical Center, Brooklyn, New York.
Ellen LiDepartment of Internal Medicine, The State University of New York, Stony Brook, New York.
Rodney D NewberryDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri. Electronic address: rnewberry@wustl.edu.
Washington University in St. Louis · USState University of New York · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
NUTRIENT MODULATION OF GENE EXPRESSION IN GUT ADAPTATIONR01DK050446 · NIDDK · WASHINGTON UNIVERSITY · PI LEVIN, MARC S · 1995 to 2011
$3.2M
Lymphotoxin Beta Receptor in Intestinal InflammationR01DK064798 · NIDDK · WASHINGTON UNIVERSITY · PI NEWBERRY, RODNEY D · 2005 to 2013
$2.8M
Epithelia Associated Dendritic Cells: Phenotype and FunctionR21AI083538 · NIAID · WASHINGTON UNIVERSITY · PI NEWBERRY, RODNEY D · 2009 to 2010
$415k
Two Distinct DC Subtypes are Associated with Murine Intestinal EpitheliumF32DK085941 · NIDDK · WASHINGTON UNIVERSITY · PI WHEELER, LEROY WILLIAM · 2010 to 2012
$130k
NCI NIH HHS P30 CA091842NCI NIH HHS P30-CA91842NIAID NIH HHS AI083538NIAID NIH HHS R21 AI083538NIDDK NIH HHS DK050446NIDDK NIH HHS DK064798NIDDK NIH HHS DK085941NIDDK NIH HHS F32 DK085941NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30-DK52574NIDDK NIH HHS R01 DK050446NIDDK NIH HHS R01 DK064798
6 · The paper itself

Abstract

Dendritic cells (DCs) use all-trans retinoic acid (ATRA) to promote characteristic intestinal responses, including Foxp3(+) Treg conversion, lymphocyte gut homing molecule expression, and IgA production. How this ability to generate ATRA is conferred to DCs in vivo remains largely unstudied. Here, we observed that among DCs, retinaldehyde dehydrogenase (ALDH1), which catalyzes the conversion of retinal to ATRA, was preferentially expressed by small intestine CD103(+) lamina propria (LP) DCs. Retinoids induced LP CD103(+) DCs to generate ATRA via ALDH1 activity. Either biliary or dietary retinoids were required to confer ALDH activity to LP DCs in vivo. Cellular retinol-binding protein II (CRBPII), a cytosolic retinoid chaperone that directs enterocyte retinol and retinal metabolism but is redundant to maintain serum retinol, was required to confer ALDH activity to CD103(+) LP DCs. CRBPII expression was restricted to small intestine epithelial cells, and ALDH activity in CRBPII(-/-) DCs was restored by transfer to a wild-type recipient. CD103(+) LP DCs from CRBPII(-/-) mice had a decreased capacity to promote IgA production. Moreover, CD103(+) DCs preferentially associated with the small intestine epithelium and LP CD103(+) DC ALDH activity, and the ability to promote IgA production was reduced in mice with impaired DC-epithelia associations. These findings demonstrate in vivo roles for the expression of epithelial CRBPII and lumenal retinoids to imprint local gut DCs with an intestinal phenotype.

Indexed as

Aldehyde Dehydrogenase 1 FamilyAnimalsAntigens, CDDendritic CellsImmunity, CellularImmunoglobulin AIntegrin alpha ChainsInterleukin-6Intestine, SmallIsoenzymesMiceMice, Inbred C57BLMice, Inbred StrainsPhenotypeRetinal DehydrogenaseRetinol-Binding Proteins, CellularAldehyde Dehydrogenase 1 FamilyALDH1A1 protein, mousealpha E integrinsAntigens, CDImmunoglobulin AIntegrin alpha ChainsInterleukin-6IsoenzymesRbp2 protein, mouseRetinal DehydrogenaseRetinol-Binding Proteins, CellularTretinoin

Identifiers

PMID22222225
PMCPMC3349881
OpenAlexW2096215219

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.