Evidence map›Paper›PMID 29754817›Full record

ArticleCell2018

Vitamin D Switches BAF Complexes to Protect β Cells.

Zong Wei, Eiji Yoshihara, Nanhai He, Nasun Hah, Weiwei Fan, Antonio F M Pinto, Timothy Huddy, Yuhao Wang, Brittany Ross, Gabriela Estepa and 10 more

Open access · greenAbstract read
In one paragraph

Article in Cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed, 4 pooled it
10.0field-weighted citation impact, top 1% 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

131 citing papers in PubMed, 4 syntheses or guidelines pooled it, 212 citations in OpenAlex.

  1. The role of vitamin D signalling in β cell apoptosis: a systematic review.Apoptosis : an international journal on programmed cell death · 2026
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Vitamin D and Beta Cells in Type 1 Diabetes: A Systematic Review.International journal of molecular sciences · 2022
    Pooled it
  5. Trial
  6. Trial
  7. Trial
  8. Type 1 Diabetes Mellitus Pathogenesis: Mechanisms, Early Diagnostic Strategies, and Emerging Therapeutic Approaches.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. FXR and BET signaling orchestrate to protect β cells.bioRxiv : the preprint server for biology · 2026
    Article
  14. Review
  15. Article
  16. BRD9 at the crossroads of splicing, chromatin remodeling, and hematopoiesis.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2026
    Review
  17. Engineering hypoimmune stem cell-derived beta cells.Stem cell research & therapy · 2025
    Review
  18. Review
  19. Review
  20. Article

71 more citing papers are in PubMed but not listed here.

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

20 authors at 3 institutions in 2 countries.

Zong WeiGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Eiji YoshiharaGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Nanhai HeGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Nasun HahGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Weiwei FanGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Antonio F M PintoClayton Foundation Laboratories for Peptide Biology, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Timothy HuddyGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Yuhao WangGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Brittany RossGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Gabriela EstepaGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Yang DaiGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Ning DingGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Mara H ShermanGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Sungsoon FangGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Xuan ZhaoGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Christopher LiddleStorr Liver Centre, Westmead Institute for Medical Research and Sydney Medical School, University of Sydney, Westmead Hospital, Westmead, NSW 2145, Australia.
Annette R AtkinsGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Ruth T YuGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Michael DownesGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA. Electronic address: downes@salk.edu.
Ronald M EvansGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA; Howard Hughes Medical Institute, Salk Institute for Biological Studies, La Jolla, CA 92037, USA. Electronic address: evans@salk.edu.
Salk Institute for Biological Studies · USHoward Hughes Medical Institute · USThe University of Sydney · AU

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
Yeast Genetics and Stress Response Genes-BiomedicalP42ES010337 · NIEHS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TUKEY, ROBERT H · 2000 to 2022
$69.8M
Transcriptional GenomicsP01HL088093 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WITZTUM, JOSEPH L. · 2008 to 2018
$26.4M
HORMONAL REGULATION OF MAMMALIAN GENE EXPRESSIONR37DK057978 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M · 2000 to 2019
$16.0M
Spatial Regulation of Developmental Gene ExpressionR01HL105278 · NHLBI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M · 2011 to 2019
$4.0M
Hormonal Regulation of Mammalian Gene ExpressionR01DK057978 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M · 2021 to 2024
$2.6M
A Hybrid Quadrupole-Orbitrap LC/MSS10OD021815 · OD · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI SAGHATELIAN, ALAN · 2016 to 2016
$580k
Howard Hughes Medical InstituteNCI NIH HHS P30 CA014195NHLBI NIH HHS P01 HL088093NHLBI NIH HHS R01 HL105278NIDDK NIH HHS R01 DK057978NIDDK NIH HHS R37 DK057978NIEHS NIH HHS P42 ES010337NIH HHS S10 OD021815
6 · The paper itself

Abstract

A primary cause of disease progression in type 2 diabetes (T2D) is β cell dysfunction due to inflammatory stress and insulin resistance. However, preventing β cell exhaustion under diabetic conditions is a major therapeutic challenge. Here, we identify the vitamin D receptor (VDR) as a key modulator of inflammation and β cell survival. Alternative recognition of an acetylated lysine in VDR by bromodomain proteins BRD7 and BRD9 directs association to PBAF and BAF chromatin remodeling complexes, respectively. Mechanistically, ligand promotes VDR association with PBAF to effect genome-wide changes in chromatin accessibility and enhancer landscape, resulting in an anti-inflammatory response. Importantly, pharmacological inhibition of BRD9 promotes PBAF-VDR association to restore β cell function and ameliorate hyperglycemia in murine T2D models. These studies reveal an unrecognized VDR-dependent transcriptional program underpinning β cell survival and identifies the VDR:PBAF/BAF association as a potential therapeutic target for T2D.

Indexed as

AnimalsBromodomain Containing ProteinsCalcitriolChromatin Assembly and DisassemblyChromosomal Proteins, Non-HistoneDiabetes Mellitus, ExperimentalHumansInsulinInsulin-Secreting CellsMaleMiceMice, Inbred C57BLMice, ObeseMutagenesis, Site-DirectedOxidative PhosphorylationProtein BindingBrd9 protein, mouseBromodomain Containing ProteinscalcipotrieneCalcitriolChromosomal Proteins, Non-HistoneInsulinReceptors, CalcitriolRNA, Guide, CRISPR-Cas SystemsRNA, Small InterferingSWI-SNF-B chromatin-remodeling complexTranscription FactorsVitamin DBAF complexBRD9chromatin remodelingCRISPR screeningdiabetesinflammationnuclear receptorPBAF complexVDRβ cell

Identifiers

PMID29754817
PMCPMC5987229
OpenAlexW2801592884

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.