Evidence map›Paper›PMID 23887690›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

Determination of mesenchymal stem cell fate by pigment epithelium-derived factor (PEDF) results in increased adiposity and reduced bone mineral content.

Arijeet K Gattu, E Scott Swenson, Yasuko Iwakiri, Varman T Samuel, Nancy Troiano, Ryan Berry, Christopher D Church, Matthew S Rodeheffer, Thomas O Carpenter, Chuhan Chung

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 77 citations in OpenAlex.

  1. Trial
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  6. Osteogenesis imperfecta: pathogenesis, classification, and treatment.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
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  12. Antagonism Between PEDF and TGF-β Contributes to Type VI Osteogenesis Imperfecta Bone and Vascular Pathogenesis.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  13. Review
  14. Article
  15. Review
  16. Observational
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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

10 authors at 2 institutions in 1 country.

Arijeet K Gattu1Section of Digestive Diseases, Department of Medicine, Yale University School of Medicine, 1080 LMP, New Haven, CT, USA. chuhan.chung@yale.edu.
E Scott Swenson
Yasuko Iwakiri
Varman T Samuel
Nancy Troiano
Ryan Berry
Christopher D Church
Matthew S Rodeheffer
Thomas O Carpenter
Chuhan Chung
Yale University · USVA Connecticut Healthcare System · US

Funding

Yale Liver CenterP30DK034989 · NIDDK · YALE UNIVERSITY · PI YASUKO IWAKIRI · 1986 to 2026
$31.1M
YALE CORE CENTER FOR MUSCULOSKELETAL DISORDERSP30AR046032 · NIAMS · YALE UNIVERSITY · PI HOROWITZ, MARK C · 1999 to 2013
$9.0M
Cellular & molecular mechanisms of white adipose tissue mass regulationR01DK090489 · NIDDK · YALE UNIVERSITY · PI RODEHEFFER, MATTHEW S · 2011 to 2020
$3.8M
Arterial Remodeling in Chronic Liver DiseasesR01DK082600 · NIDDK · YALE UNIVERSITY · PI IWAKIRI, YASUKO · 2009 to 2014
$2.0M
NIAMS NIH HHS P30 AR046032NIAMS NIH HHS P30-AR46032NIDDK NIH HHS DK082600NIDDK NIH HHS DK34989NIDDK NIH HHS P30 DK034989NIDDK NIH HHS R01 DK082600NIDDK NIH HHS R01 DK090489
6 · The paper itself

Abstract

Pigment epithelium-derived factor (PEDF), the protein product of the SERPINF1 gene, has been linked to distinct diseases involving adipose or bone tissue, the metabolic syndrome, and osteogenesis imperfecta (OI) type VI. Since mesenchymal stem cell (MSC) differentiation into adipocytes vs. osteoblasts can be regulated by specific factors, PEDF-directed dependency of murine and human MSCs was assessed. PEDF inhibited adipogenesis and promoted osteoblast differentiation of murine MSCs, osteoblast precursors, and human MSCs. Blockade of adipogenesis by PEDF suppressed peroxisome proliferator-activated receptor-γ (PPARγ), adiponectin, and other adipocyte markers by nearly 90% compared with control-treated cells (P<0.001). Differentiation to osteoblasts by PEDF resulted in a common pathway that involved PPARγ suppression (P<0.01). Canonical Wnt-β-catenin signaling results in a MSC differentiation pattern analogous to that seen with PEDF. Thus, adding PEDF enhanced Wnt-β-catenin signal transduction in human MSCs, demonstrating a novel Wnt agonist function. In PEDF knockout (KO) mice, total body adiposity was increased by >50% compared with controls, illustrating its systemic role as a negative regulator of adipogenesis. Bones from KO mice demonstrated a reduction in mineral content recapitulating the OI type VI phenotype. These results demonstrate that the human diseases associated with PEDF reflect its ability to modulate MSC differentiation.

Indexed as

AdipogenesisAdiposityBone DensityAdipocytesAdiponectinAnimalsCell LineCells, CulturedEye ProteinsHumansMesenchymal Stem CellsMiceMice, KnockoutNerve Growth FactorsOsteoblastsPigment Epithelium-Derived FactorAdiponectinEye ProteinsNerve Growth FactorsPigment Epithelium-Derived FactorPPAR gammaSerpinsWnt Proteinsmetabolic syndromeosteogenesis imperfecta type VI

Identifiers

PMID23887690
PMCPMC3804749
OpenAlexW2140907695

What OpenQuestion holds

Textmetadata
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.