Evidence map›Paper›PMID 25299695›Full record

ArticleInternational journal of molecular sciences2014

Curcumin-induced heme oxygenase-1 expression prevents H2O2-induced cell death in wild type and heme oxygenase-2 knockout adipose-derived mesenchymal stem cells.

Niels A J Cremers, Ditte M S Lundvig, Stephanie C M van Dalen, Rik F Schelbergen, Peter L E M van Lent, Walter A Szarek, Raymond F Regan, Carine E Carels, Frank A D T G Wagener

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. HO-1 in Bone Biology: Potential Therapeutic Strategies for Osteoporosis.Frontiers in cell and developmental biology · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. CXCL12-CXCR4 Interplay Facilitates Palatal Osteogenesis in Mice.Frontiers in cell and developmental biology · 2020
    Article
  14. [Research progress in mesenchymal stem cells modified by Heme oxygenase 1].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2019
    Review
  15. Article
  16. International journal of molecular sciences · 2018
    Article
  17. Article
  18. Article
  19. [The role of glutathione in steroid induced bone marrow mesenchymal stem cells dysfunction].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2018
    Article
  20. Article
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

9 authors at 3 institutions in 3 countries.

Niels A J CremersDepartment of Orthodontics and Craniofacial Biology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, PO Box 9101, 6500 HB Nijmegen, The Netherlands. niels.cremers@radboudumc.nl.
Ditte M S LundvigDepartment of Orthodontics and Craniofacial Biology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, PO Box 9101, 6500 HB Nijmegen, The Netherlands. ditte.lundvig@radboudumc.nl.
Stephanie C M van DalenDepartment of Rheumatology, Experimental Rheumatology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, PO Box 9101, 6500 HB Nijmegen, The Netherlands. stephanie.vandalen@radboudumc.nl.
Rik F SchelbergenDepartment of Rheumatology, Experimental Rheumatology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, PO Box 9101, 6500 HB Nijmegen, The Netherlands. rik.schelbergen@radboudumc.nl.
Peter L E M van LentDepartment of Rheumatology, Experimental Rheumatology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, PO Box 9101, 6500 HB Nijmegen, The Netherlands. peter.vanlent@radboudumc.nl.
Walter A SzarekDepartment of Chemistry, Queen's University, Kingston, ON K7L 3N6, Canada. szarekw@chem.queensu.ca.
Raymond F ReganDepartment of Emergency Medicine, Thomas Jefferson University, Philadelphia, PA 19107, USA. Raymond.regan@jefferson.edu.
Carine E CarelsDepartment of Orthodontics and Craniofacial Biology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, PO Box 9101, 6500 HB Nijmegen, The Netherlands. carine.carels@radboudumc.nl.
Frank A D T G WagenerDepartment of Orthodontics and Craniofacial Biology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, PO Box 9101, 6500 HB Nijmegen, The Netherlands. frank.wagener@radboudumc.nl.
Radboud University Nijmegen · NLQueen's University · CAThomas Jefferson University · US

Funding

Protective Effect of Hemin Preconditioning after Intracerebral HemorrhageR01NS079500 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI REGAN, RAYMOND F · 2012 to 2015
$1.3M
NINDS NIH HHS R01 NS079500
6 · The paper itself

Abstract

Mesenchymal stem cell (MSC) administration is a promising adjuvant therapy to treat tissue injury. However, MSC survival after administration is often hampered by oxidative stress at the site of injury. Heme oxygenase (HO) generates the cytoprotective effector molecules biliverdin/bilirubin, carbon monoxide (CO) and iron/ferritin by breaking down heme. Since HO-activity mediates anti-apoptotic, anti-inflammatory, and anti-oxidative effects, we hypothesized that modulation of the HO-system affects MSC survival. Adipose-derived MSCs (ASCs) from wild type (WT) and HO-2 knockout (KO) mice were isolated and characterized with respect to ASC marker expression. In order to analyze potential modulatory effects of the HO-system on ASC survival, WT and HO-2 KO ASCs were pre-treated with HO-activity modulators, or downstream effector molecules biliverdin, bilirubin, and CO before co-exposure of ASCs to a toxic dose of H2O2. Surprisingly, sensitivity to H2O2-mediated cell death was similar in WT and HO-2 KO ASCs. However, pre-induction of HO-1 expression using curcumin increased ASC survival after H2O2 exposure in both WT and HO-2 KO ASCs. Simultaneous inhibition of HO-activity resulted in loss of curcumin-mediated protection. Co-treatment with glutathione precursor N-Acetylcysteine promoted ASC survival. However, co-incubation with HO-effector molecules bilirubin and biliverdin did not rescue from H2O2-mediated cell death, whereas co-exposure to CO-releasing molecules-2 (CORM-2) significantly increased cell survival, independently from HO-2 expression. Summarizing, our results show that curcumin protects via an HO-1 dependent mechanism against H2O2-mediated apoptosis, and likely through the generation of CO. HO-1 pre-induction or administration of CORMs may thus form an attractive strategy to improve MSC therapy.

Indexed as

AcetylcysteineAdipose TissueAnimalsAntioxidantsApoptosisBilirubinBiliverdineCells, CulturedCurcuminHeme Oxygenase-1Heme Oxygenase (Decyclizing)Hydrogen PeroxideMesenchymal Stem CellsMiceMice, Inbred C57BLMice, KnockoutAcetylcysteineAntioxidantsBilirubinBiliverdineCurcuminHeme Oxygenase-1heme oxygenase-2Heme Oxygenase (Decyclizing)Hydrogen PeroxideOrganometallic CompoundsRNA, Messengertricarbonyldichlororuthenium (II) dimer

Identifiers

PMID25299695
PMCPMC4227200
OpenAlexW2168133216

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.