Evidence map›Paper›PMID 26287732›Full record

ArticlePloS one2015

TNF Induction of NF-κB RelB Enhances RANKL-Induced Osteoclastogenesis by Promoting Inflammatory Macrophage Differentiation but also Limits It through Suppression of NFATc1 Expression.

Zhijun Zhao, Xiaodong Hou, Xiaoxiang Yin, Yanyun Li, Rong Duan, Brendan F Boyce, Zhenqiang Yao

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
1.7field-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

43 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Article
  3. Synergistic roles of NFATc1 and c-Jun in immunomodulation.Biochemistry and biophysics reports · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Induction of the humanMolecular medicine reports · 2024
    Article
  10. Article
  11. Role and Regulation of Transcription Factors in Osteoclastogenesis.International journal of molecular sciences · 2023
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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

7 authors at 2 institutions in 2 countries.

Zhijun ZhaoDepartment of Medical Imaging, Henan University First Affiliated Hospital, 357 Ximen Street, Kaifeng, Henan 475001, P.R. China.
Xiaodong HouDepartment of Medical Imaging, Henan University First Affiliated Hospital, 357 Ximen Street, Kaifeng, Henan 475001, P.R. China; University of Rochester Medical Center, Department of Pathology and Laboratory Medicine and Center for Musculoskeletal Research, Box 626, Room 1-2105, 601 Elmwood Ave, Rochester, NY 14642, United States of America.
Xiaoxiang YinDepartment of Medical Imaging, Henan University First Affiliated Hospital, 357 Ximen Street, Kaifeng, Henan 475001, P.R. China; University of Rochester Medical Center, Department of Pathology and Laboratory Medicine and Center for Musculoskeletal Research, Box 626, Room 1-2105, 601 Elmwood Ave, Rochester, NY 14642, United States of America.
Yanyun LiUniversity of Rochester Medical Center, Department of Pathology and Laboratory Medicine and Center for Musculoskeletal Research, Box 626, Room 1-2105, 601 Elmwood Ave, Rochester, NY 14642, United States of America.
Rong DuanUniversity of Rochester Medical Center, Department of Pathology and Laboratory Medicine and Center for Musculoskeletal Research, Box 626, Room 1-2105, 601 Elmwood Ave, Rochester, NY 14642, United States of America.
Brendan F BoyceUniversity of Rochester Medical Center, Department of Pathology and Laboratory Medicine and Center for Musculoskeletal Research, Box 626, Room 1-2105, 601 Elmwood Ave, Rochester, NY 14642, United States of America.
Zhenqiang YaoUniversity of Rochester Medical Center, Department of Pathology and Laboratory Medicine and Center for Musculoskeletal Research, Box 626, Room 1-2105, 601 Elmwood Ave, Rochester, NY 14642, United States of America.
University of Rochester Medical Center · USFirst Affiliated Hospital of Henan University · CN

Funding

Studies on the fate of the OsteoclastR01AR043510 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI BOYCE, BRENDAN F · 1995 to 2025
$8.4M
The University of Rochester Core Center for Musculoskeletal Biology and MedicineP30AR061307 · NIAMS · UNIVERSITY OF ROCHESTER · PI SCHWARZ, EDWARD M. · 2011 to 2015
$3.0M
NIAMS NIH HHS AR43510NIAMS NIH HHS P30 AR061307NIAMS NIH HHS P30AR061307NIAMS NIH HHS R01 AR043510
6 · The paper itself

Abstract

TNF induces bone loss in common bone diseases by promoting osteoclast formation directly and indirectly, but it also limits osteoclast formation by inducing expression of NF-κB p100. Osteoclast precursors (OCPs) are derived from M1 (inflammatory) and M2 (resident) macrophages. However, it is not known if TNF stimulates or limits osteoclast formation through regulation of M1 or M2 differentiation or if RelB, a partner of p100, is involved. To investigate these questions, we treated bone marrow cells (BMCs) with M-CSF alone or in combination with TNF to enrich for OCPs, which we called M-OCPs and T-OCPs, respectively. We found that TNF switched CD11b+F4/80+ M-OCPs from Ly6C-Gr1- M2 to Ly6C+Gr1-CD11c+ and Ly6C-Gr1-CD11c+ M1 cells. RANKL induced osteoclast formation from both Ly6C+Gr1- and Ly6C-Gr1- T-OCPs, but only from Ly6C+Gr1- M-OCPs, which formed significantly fewer osteoclasts than T-OCPs. Importantly, Ly6C+Gr1- cells from both M- and T-OCPs have increased expression of the M1 marker genes, iNOS, TNF, IL-1β and TGFβ1, compared to Ly6C-Gr1- cells, and Ly6C-Gr1- cells from T-OCPs also have increased expression of iNOS and TGFβ1 compared to cells from M-OCPs. Both RANKL and TNF increased RelB mRNA expression. TNF significantly increased RelB protein levels, but RANKL did not because it also induced RelB proteasomal degradation. TNF inhibited RANKL-induced NFATc1 mRNA expression and osteoclast formation from M-OCPs, but not from T-OCPs, and it did not induce Ly6C+Gr1-CD11c+ or Ly6C-Gr1-CD11c+ M1 macrophages from RelB-/- BMCs. Furthermore, overexpression of RelB in M-OCPs reduced RANKL-induced osteoclast formation and NFATc1 mRNA expression, but it increased TNF-induced OC formation without affecting NFATc1 levels. Thus, TNF induction of RelB directly mediates terminal osteoclast differentiation independent of NFATc1 and limits RANKL-induced osteoclastogenesis by inhibiting NFATc1 activation. However, the dominant role of TNF is to expand the OCP pool by switching the differentiation of M-CSF-induced M2 to M1 macrophages with enhanced osteoclast forming potential. Strategies to degrade RelB could prevent TNF-induced M2/M1 switching and reduce osteoclast formation.

Indexed as

AnimalsBone Marrow CellsCell DifferentiationInflammationMacrophage Colony-Stimulating FactorMacrophagesMiceMice, Inbred C57BLNFATC Transcription FactorsNF-kappa B p52 SubunitOsteoclastsRANK LigandRNA, MessengerTranscription Factor RelBTumor Necrosis Factor-alphaMacrophage Colony-Stimulating FactorNfatc1 protein, mouseNFATC Transcription FactorsNF-kappa B p52 SubunitRANK LigandRNA, MessengerTnfsf11 protein, mouseTranscription Factor RelBTumor Necrosis Factor-alpha

Identifiers

PMID26287732
PMCPMC4545392
OpenAlexW2159992335

What OpenQuestion holds

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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.