Evidence map›Paper›PMID 20108320›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2010

Rejuvenation of the inflammatory system stimulates fracture repair in aged mice.

Zhiqing Xing, Chuanyong Lu, Diane Hu, Theodore Miclau, Ralph S Marcucio

Open access · greenAbstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

62 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
  2. Murine Progeria Model Exhibits Delayed Fracture Healing With Senescent Phenotype and Dysregulated Immune Response.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2026
    Article
  3. Article
  4. Review
  5. Observational
  6. Review
  7. Article
  8. Article
  9. Review
  10. Osteoimmunology of Fracture Healing.Current osteoporosis reports · 2024
    Review
  11. Article
  12. Article
  13. Single-cell RNAseq provides insight into altered immune cell populations in human fracture nonunions.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

2 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

5 authors at 1 institution in 1 country.

Zhiqing XingDepartment of Orthopaedic Surgery, Orthopaedic Trauma Institute, University of California at San Francisco, 2550 23rd Street, Bldg. 9, Rm. 345, San Francisco, California 94110, USA.
Chuanyong Lu
Diane Hu
Theodore Miclau
Ralph S Marcucio
University of California, San Francisco · US

Funding

Biology of stable and non-stable fracture repairR01AR053645 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MICLAU, THEODORE · 2006 to 2010
$1.6M
NIAMS NIH HHS R01 AR053645NIAMS NIH HHS R01-AR053645-01
6 · The paper itself

Abstract

Age significantly reduces the regenerative capacity of the skeleton, but the underlying causes are unknown. Here, we tested whether the functional status of inflammatory cells contributes to delayed healing in aged animals. We created chimeric mice by bone marrow transplantation after lethal irradiation. In this model, chondrocytes and osteoblasts in the regenerate are derived exclusively from host cells while inflammatory cells are derived from the donor. Using this model, the inflammatory system of middle-aged mice (12 month old) was replaced by transplanted bone marrow from juvenile mice (4 weeks old), or age-matched controls. We found that the middle-aged mice receiving juvenile bone marrow had larger calluses and more bone formation during early stages and faster callus remodeling at late stages of fracture healing, indicating that inflammatory cells derived from the juvenile bone marrow accelerated bone repair in the middle-aged animals. In contrast, transplanting bone marrow from middle-aged mice to juvenile mice did not alter the process of fracture healing in juvenile mice. Thus, the roles of inflammatory cells in fracture healing may be age-related, suggesting the possibility of enhancing fracture healing in aged animals by manipulating the inflammatory system.

Indexed as

OsteogenesisRejuvenationAgingAnimalsBone Marrow CellsBone Marrow TransplantationBony CallusFracture HealingMiceTibial FracturesTransplantation Chimera

Identifiers

PMID20108320
PMCPMC2892015
OpenAlexW1968805389

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.