Evidence map›Paper›PMID 12595434›Full record

ArticleInfection and immunity2003

Functional CD40 expression induced following bacterial infection of mouse and human osteoblasts.

Laura W Schrum, Ian Marriott, Betsy R Butler, Elaine K Thomas, Michael C Hudson, Kenneth L Bost

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Frontiers in cellular and infection microbiology · 2022
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. The role of recipient T cells in mesenchymal stem cell-based tissue regeneration.The international journal of biochemistry & cell biology · 2012
    Review
  10. Article
  11. Gene-gene interaction between CD40 and CD40L reduces bone mineral density and increases osteoporosis risk in women.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2011
    Article
  12. A C >T polymorphism located at position -1 of the Kozak sequence of CD40 gene is associated with low bone mass in Spanish postmenopausal women.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2008
    Article
  13. Osteoblasts express NLRP3, a nucleotide-binding domain and leucine-rich repeat region containing receptor implicated in bacterially induced cell death.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2008
    Article
  14. Article
  15. Review
  16. Article
  17. 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

6 authors at 3 institutions in 1 country.

Laura W SchrumDepartment of Biology, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, USA. lwschrum@email.uncc.edu
Ian Marriott
Betsy R Butler
Elaine K Thomas
Michael C Hudson
Kenneth L Bost
University of North Carolina at Charlotte · USIDEX Corporation (United States) · USJohnson C. Smith University · US

Funding

RESEARCH ENHANCEMENT AT JOHNSON C SMITH UNIVERSITYR25GM058042 · NIGMS · JOHNSON C. SMITH UNIVERSITY · PI CHAMPION, TIMOTHY D · 1998 to 2005
$2.8M
Bacterial infection induces cytokine productionR03AR047585 · NIAMS · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI MARRIOTT, IAN · 2001 to 2003
$163k
NIAMS NIH HHS AR47585NIGMS NIH HHS GM58042NIGMS NIH HHS R25 GM058042
6 · The paper itself

Abstract

Bacterially induced bone infections often result in significant local inflammatory responses which are coupled with loss of bone. However, the mechanisms necessary for the protective host response, or those responsible for pathogen-induced bone loss, are not clear. Recent evidence demonstrates that bacterially infected osteoblasts secrete chemokines and cytokines, suggesting that these cells may have an unappreciated role in supporting localized inflammation. In this study, mouse and human osteoblasts were investigated for their ability to express functional CD40 upon exposure to two important pathogens of bone, Staphylococcus aureus and Salmonella enterica serovar Dublin. Bacterial infection of cultured mouse or human osteoblasts resulted in increased CD40 mRNA and CD40 protein expression induced by either pathogen. Importantly, CD40 expression by osteoblasts was functional, as assessed by ligation of this molecule with recombinant, soluble CD154. CD40 activity was assessed by induction of interleukin-6 and granulocyte-macrophage colony-stimulating factor in osteoblasts following ligation. Cocultures of activated CD4(+) T lymphocytes and osteoblasts could interact via CD40 and CD154, since an antibody against CD40 could block macrophage inflammatory protein-1alpha secretion. Taken together, these studies conclusively demonstrate that infected osteoblasts can upregulate expression of functional CD40 molecules which mediate cytokine secretion. This surprising result further supports the notion that bone-forming osteoblasts can directly interact with CD154-expressing cells (i.e., T lymphocytes) and can contribute to the host response during bone infection.

Indexed as

AnimalsCD40 AntigensCD40 LigandCD4-Positive T-LymphocytesChemokine CCL4CytokinesFlow CytometryGene Expression RegulationHumansImmunohistochemistryMacrophage Inflammatory ProteinsMiceMice, Inbred BALB CMice, Inbred C57BLOsteoblastsRNA, MessengerCD40 AntigensCD40 LigandChemokine CCL4CytokinesMacrophage Inflammatory ProteinsRNA, Messenger

Identifiers

PMID12595434
PMCPMC148834
OpenAlexW2133982468

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.