Evidence map›Paper›PMID 26247358›Full record

ArticlePloS one2015

Dendritic Cells Cause Bone Lesions in a New Mouse Model of Histiocytosis.

Frédéric Grosjean, Sonia Nasi, Pascal Schneider, Véronique Chobaz, Alexandra Liu, Vanessa Mordasini, Kristell Moullec, Paolo Vezzoni, Christine Lavanchy, Nathalie Busso and 2 more

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Observational
  6. Review
  7. A T Cell View of the Bone Marrow.Frontiers in immunology · 2016
    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

12 authors at 2 institutions in 2 countries.

Frédéric GrosjeanDepartment of Biochemistry CIIL, University of Lausanne, Epalinges, Switzerland.
Sonia NasiDAL, Service of Rheumatology, Laboratory of Rheumatology, University of Lausanne, CHUV, Epalinges, Switzerland.
Pascal SchneiderDepartment of Biochemistry CIIL, University of Lausanne, Epalinges, Switzerland.
Véronique ChobazDAL, Service of Rheumatology, Laboratory of Rheumatology, University of Lausanne, CHUV, Epalinges, Switzerland.
Alexandra LiuDepartment of Biochemistry CIIL, University of Lausanne, Epalinges, Switzerland.
Vanessa MordasiniDepartment of Biochemistry CIIL, University of Lausanne, Epalinges, Switzerland.
Kristell MoullecDepartment of Biochemistry CIIL, University of Lausanne, Epalinges, Switzerland.
Paolo VezzoniUOS/IRGB, Milan Unit, CNR, via Fantoli 15/16-20138 Milano, and Humanitas Research Center, Rozzano Italy.
Christine LavanchyDepartment of Biochemistry CIIL, University of Lausanne, Epalinges, Switzerland.
Nathalie BussoDAL, Service of Rheumatology, Laboratory of Rheumatology, University of Lausanne, CHUV, Epalinges, Switzerland.
Hans Acha-OrbeaDepartment of Biochemistry CIIL, University of Lausanne, Epalinges, Switzerland.
Driss EhirchiouDepartment of Biochemistry CIIL, University of Lausanne, Epalinges, Switzerland.
University of Lausanne · CHHumanitas University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Langerhans cell histiocytosis (LCH) is a rare disease caused by the clonal accumulation of dendritic Langerhans cells, which is often accompanied by osteolytic lesions. It has been reported that osteoclast-like cells play a major role in the pathogenic bone destruction seen in patients with LCH and these cells are postulated to originate from the fusion of DCs. However, due to the lack of reliable animal models the pathogenesis of LCH is still poorly understood. In this study, we have established a mouse model of histiocytosis- recapitulating human disease for osteolytic lesions seen in LCH patients. At 12 weeks after birth, severe bone lesions were observed in our multisystem histiocytosis (Mushi) model, when CD8α conventional dendritic cells (DCs) are transformed (MuTuDC) and accumulate. Most importantly, our study demonstrates that bone loss in LCH can be accounted for the transdifferentiation of MuTuDCs into functional osteoclasts both in vivo and in vitro. Moreover, we have shown that injected MuTuDCs reverse the osteopetrotic phenotype of oc/oc mice in vivo. In conclusion, our results support a crucial role of DCs in bone lesions in histiocytosis patients. Furthermore, our new model of LCH based on adoptive transfer of MuTuDC lines, leading to bone lesions within 1-2 weeks, will be an important tool for investigating the pathophysiology of this disease and ultimately for evaluating the potential of anti-resorptive drugs for the treatment of bone lesions.

Indexed as

AnimalsBone and BonesBone Density Conservation AgentsCell LineCell TransdifferentiationDendritic CellsDiphosphonatesDisease Models, AnimalHistiocytosis, Langerhans-CellHumansLangerhans CellsMiceMice, Inbred C57BLMice, TransgenicOsteoclastsOsteolysisBone Density Conservation AgentsDiphosphonatesOsteoprotegerin

Identifiers

PMID26247358
PMCPMC4527720
OpenAlexW1513401228

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Registered trials

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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.