Evidence map›Paper›PMID 31947698›Full record

ArticleInternational journal of molecular sciences2020

A Sub-Clone of RAW264.7-Cells Form Osteoclast-Like Cells Capable of Bone Resorption Faster than Parental RAW264.7 through Increased De Novo Expression and Nuclear Translocation of NFATc1.

Laia Mira-Pascual, Anh N Tran, Göran Andersson, Tuomas Näreoja, Pernilla Lång

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

5 authors at 2 institutions in 2 countries.

Laia Mira-PascualDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institutet, Alfred Nobels Allé, 8, SE-141 52 Stockholm, Sweden.
Anh N TranDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institutet, Alfred Nobels Allé, 8, SE-141 52 Stockholm, Sweden.
Göran AnderssonDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institutet, Alfred Nobels Allé, 8, SE-141 52 Stockholm, Sweden.
Tuomas NäreojaDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institutet, Alfred Nobels Allé, 8, SE-141 52 Stockholm, Sweden.ORCID 0000-0002-2174-4434
Pernilla LångDepartment of Laboratory Medicine, Division of Pathology, Karolinska Institutet, Alfred Nobels Allé, 8, SE-141 52 Stockholm, Sweden.
Karolinska Institutet · SEUniversity of Aberdeen · GB

Funding

FP7 People: Marie-Curie Actions Euroclast, FP7-People-2013-ITN:#607447Jane ja Aatos Erkon Säätiö TN/2017Loo och Hans Ostermans Stiftelse för Medicinsk Forskning TN/2018Vetenskapsrådet #2017-01083Vetenskapsrådet (K2015-99X-10363-23-4)
6 · The paper itself

Abstract

The murine macrophage cell line RAW264.7 is extensively used as a progenitor to study osteoclast (OC) differentiation. RAW264.7 is a heterogeneous cell line, containing sub-clones with different abilities to form OCs. The aim of this study was to identify characteristics within the heterogeneous RAW264.7 cells that define sub-clones with an augmented ability to form bone-resorbing OCs (H9), as well as sub-clones representing non-OCs (J8). RAW264.7 sub-clones were isolated by single cell cloning. Selection was based on TRAP/cathepsin K expression in sub-clone cultures without added RANKL. Sub-clones before and after differentiation with RANKL were assayed for multiple OC-characteristics. Sub-clone H9 cells presented a higher expression of OC-markers in cultures without added RANKL compared to the parental RAW264.7. After 6 days of RANKL stimulation, sub-clone H9 cells had equal expression levels of OC-markers with RAW264.7 and formed OCs able to demineralize hydroxyapatite. However, sub-clone H9 cells displayed rapid differentiation of OC already at Day 2 compared to Day 4 from parental RAW264.7, and when cultured on plastic and on bone they were more efficient in resorption. This rapid differentiation was likely due to high initial expression/nuclear translocation of OC master transcription factor, NFATc1. In contrast to H9, J8 cells expressed initially very low levels of OC-markers, and they did not respond to RANKL-stimulation by developing OC-characteristics/OC-marker expression. Hence, H9 is an additional clone suitable for experimental setup requiring rapid differentiation of large numbers of OCs.

Indexed as

AnimalsBone ResorptionCathepsin KCell DifferentiationCell LineCells, CulturedGene ExpressionGene Expression ProfilingGene Expression RegulationMiceNFATC Transcription FactorsOrgan SpecificityOsteoclastsRANK LigandRAW 264.7 CellsTartrate-Resistant Acid PhosphataseAcp5 protein, mouseCathepsin KNfatc1 protein, mouseNFATC Transcription FactorsRANK LigandTartrate-Resistant Acid PhosphataseTNFSF11 protein, humanbone resorptiondifferentiationNFATc1OsteoclastosteoclastogenesisRAW264.7tartrate-resistant acid phosphatase

Identifiers

PMID31947698
PMCPMC7013577
OpenAlexW2998740880

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.