Evidence map›Paper›PMID 31752206›Full record

ArticleInternational journal of molecular sciences2019

Calcium Polyphosphate Nanoparticles Act as an Effective Inorganic Phosphate Source during Osteogenic Differentiation of Human Mesenchymal Stem Cells.

Luan Phelipe Hatt, Keith Thompson, Werner E G Müller, Martin James Stoddart, Angela Rita Armiento

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. 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
1.2field-weighted citation impact, top 18% 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, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Micro-porous PLGA/Regenerative biomaterials · 2023
    Article
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  5. Article
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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.

Luan Phelipe HattAO Research Institute Davos, 7270 Davos Platz, Switzerland.ORCID 0000-0001-5278-2209
Keith ThompsonAO Research Institute Davos, 7270 Davos Platz, Switzerland.ORCID 0000-0002-9167-5147
Werner E G MüllerInstitute for Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.ORCID 0000-0002-8223-3689
Martin James StoddartAO Research Institute Davos, 7270 Davos Platz, Switzerland.ORCID 0000-0002-9538-1517
Angela Rita ArmientoAO Research Institute Davos, 7270 Davos Platz, Switzerland.ORCID 0000-0002-3285-0419
AO Foundation · CHJohannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability of bone-marrow-derived mesenchymal stem/stromal cells (BM-MSCs) to differentiate into osteoblasts makes them the ideal candidate for cell-based therapies targeting bone-diseases. Polyphosphate (polyP) is increasingly being studied as a potential inorganic source of phosphate for extracellular matrix mineralisation. The aim of this study is to investigate whether polyP can effectively be used as a phosphate source during the in vitro osteogenic differentiation of human BM-MSCs. Human BM-MSCs are cultivated under osteogenic conditions for 28 days with phosphate provided in the form of organic β-glycerolphosphate (BGP) or calcium-polyP nanoparticles (polyP-NP). Mineralisation is demonstrated using Alizarin red staining, cellular ATP content, and free phosphate levels are measured in both the cells and the medium. The effects of BGP or polyP-NP on alkaline phosphatase (ALP) activity and gene expression of a range of osteogenic-related markers are also assessed. PolyP-NP supplementation displays comparable effects to the classical BGP-containing osteogenic media in terms of mineralisation, ALP activity and expression of osteogenesis-associated genes. This study shows that polyP-NP act as an effective source of phosphate during mineralisation of BM-MSC. These results open new possibilities with BM-MSC-based approaches for bone repair to be achieved through doping of conventional biomaterials with polyP-NP.

Indexed as

Alkaline PhosphataseCalciumCalcium PhosphatesCell Culture TechniquesCell DifferentiationCells, CulturedGene Expression RegulationGlycerophosphatesHumansMesenchymal Stem CellsNanoparticlesOsteogenesisPolyphosphatesAlkaline Phosphatasebeta-glycerophosphoric acidCalciumCalcium PhosphatesGlycerophosphatesPolyphosphatesCa-polyphosphate nanoparticlesinorganic polyphosphatemesenchymal stem cellsosteogenic differentiationβ-glycerolphosphate

Identifiers

PMID31752206
PMCPMC6887735
OpenAlexW2983375739

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.