Evidence map›Paper›PMID 34073015›Full record

ArticleInternational journal of molecular sciences2021

PTX3 Effects on Osteogenic Differentiation in Osteoporosis: An In Vitro Study.

Chiara Greggi, Ida Cariati, Federica Onorato, Riccardo Iundusi, Manuel Scimeca, Umberto Tarantino

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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
0.9field-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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. [Knockdown ofBeijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
    Article
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  8. Osteoclastogenesis and Osteogenesis.International journal of molecular sciences · 2022
    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

6 authors at 2 institutions in 1 country.

Chiara GreggiMedical-Surgical Biotechnologies and Translational Medicine, "Tor Vergata" University of Rome, via Montpellier 1, 00133 Rome, Italy.ORCID 0000-0003-3205-4030
Ida CariatiMedical-Surgical Biotechnologies and Translational Medicine, "Tor Vergata" University of Rome, via Montpellier 1, 00133 Rome, Italy.ORCID 0000-0002-2102-5034
Federica OnoratoDepartment of Orthopaedics and Traumatology, "Policlinico Tor Vergata" Foundation, viale Oxford 81, 00133 Rome, Italy.
Riccardo IundusiDepartment of Orthopaedics and Traumatology, "Policlinico Tor Vergata" Foundation, viale Oxford 81, 00133 Rome, Italy.
Manuel ScimecaDepartment of Biomedicine and Prevention, "Tor Vergata" University of Rome, via Montpellier 1, 00133 Rome, Italy.ORCID 0000-0003-0585-1309
Umberto TarantinoDepartment of Clinical Sciences and Translational Medicine, "Tor Vergata" University of Rome, via Montpellier 1, 00133 Rome, Italy.
University of Rome Tor Vergata · ITPoliclinico Tor Vergata · IT

Funding

This research was funded by BRIC-INAIL (2019#23) (2019#23)
6 · The paper itself

Abstract

Pentraxin 3 (PTX3) is a glycoprotein belonging to the humoral arm of innate immunity that participates in the body's defence mechanisms against infectious diseases. It has recently been defined as a multifunctional protein, given its involvement in numerous physiological and pathological processes, as well as in the pathogenesis of age-related diseases such as osteoporosis. Based on this evidence, the aim of our study was to investigate the possible role of PTX3 in both the osteoblastic differentiation and calcification process: to this end, primary osteoblast cultures from control and osteoporotic patients were incubated with human recombinant PTX3 (hrPTX3) for 72 h. Standard osteinduction treatment, consisting of β-glycerophosphate, dexamethasone and ascorbic acid, was used as control. Our results showed that treatment with hrPTX3, as well as with the osteogenic cocktail, induced cell differentiation towards the osteoblastic lineage. We also observed that the treatment not only promoted an increase in cell proliferation, but also the formation of calcification-like structures, especially in primary cultures from osteoporotic patients. In conclusion, the results reported here suggest the involvement of PTX3 in osteogenic differentiation, highlighting its osteoinductive capacity, like the standard osteoinduction treatment. Therefore, this study opens new and exciting perspectives about the possible role of PTX3 as biomarker and therapeutic agent for osteoporosis.

Indexed as

OsteoblastsOsteogenesisCalcification, PhysiologicCell DifferentiationCell ProliferationCells, CulturedC-Reactive ProteinHumansMiddle AgedOsteoporosisPentraxinsPrimary Cell CultureSerum Amyloid P-ComponentC-Reactive ProteinPentraxinsSerum Amyloid P-Componentcalcificationmineralizationosteoblastsosteogenic differentiationosteoporosisPTX3

Identifiers

PMID34073015
PMCPMC8198053
OpenAlexW3165678788

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.