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


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
31 May 2021
Historique:
received: 30 04 2021
revised: 20 05 2021
accepted: 26 05 2021
entrez: 2 6 2021
pubmed: 3 6 2021
medline: 8 7 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 34073015
pii: ijms22115944
doi: 10.3390/ijms22115944
pmc: PMC8198053
pii:
doi:

Substances chimiques

Serum Amyloid P-Component 0
PTX3 protein 148591-49-5
C-Reactive Protein 9007-41-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : This research was funded by BRIC-INAIL (2019#23)
ID : (2019#23)

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Chiara Greggi (C)

Medical-Surgical Biotechnologies and Translational Medicine, "Tor Vergata" University of Rome, via Montpellier 1, 00133 Rome, Italy.
Department of Clinical Sciences and Translational Medicine, "Tor Vergata" University of Rome, via Montpellier 1, 00133 Rome, Italy.

Ida Cariati (I)

Medical-Surgical Biotechnologies and Translational Medicine, "Tor Vergata" University of Rome, via Montpellier 1, 00133 Rome, Italy.
Department of Clinical Sciences and Translational Medicine, "Tor Vergata" University of Rome, via Montpellier 1, 00133 Rome, Italy.

Federica Onorato (F)

Department of Orthopaedics and Traumatology, "Policlinico Tor Vergata" Foundation, viale Oxford 81, 00133 Rome, Italy.

Riccardo Iundusi (R)

Department of Orthopaedics and Traumatology, "Policlinico Tor Vergata" Foundation, viale Oxford 81, 00133 Rome, Italy.

Manuel Scimeca (M)

Department of Biomedicine and Prevention, "Tor Vergata" University of Rome, via Montpellier 1, 00133 Rome, Italy.

Umberto Tarantino (U)

Department of Clinical Sciences and Translational Medicine, "Tor Vergata" University of Rome, via Montpellier 1, 00133 Rome, Italy.
Department of Orthopaedics and Traumatology, "Policlinico Tor Vergata" Foundation, viale Oxford 81, 00133 Rome, Italy.

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