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Revista de Osteoporosis y Metabolismo Mineral
versão On-line ISSN 2173-2345versão impressa ISSN 1889-836X
Resumo
AGUILERA-CORREA, John Jairo et al. The activation of the purinergic system modulates the formation of foreign body giant cells in the presence of different metal alloys for clinical use. Rev Osteoporos Metab Miner [online]. 2024, vol.16, n.4, pp.123-132. Epub 14-Mar-2025. ISSN 2173-2345. https://dx.doi.org/10.20960/revosteoporosmetabminer.00058.
Objective:
two major complications after arthroplasty are prosthetic joint infection, mainly due to Staphylococcus aureus, and the experience of a foreign body reaction by macrophages and foreign body giant cells (FBGCs) regardless of the infection. Our aim is to study the role of purinergic receptors with fusogenic function (P2X7, adenosine A1 and A2A receptors) in the formation of S. aureus-induced FBGCs and their possible differential modulation in the presence of Ti-6Al-4V and Cr-Co-Mo alloys.
Methods:
RAW264.7 cells were differentiated to FBGCs with 20 ng/mL of IL-4 in the presence of adhered unviable S. aureus, metal alloys and/or CGS21680/ZM241385 1 μM. Cell supernatant was collected for nucleotide analysis by HPLC as well as cytokine expression, and cells were lysed for RNA expression.
Results:
the presence of S. aureus induces an increase in FBGCs formation in a concentration-dependent manner. Furthermore, phalloidin staining demonstrated that both Ti-6Al-4V and Cr-Co-Mo alloys reduce the formation of FBGCs. The expression of adenosine A1 and A2A receptors increased after 5 days of differentiation in the presence of S. aureus, and this expression was enhanced with metal alloys. HPLC analyses showed an increase in adenosine in the presence of Ti-6Al-4V and Cr-Co-Mo alloys while ATP was not changed in any of the conditions. The presence of metal alloys induced an increased in IL1β, IL-6 and RANTES.
Conclusions:
the increased levels of adenosine and the adenosine A2A receptor induced by the presence of Ti-6Al-4V and Co-Cr-Mo alloys would be responsible for the inhibition of cell fusion and the following reduction of S. aureus-induced FBGCs.
Palavras-chave : Adenosine; A2A receptor; FBGCs; Metal alloys; Prosthetic joint infection.












