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Platelet‐rich plasma impairs osteoclast generation from human precursors of peripheral blood
Author(s) -
Cenni Elisabetta,
Avnet Sofia,
Fotia Caterina,
Salerno Manuela,
Baldini Nicola
Publication year - 2010
Publication title -
journal of orthopaedic research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1002/jor.21073
Subject(s) - rankl , osteoclast , platelet rich plasma , multinucleate , chemistry , acid phosphatase , platelet , microbiology and biotechnology , medicine , endocrinology , receptor , activator (genetics) , biochemistry , biology , enzyme
Platelet‐rich plasma is used to accelerate bone repair for the release of osteogenic growth factors from activated platelets. To date, the effects on osteoclasts have been only scarcely investigated, even though these cells are crucial for bone remodeling. The aim of this research was the evaluation of the effects of thrombin‐activated platelets (PRP) on osteoclastogenesis from human blood precursors. We evaluated both the ability to influence osteoclast differentiation induced by the receptor activator of nuclear factor‐kappaB ligand (RANKL), and the ability to induce osteoclast differentiation without RANKL. In both assays, the incubation with PRP supernatant at 10% did not significantly affect the formation of tartrate‐resistant acid phosphatase (TRACP)‐positive multinucleated cells that were able to form the F‐actin ring. However, when PRP at 25 and 50% was added to the medium without RANKL, the generation of TRACP‐positive multinucleated cells was inhibited. PRP, even at 10%, reduced the osteoclast‐mediated bone collagen degradation, suggesting inhibition of osteoclast activation. Similarly, after incubation with PRP supernatant, calcitonin receptor mRNA was lower than the untreated samples. In conclusion, PRP at 10% interfered with the complete differentiation process of human osteoclast precursors. At higher concentration it impaired osteoclast formation also at an early stage of differentiation. © 2010 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 28:792–797, 2010