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Increasing platelet concentration in platelet‐rich plasma inhibits anterior cruciate ligament cell function in three‐dimensional culture
Author(s) -
Yoshida Ryu,
Cheng Mingyu,
Murray Martha M.
Publication year - 2014
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.22493
Subject(s) - platelet rich plasma , apoptosis , platelet , chemistry , anterior cruciate ligament , cell culture , andrology , cell , viability assay , cell growth , tissue engineering , microbiology and biotechnology , immunology , biology , medicine , biomedical engineering , surgery , biochemistry , genetics
Tissue engineering is one new strategy being developed to treat ACL ruptures. One such approach is bio‐enhanced ACL repair, where a suture repair is supplemented with a bio‐active scaffold containing platelets. However, the optimal concentration of platelets to stimulate ACL healing is not known. We hypothesized that increasing platelet concentrations in the scaffold would enhance critical cell behaviors. Porcine ACL fibroblasts were obtained from explant culture and suspended in platelet poor plasma (PPP), 1× platelet‐rich plasma (PRP), 3× PRP, 5× PRP, or phosphate buffered saline (PBS). The cell suspensions were cultured in a 3D collagen scaffold. Cellular metabolism (MTT assay), apoptosis (TUNEL assay), and gene expression for type I and type III collagen were measured. 1× PRP significantly outperformed 5× PRP in all parameters studied: Type I and III collagen gene expression, apoptosis prevention, and cell metabolism stimulation. ACL fibroblasts cultured with 1× PRP had the highest type I and type III collagen gene expression. 1× PRP and PPP groups had the highest cell metabolism and lowest apoptosis rates. Concentration of platelets had significant effects on the behavior of ACL fibroblasts; thus, it is an important parameter that should be specified in clinical or basic science studies. © 2013 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 32:291–295, 2014.