Platelet-rich plasma loaded in situ-formed hydrogel enhances hyaline cartilage regeneration by CB1 upregulation

The efficacy of three‐dimensional (3D) culture on the proliferation and maturation of chondrocytes seeded into a hydrogel scaffold was assessed. Three types of hydrogel were prepared for the 3D culture of primary isolated chondrocytes. Chondrocyte proliferation was assessed using a live/dead viabili...

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Veröffentlicht in:Journal of biomedical materials research. Part A 2012-11, Vol.100A (11), p.3099-3107
Hauptverfasser: Lee, Hye-Rim, Park, Kyung Min, Joung, Yoon Ki, Park, Ki Dong, Do, Sun Hee
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Sprache:eng
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Zusammenfassung:The efficacy of three‐dimensional (3D) culture on the proliferation and maturation of chondrocytes seeded into a hydrogel scaffold was assessed. Three types of hydrogel were prepared for the 3D culture of primary isolated chondrocytes. Chondrocyte proliferation was assessed using a live/dead viability/cytotoxicity assay and semiquantitative RT‐PCR after 3D culture in hydrogel. Cylindrical defects in the center of rat xyphoids were used for the implantation of platelet‐rich plasma (PRP)/hydrogel composites. Rats were killed at day 7 postoperatively and evaluated histochemically and immunohistologically. Xyphoid chondrocytes proliferated well with time in hydrogels. In the PRP‐containing hydrogels, xyphoid defects displayed early formation of chondroid matrix with massive peripheral infiltration of spindle cells. These results were consistent with Safranin‐O staining for proteoglycans and immunohistochemistry for type II collagen. Gene expression analyses in vitro revealed aggrecan, type II collagen, and ChM‐1 and CB1 upregulation by PRP/hydrogel. PRP/hydrogel provided a suitable environment for hyaline cartilaginous regeneration, leading to anti‐inflammation by significant increase of CB1 and inhibiting vascular ingrowth via considerable upregulation of ChM‐1. The results provide a valuable reference for the clinical application of hydrogel scaffolds for hyaline cartilage regeneration, as well as the use of autologous PRP to improve cellular proliferation and maturation of xyphoid repair. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 100A:3099–3107, 2012.
ISSN:1549-3296
1552-4965
DOI:10.1002/jbm.a.34254