Related Experiment Video
Updated: May 8, 2026

11:22
Treatment of Osteochondral Defects in the Rabbit's Knee Joint by Implantation of Allogeneic Mesenchymal Stem Cells in Fibrin Clots
Published on: May 21, 2013
Synoviocyte neotissues towards in vitro meniscal tissue engineering
Jennifer J Warnock1, Katja F Duesterdieck-Zellmer, Gerd Bobe
1Oregon State University, College of Veterinary Medicine, 105 Magruder Hall, 700 SW 30th St., Corvallis, OR 97331, United States.
Research in Veterinary Science
|August 28, 2013
Summary
Tensioning synoviocyte neotissues improved cell viability and promoted fibrochondrogenic activity. This method shows promise for in vitro meniscal tissue engineering in dogs with osteoarthritis.
Area of Science:
- Veterinary Medicine
- Biomaterials Science
- Regenerative Medicine
Background:
- Meniscal injuries are a frequent cause of stifle joint pain and osteoarthritis in dogs.
- Current treatments often fail to fully restore joint function, highlighting the need for advanced therapeutic strategies.
Purpose of the Study:
- To investigate the production of synoviocyte-derived autologous neotissues for meniscal tissue engineering in dogs.
- To compare two culture techniques: contracted versus tensioned synthesis of synoviocyte neotissues.
Main Methods:
- Synoviocytes were isolated from 14 client-owned dogs with naturally occurring stifle osteoarthritis during routine arthroscopy.
- Neotissues were cultured using either contracted or tensioned synthesis methods.
- Analyses included meniscal-like matrix components, gene expression (fibrochondrogenesis, inflammation), cell viability, and protein content.
Main Results:
- Tension significantly improved cell viability and enhanced fibrochondrogenic activity.
- Tension upregulated collagen type 1 and aggrecan gene expression while downregulating IL-6.
- Tension increased collagen protein content and the chondrogenic index of the neotissues.
Conclusions:
- Applying tension to synoviocytes is a viable method for in vitro meniscal tissue engineering.
- Tensioned synthesis promotes a more favorable cellular environment for neotissue development, potentially aiding in osteoarthritis management.
Keywords:
ASMCSCSNCell cultureDMEMECMGAGGAPDHIHCILMeniscusOsteoarthritisRNART-PCRSEMSOX-9SynoviumTBSTNFαTSNTissue engineeringalpha smooth muscle actincell sheetscontracted synoviocyte neotissueextracellular matrixglyceraldehyde 3-phosphate dehydrogenaseglycosaminoglycanshigh glucose Dulbecco’s modified Eagle’s mediaimmunohistochemistryinterleukinreal-time reverse-transcriptase polymerase chain reactionribonucleic acidsry-type homeobox protein-9standard error of the meantensioned synoviocyte neotissuetris buffered salinetumor necrosis factor-alpha