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This research explores the engineering of temporomandibular joint (TMJ) discs, focusing on the challenges of recreating their complex structure to address disorders affecting millions, particularly young females. Our approach involves using electrospun scaffolds and culturing bovine fibrochondrocytes in various gel environments to assess their growth and extracellular matrix production. Initial findings indicate that cells thrive better in collagen gels than in agarose, suggesting a pathway to improve TMJ disc repair strategies. Future work will include testing growth factors to enhance matrix protein production.
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Engineering a TMJ Disc Danielle Lewis Louisiana Tech University REU, University of Louisiana at Lafayette Dr. David Mills Louisiana Tech University
What is a TMJ Disc? • Temporomandibular Joint Disc • Located between the base of the skull and the lower jaw • Allows for smooth opening and closing of the jaw
TMDs: Temporomandibular Disorders • Improper disc placement hampers proper jaw movement, called disc displacements • 7-28% of adult population affected, mainly females between 18 and 25 • No known treatment for disorder • In severe cases discs are completely removed and patients can no longer move jaw
Current Obstacles in Engineering a TMJ disc • Recreating the intricate cellular structure • 3 regions: anterior band, intermediate zone, and posterior band • Anterior and posterior bands: interlaced collagen fiber bundles • Intermediate zone: aligned collagen fibers along with tiny fibrochondrocytes and small elastin fibers
Approach of the Mills Lab:Electrospun Scaffolds • Electrospinning: • A high voltage is passed through a polymer solution inducing an electrostatic repulsion force • The polymer is pumped through an insulin syringe, the repulsion force results in the formation of a thin jet • This jet is directed toward a grounded collection plate, the solvent evaporates before hitting the collection plate and results in the formation of a polymer scaffold
My Research Plan • Culture bovine fibrochondrocytes (FBCs) in 3 different gel environments – agarose, collagen, alginate • Treat cells with growth factors to observe their effect on proliferation, cell survival and protein expression • bFGF • TGF alpha and beta • CTGF • Characterize the extracellular matrix being produced by the FBCs
Cell Isolations • Bovine FBCs were isolated from TMJ discs taken from cow skulls • Cells used in experiments were passage 6, slightly old but still exhibited the characteristic FBC shape
Gels:Collagen and Agarose • FBCs were suspended in both collagen and agarose gels and allowed to grow for several days, 18 day group and 8 day group
Fixing, Dehydration, and Paraffin Imbedding • Gels fixed in 2% paraformaldehyde • Gels were dehydrated by exposing them to a variety of ethanol solutions then infiltrated with pariffin to preserve them indefinitely • Gels were then imbedded in a paraffin block in preparation for creating slides • Next… Immunohistochemistry
Results • Simple examination under phase contrast showed that FBCs thrived better in collagen gels, cells attached and displayed characteristic shape
Is there any explanation for this observation? • Expected result • Collagen type I abundant in TMJ disc
Conclusions • Bovine fibrochondrocytes appeared to prefer the collagen gel environment over the agarose gel environment
Next Steps…. • Begin staining gels for extra-cellular matrix proteins • Hypothesis: FBCs grown in collagen gels will exhibit an increase in extra-cellular matrix proteins over those grown in agarose gels • Use this experiment as a control and continue by adding growth factors to FBCs in gel culture • Compare the amounts and types of extra-cellular matrix proteins found in gels, both with growth factors and without, to that found in actual disc and FBCs grown on electrospun scaffolds
Thank you… • Dr. Mills, Kanthi, Skylar, Deepak, Stephanie, Paul • Dr. Jones • Louisiana Tech for lab facilities in Carson Taylor and the BME building • National Science Foundation