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1.
Tissue Eng Part A ; 16(5): 1575-84, 2010 May.
Article in English | MEDLINE | ID: mdl-19938962

ABSTRACT

Tissue-engineered cartilage may be expected to serve as an alternative to autologous chondrocyte transplantation treatment. Several methods for producing cartilaginous tissue have been reported. In this study, we describe the production of scaffold-free stiff cartilaginous tissue of pig and human, using allogeneic serum and growth factors. The tissue was formed in a mold using chondrocytes recovered from alginate bead culture and maintained in a medium with transforming growth factor-beta and several other additives. In the case of porcine tissue, the tear strength of the tissue and the contents of proteoglycan (PG) and collagen per unit of DNA increased dose-dependently with transforming growth factor-beta. The length of culture was significantly and positively correlated with thickness, tear strength, and PG and collagen contents. Tear strength showed positive high correlations with both PG and collagen contents. A positive correlation was also seen between PG content and collagen content. Similar results were obtained with human cartilaginous tissue formed from chondrocytes expanded in monolayer culture. Further, an in vivo pilot study using pig articular cartilage defect model demonstrated that the cartilaginous tissue was well integrated with surrounding tissue at 13 weeks after the implantation. In conclusion, we successfully produced implantable scaffold-free stiff cartilaginous tissue, which characterized high PG and collagen contents.


Subject(s)
Cartilage/physiology , Collagen/metabolism , Intercellular Signaling Peptides and Proteins/pharmacology , Proteoglycans/biosynthesis , Tissue Culture Techniques/methods , Tissue Engineering/methods , Tissue Scaffolds/chemistry , Aged , Aged, 80 and over , Animals , Cartilage/drug effects , Female , Humans , Materials Testing , Mechanical Phenomena/drug effects , Middle Aged , Models, Animal , Sus scrofa
2.
J Vet Med Sci ; 69(9): 915-24, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17917376

ABSTRACT

In this study, a retrospective analysis was conducted to assess the current aspects and predisposing factors of canine sterile panniculitis. Miniature dachshund, neutered, and younger dogs appeared to be predisposed. In addition, histories of previous surgery and injection were associated in 46.5% of the cases, with several types of surgical suture materials used. About 88% of the dogs had multifocal lesions, frequently with signs of systemic illnesses. Whereas systemic immunosuppressive therapy was effective in most dogs, surgical excision of lesions was rarely curative. In order to prevent recurrences, over 65% of the cases required prolonged immunosuppressive therapy. Polymorphism of canine alpha(1)AT gene was investigated as a candidate gene for sterile panniculitis. Eight polymorphisms were discovered in seven Miniature dachshunds by direct nucleotide sequencing, which included a 12-bp deletion, three non-synonymous single nucleotide polymorphisms, and four silent substitutions. Genotyping of the two polymorphisms, c.109_120del12 and c.483A>C, which identified at high incidence in the dachshunds, was conducted in 83 dogs of 6 popular breeds. The frequencies of neither polymorphism differed between Miniature dachshunds and other breeds, suggesting that neither is responsible for developing panniculitis.


Subject(s)
Dog Diseases/etiology , Panniculitis/etiology , alpha 1-Antitrypsin/genetics , Alleles , Animals , Base Sequence , Cloning, Molecular , Dog Diseases/genetics , Dogs , Female , Genetic Predisposition to Disease , Genotype , Male , Molecular Sequence Data , Panniculitis/genetics , Polymorphism, Single Nucleotide , Retrospective Studies , Reverse Transcriptase Polymerase Chain Reaction/veterinary , Sequence Homology
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