The objectives of this proposal are to determine the mechanisms by which an osteoinductive material, demineralized bone powder (DBP), initiates chondrogenesis in human dermal fibroblasts in vitro, and to determine the fate of induced cartilage when implanted in vivo. The proposed studies will critically test the hypothesis that a change in expression of specific """"""""master"""""""" gene(s) initiates induction of the chondrocyte phenotype in fibroblasts by DBP.
Specific Aim I is to optimize the 3D culture system for maintenance of expression of chondrocyte phenotype. Goldring's immortalized adult human chondrocytes (T/C-28a4) will be used as a positive control for optimizing culture conditions, in order to permit quantitative analysis of chondrocyte markers, including immunohistochemical, biochemical (collagen type II, proteoglycans and GAGs) and molecular ones (COL2A1, aggrecan, link protein). Variables will include extracellular matrix components (chondroitin-sulfate, heparan-sulfate, hyaluronan) and continuous, or intermittent hydrostatic pressure.
Specific Aim II is to characterize, by biochemical and molecular means, chondroinduction in human dermal fibroblasts cultured with DBP. The applicants will examine the sequence in which human dermal fibroblasts, cultured in collagen sponges with DBP, express features of the chondrocyte phenotype that result in cartilage matrix accumulation. Permanence will be determined by assessment of phenotype after cells are separated from DBP. Outcome measures include immunohistochemical characterization of matrix components and quantitative biochemical assessment of production of cartilage-specific collagen and proteoglycans. Expression of cartilage-specific genes will be demonstrated by RT-PCR, Northern hybridization and in situ hybridization.
Specific Aim III is to identify regulatory genes controlling chondroinduction. Using the earliest markers of in vitro chondroinduction, efforts will be made to identify regulatory factor(s) that initiate chondroinduction by DBP. Candidate transcription factors that will be examined include scleraxis, SOX9, HOXC8 and twist. In addition, the applicants propose to use a highly sensitive technique of representational display analysis (RDA), previously used to identify rare transcripts that are up-regulated or repressed. Putative """"""""master"""""""" gene(s) will be expressed for proof of function. Finally, Specific Aim IV is to test the fate of induced chondrocytes in vivo.
|Yates, Karen E; Allemann, Florin; Glowacki, Julie (2005) Phenotypic analysis of bovine chondrocytes cultured in 3D collagen sponges: effect of serum substitutes. Cell Tissue Bank 6:45-54|
|Glowacki, J; Yates, K E; Maclean, R et al. (2005) In vitro engineering of cartilage: effects of serum substitutes, TGF-beta, and IL-1alpha. Orthod Craniofac Res 8:200-8|
|Mizuno, Shuichi; Glowacki, Julie (2005) Low oxygen tension enhances chondroinduction by demineralized bone matrix in human dermal fibroblasts in vitro. Cells Tissues Organs 180:151-8|
|Yates, Karen E (2004) Inferred functions of ""novel"" genes identified in fibroblasts chondroinduced by demineralized bone. DNA Cell Biol 23:15-24|
|Yates, Karen E; Forbes, Rachel L; Glowacki, Julie (2004) New chondrocyte genes discovered by representational difference analysis of chondroinduced human fibroblasts. Cells Tissues Organs 176:41-53|
|Zhou, Shuanhu; Glowacki, Julie; Yates, Karen E (2004) Comparison of TGF-beta/BMP pathways signaled by demineralized bone powder and BMP-2 in human dermal fibroblasts. J Bone Miner Res 19:1732-41|
|Yates, Karen E; Glowacki, Julie (2003) Altered expression of connective tissue genes in postnatal chondroinduced human dermal fibroblasts. Connect Tissue Res 44:121-7|
|Mizuno, Shuichi; Tateishi, Tetsuya; Ushida, Takashi et al. (2002) Hydrostatic fluid pressure enhances matrix synthesis and accumulation by bovine chondrocytes in three-dimensional culture. J Cell Physiol 193:319-27|
|Yates, K E; Mizuno, S; Glowacki, J (2001) Early shifts in gene expression during chondroinduction of human dermal fibroblasts. Exp Cell Res 265:203-11|
|Glowacki, J (2001) Engineered cartilage, bone, joints, and menisci. Potential for temporomandibular joint reconstruction. Cells Tissues Organs 169:302-8|
Showing the most recent 10 out of 11 publications