Author/Authors :
Charles H. Rundle، نويسنده , , Hali Wang، نويسنده , , Hongrun Yu، نويسنده , , Robert B. Chadwick، نويسنده , , Emile I. Davis، نويسنده , , Jon E. Wergedal، نويسنده , , K. -H. William Lau، نويسنده , , Subburaman Mohan، نويسنده , , James T. Ryaby، نويسنده , , David J. Baylink، نويسنده ,
Abstract :
Microarray analysis of gene expression was performed in the healing femur fractures of 13-week-old male rats during the inflammatory stage
of repair, at 3 days post-fracture, and the endochondral bone formation stage of repair, at 11 days post-fracture. Multiple replicate pairs of fracture
tissues paired with unfractured tissues, and unfractured control bones that had the stabilizing K-wire were introduced. This approach normalized
the marrow contributions to the RNA repertoire. We identified 6555 genes with significant changes in expression in fracture tissues at 3 days and
11 days healing. The repertoire of growth factor genes expressed was also surprisingly restricted at both post-fracture intervals. The large number
of Expressed Sequence Tags (ESTs) expressed at both post-fracture times indicates that several molecular pathways yet to be identified regulate
fracture repair. The number of genes expressed during immune responses and inflammatory processes was restricted with higher expression
largely during the early post-fracture analysis. Several of the genes identified in this study have been associated with regulation of cell and
extracellular matrix interactions during scarless healing of fetal skin wounds. These observations suggest that these genes might also regulate the
scarless healing characteristic of bone regeneration by similar mechanisms.
Keywords :
inflammation , Scarless , Endochondral , Microarray , Fracture Healing