Cellular basis for age-related changes in fracture repair

Chuanyong Lu, Theodore Miclau, Diane Hu, Erik Hansen, Kathy Tsui, Christian Puttlitz, Ralph S. Marcucio

Research output: Contribution to journalArticle

138 Scopus citations

Abstract

The goal of this work was to define cellular and molecular changes that occur during fracture healing as animals age. We compared the molecular, cellular, and histological progression of skeletal repair in juvenile (4 weeks old), middle-aged (6 months old), and elderly (18 months old) mice at 3, 5, 7, 10, 14, 21, 28, and 35 days post-fracture, using a non-stabilized tibia fracture model. Our histological and molecular analyses demonstrated that there was a sharp decline in fracture healing potential between juvenile and middle-aged animals, while a more subtle decrease in healing potential was apparent between middle-aged and elderly mice. By three days after fracture, chondrocytes expressing Collagen type II, and osteoblasts expressing osteocalcin, were present in calluses of juvenile, but not middle-aged or elderly, mice. At day 5 immature chondrocytes and osteoblasts were observed in calluses of middle-aged and elderly mice. While at this time, chondrocytes in juvenile mice were expressing Collagen type X(ColX) indicating that chondrocyte maturation was already underway. At day 7, chondrocytes expressing ColX were abundant in middle-aged mice while a small domain of ColX-positive chondrocytes were observed in elderly mice. Further, in juvenile and middle-aged mice, but not elderly mice, vascular invasion of the cartilage was underway by day 7. Juvenile mice had replaced nearly all of the cartilage by day 14, while cartilage was still present in the callus of middle-aged mice at day 21 and in elderly mice at day 28. In addition to these delays, histomorphometry revealed that elderly and middle-aged mice formed less bone than juveniles (p < 0.001), while cartilage production was unaffected (p > 0.22). Collectively, these data suggest that enhancing cell differentiation, improving osteoblast function, and accelerating endochondral ossification may significantly benefit the elderly.

Original languageEnglish (US)
Pages (from-to)1300-1307
Number of pages8
JournalJournal of Orthopaedic Research
Volume23
Issue number6
DOIs
StatePublished - Nov 2005
Externally publishedYes

Keywords

  • Aging
  • Chondrocyte
  • Fracture repair
  • Osteoblasts
  • Remodeling

ASJC Scopus subject areas

  • Orthopedics and Sports Medicine

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  • Cite this

    Lu, C., Miclau, T., Hu, D., Hansen, E., Tsui, K., Puttlitz, C., & Marcucio, R. S. (2005). Cellular basis for age-related changes in fracture repair. Journal of Orthopaedic Research, 23(6), 1300-1307. https://doi.org/10.1016/j.orthres.2005.04.003