Bone marrow stimulation induces greater chondrogenesis in trochlear vs condylar cartilage defects in skeletally mature rabbits

Osteoarthritis Cartilage. 2013 Jul;21(7):999-1007. doi: 10.1016/j.joca.2013.04.010. Epub 2013 Apr 20.

Abstract

Objective: The aim of this study was to compare the early repair response of cartilage defects in trochlea (TR) and medial femoral condyle (MFC) at 2-3 weeks after bone marrow stimulation.

Design: Bilateral full-thickness cartilage defects were generated in central trochlear groove and MFC of skeletally mature rabbits. Four subchondral perforations were made on each defect, either by microfracture to 2 mm deep, or by drilling to 2 mm or 6 mm deep. Rabbits were sacrificed either on Day 14 post-operatively or on Day 21. Defects were analyzed by histology, stereology, histomorphometry and micro-computed tomography (CT). Intact femurs (N = 4) served as controls.

Results: Stromal cell density recruitment was similar in all defects, irrespective of defect location and surgical techniques used. There was a robust appearance of chondrocytes at Day 21 in TR defects with significantly higher volume fraction of chondrocytes in TR compared to MFC (P = 0.013). Chondrogenic foci were observed in marrow penetrating holes, with a significantly higher frequency and larger foci in TR vs MFC defects at Day 21 (P = 0.043 and P = 0.0014, respectively). Micro-CT analysis showed that deep drilling elicited significantly more mineralized bone fill compared to shallower perforations at 2 and 3 weeks repair (all at P ≤ 0.0008).

Conclusions: Bone marrow stimulation induced greater chondrogenesis in TR vs MFC defects in adult rabbits, with more chondrocytes and larger chondrogenic foci appearing in TR vs MFC on Day 21 post-operation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthroplasty, Subchondral / methods
  • Bone Cements / therapeutic use
  • Cartilage Diseases / surgery
  • Cartilage, Articular / diagnostic imaging
  • Cartilage, Articular / physiology*
  • Cartilage, Articular / surgery
  • Case-Control Studies
  • Chondrocytes / diagnostic imaging
  • Chondrocytes / metabolism*
  • Chondrogenesis / physiology*
  • Collagen Type II / metabolism
  • Disease Models, Animal
  • Femur / diagnostic imaging
  • Femur / physiology*
  • Femur / surgery
  • Hindlimb
  • Mesenchymal Stem Cells / diagnostic imaging
  • Mesenchymal Stem Cells / metabolism*
  • Methylmethacrylate / therapeutic use
  • Osteoclasts / metabolism
  • Rabbits
  • Wound Healing / physiology
  • X-Ray Microtomography

Substances

  • Bone Cements
  • Collagen Type II
  • Methylmethacrylate