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Originally published as JHC exPRESS on July 24, 2006.
doi:10.1369/jhc.6A6959.2006
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Journal of Histochemistry and Cytochemistry
Volume 54 (11): 1215-1228, 2006
Copyright ©The Histochemical Society, Inc.

Three-dimensional Reconstruction of Fracture Callus Morphogenesis

Louis C. Gerstenfeld, Yaser M. Alkhiary, Elizabeth A. Krall, Fred H. Nicholls, Stephanie N. Stapleton, Jennifer L. Fitch, Megan Bauer, Rayyan Kayal, Dana T. Graves, Karl J. Jepsen and Thomas A. Einhorn

Orthopaedic Research Laboratory, Boston University Medical Center, Boston, Massachusetts (LCG,FHN,SNS,JLF,TAE); Prosthodontics Division, Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia (YMA); Department of Health Policy and Health Services Research (EAK) and Department of Periodontology and Oral Biology (MB,RK,DTG), Boston University School of Dental Medicine, Boston, Massachusetts; and Department of Orthopaedics, Mount Sinai School of Medicine, New York, New York (KJJ)

Correspondence to: Louis C. Gerstenfeld, PhD, Orthopaedic Research Laboratory, Boston University Medical Center, 715 Albany Street, R-205, Boston, MA 02118. E-mail: lgersten{at}bu.edu

Rat and mouse femur and tibia fracture calluses were collected over various time increments of healing. Serial sections were produced at spatial segments across the fracture callus. Standard histological methods and in situ hybridization to col1a1 and col2a1 mRNAs were used to define areas of cartilage and bone formation as well as tissue areas undergoing remodeling. Computer-assisted reconstructions of histological sections were used to generate three-dimensional images of the spatial morphogenesis of the fracture calluses. Endochondral bone formation occurred in an asymmetrical manner in both the femur and tibia, with cartilage tissues seen primarily proximal or distal to the fractures in the respective calluses of these bones. Remodeling of the calcified cartilage proceeded from the edges of the callus inward toward the fracture producing an inner-supporting trabecular structure over which a thin outer cortical shell forms. These data suggest that the specific developmental mechanisms that control the asymmetrical pattern of endochondral bone formation in fracture healing recapitulated the original asymmetry of development of a given bone because femur and tibia grow predominantly from their respective distal and proximal physis. These data further show that remodeling of the calcified cartilage produces a trabecular bone structure unique to fracture healing that provides the rapid regain in weight-bearing capacity to the injured bone. (J Histochem Cytochem 54:1215–1228, 2006)

Key Words: fracture repair • bone histomorphometry • growth and development • three-dimensional reconstructions • orthopedics


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