Immunolocalization of IL-17A, IL-17B, and their receptors in chondrocytes during fracture healing.

Authors:
Takeshi Kokubu
Takeshi Kokubu
Kobe University Graduate School of Medicine
Japan
Prof. Dominik R Haudenschild, Ph.D.
Prof. Dominik R Haudenschild, Ph.D.
University of California Davis Medical Center
Professor
Arthritis Research
Sacramento, CA | United States
Timothy A Moseley
Timothy A Moseley
NuVasive
San Diego | United States

J Histochem Cytochem 2008 Feb 6;56(2):89-95. Epub 2007 Sep 6.

Center for Tissue Regeneration and Repair, Department of Orthopedics, University of California, School of Medicine, 4635 Second Avenue, Sacramento, CA 95817, USA.

Fracture healing in long bones is a sequential multistep cascade of hemostasis, transient inflammation, chemotaxis of progenitor cells, mitosis, differentiation of cartilage, and replacement with bone. This multistep cascade is orchestrated by cytokines and morphogens. Members of the interleukin (IL)-17 family, including IL-17B, have been identified in cartilage, but their expression during fracture healing is unknown. In this study, we determined the immunolocalization of cytokines IL-17A and IL-17B, along with the IL-17 receptor (IL-17R) and IL-17 receptor-like protein (IL-17RL), during the sequence of fracture repair in a standard model. The results were extended to developmental changes in the epiphyseal growth plate of long bones. Members of the IL-17 family were localized in chondrocytes in the fracture callus. Moreover, we found significant parallels to the localization of these cytokines and their receptors in chondrocytes during an endochondral differentiation program in the epiphyseal growth plate.

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http://dx.doi.org/10.1369/jhc.7A7223.2007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2324170PMC

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February 2008
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