Abstract

The periosteum is a thin membrane that surrounds the outer surface of bones and participates in fracture healing. However, the molecular signals that trigger/initiate the periosteal reaction are not well established. We fractured the rat femoral bone at the diaphysis and fixed it with an intramedullary inserted wire, and the expression of regenerating gene (Reg) I, which encodes a tissue regeneration/growth factor, was analyzed. Neither bone/marrow nor muscle showed Reg I gene expression before or after the fracture. By contrast, the periosteum showed an elevated expression after the fracture, thereby confirming the localization of Reg I expression exclusively in the periosteum around the fractured areas. Expression of the Reg family increased after the fracture, followed by a decrease to basal levels by six weeks, when the fracture had almost healed. In vitro cultures of periosteal cells showed no Reg I expression, but the addition of IL-6 significantly induced Reg I gene expression. The addition of IL-6 also increased the cell number and reduced pro-apoptotic gene expression of Bim. The increased cell proliferation and reduction in Bim gene expression were abolished by transfection with Reg I siRNA, indicating that these IL-6-dependent effects require the Reg I gene expression. These results indicate the involvement of the IL-6/Reg pathway in the osteogenic response of the periosteum, which leads to fracture repair.

Highlights

  • Bone tissue can be regenerated through osteogenic differentiation of undifferentiated cells into bone-forming osteoblasts

  • We made a fracture at the mid-shaft of a rat femoral bone and stably fixed the fracture site with a wire inserted in the intramedullary region

  • No previous studies have reported regenerating gene (Reg) family expressions in bone tissue regeneration, but the findings presented here clearly show this expression after the fracture (Figures 1f and 2)

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Summary

Introduction

Bone tissue can be regenerated through osteogenic differentiation of undifferentiated cells into bone-forming osteoblasts This regeneration is frequently seen during fracture repair, which produces new bone without scarring. Closer to the fracture site, the tissue damage interrupts the blood supply and leads to the formation of cartilaginous masses both outside and within the cortices. These areas eventually show endochondral bone formation. The periosteum is essential for new bone formation during the fracture repair in the cascades responsible for both endochondral and intramembranous bone formation. Little is known about the nature of the molecules that trigger the periosteal reaction that promotes fracture repair

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