Growth factor regulation of fracture repair

GL Barnes, PJ Kostenuik… - Journal of bone and …, 1999 - academic.oup.com
GL Barnes, PJ Kostenuik, LC Gerstenfeld, TA Einhorn
Journal of bone and mineral research, 1999academic.oup.com
FRACTURE REPAIR CAN BE considered as a biologically optimal process resulting in the
restoration of injured skeletal tissue to a state of normal structure and function. Although the
process leads to healing in the vast majority of cases, a small but significant proportion of
fractures result in delayed union or persistent nonunion. Surgical interventions have been
directed toward enhancing the fracture repair process, normalizing the rate of healing, and
decreasing the likelihood of nonunion. During fracture repair, a number of growth factors …
FRACTURE REPAIR CAN BE considered as a biologically optimal process resulting in the restoration of injured skeletal tissue to a state of normal structure and function. Although the process leads to healing in the vast majority of cases, a small but significant proportion of fractures result in delayed union or persistent nonunion. Surgical interventions have been directed toward enhancing the fracture repair process, normalizing the rate of healing, and decreasing the likelihood of nonunion. During fracture repair, a number of growth factors, cytokines, and their cognate receptors are present at elevated levels in and around the fracture site. Many of these proteins are normally expressed in skeletal tissue, and others are released from associated inflammatory cells at the site of injury. The induction of these proteins is regulated both spatially and temporally, suggesting that they play an active role in promoting fracture repair. The following review will summarize the current literature on the roles of the major cytokines and growth factors involved in fracture repair. In addition, the signaling cascades induced by these molecules will be discussed. While many cytokine and growth factor signaling events have not been specifically examined in the context of fracture repair, a large body of literature on signal transduction has emanated from studies on these molecules in embryonic bone development. Given the conserved nature of these molecules and their signaling cascades from Drosophila to humans, and the similarities between the fracture repair process and embryonic bone development, it seems highly probable that these downstream signaling events are conserved in fracture repair.
Fracture repair can be envisioned as involving five distinguishable processes, including the immediate response to injury, intramembranous bone formation, chondrogenesis, endochondral bone formation leading to the reestablishment of load bearing function, and bone remodeling. While these processes may be discussed individually, it should be recognized that the first four occur simultaneously during
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