Bunion formation in adults is an example of bone growth that occurs after p
hysis closure. Bone is laid down secondary to mechanical irritation caused
by foot deformity. It is a mechanism of ectopic bone formation unrelated to
physeal growth. In this article, bone formation is analyzed using immunohi
stochemical and cell culture techniques. Using markers specific for mesench
ymal cells (collagen type IIa and fibroblast growth factor receptor 3), a c
ell population is defined in the soft tissues that overlie the bunion and i
s isolated from explant cultures. The cells do not produce bone matrix in c
ulture, and they do not express osteoblast-related antigens. Stimulation of
the cells by fibroblast growth factor (FGF) 2 leads to rapid cell prolifer
ation and phenotype change. The cells start to form humps and at the same t
ime express alkaline phosphatase and collagen type I. Expression of collage
n type IIa and fibroblast growth factor receptor 3 ceases. These series of
experiments indicate that a specific population of mesenchymal cells occurs
in the soft tissues that overlie the bunion. This population is capable of
bone formation when stimulated by FGF, a common mediator of inflammatory p
rocesses. Thus, FGF stimulation of mesenchymal cells in soft tissues that o
verlie the head of the first metatarsal is a potential link between the bio
mechanical forces that cause hallux valgus and bunion formation.