Re. Topping et al., TYPE-X COLLAGEN IN FRACTURE CALLUS AND THE EFFECTS OF EXPERIMENTAL DIABETES, Clinical orthopaedics and related research, (308), 1994, pp. 220-228
Studies of fracture repair in diabetes have shown decreased mechanical
strength and total collagen in the callus. Type I and Type II collage
n are synthesized by bone and cartilage cells, respectively, while Typ
e X collagen is synthesized by hypertrophic chondrocytes in endochondr
al ossification. A standardized fracture model was chosen to investiga
te extracellular matrix changes during fracture healing of normal and
diabetic rats. Histological examination of the fracture callus in both
normal and diabetic animals showed progression from a fibrous tissue
to cartilage to bone. An antiserum to Type X collagen was prepared, an
d immunostaining was observed in the matrix surrounding the hypertroph
ic chondrocytes. Fracture calluses from streptozotocin induced diabeti
c rats had similar histology and immunostaining to controls. Radiolabe
lled proteins were extracted from the calluses of normal and diabetic
rats to measure Type X collagen. Type X collagen expression in the fra
cture callus of normal rats reached a maximum at day fourteen and was
decreased by between 54% and 70% in the fracture callus of diabetic ra
ts. The decrease in Type X collagen synthesis may have a role in the d
efect of fracture healing in diabetes.