T. Aigner et al., VARIATION WITH AGE IN THE PATTERN OF TYPE-X COLLAGEN EXPRESSION IN NORMAL AND SCOLIOTIC HUMAN INTERVERTEBRAL DISCS, Calcified tissue international, 63(3), 1998, pp. 263-268
The distribution and expression of type X collagen, a calcium-binding
collagen, which is a marker of hypertrophic chondrocytes and thought t
o be involved in cartilage calcification, was examined in situ in nond
egenerate (grade I or II) human discs taken at autopsy over a wide age
range (fetal->80 years) and also in scoliotic discs removed at surger
y. In the fetal vertebral column, type X collagen was strongly express
ed in the hypertrophic chondrocytes of the endplate, but was not seen
in other areas. In the cartilaginous endplate of adults, it was found
over the whole age range examined, with intensity increasing with age.
In the disc matrix itself, type X collagen was demonstrated around in
dividual cells from all individuals older than 50 years, but not in an
y fetal or autopsy disc from individuals younger than 40 years. In sco
liotic discs, however, focal type X collagen expression was seen in 3/
8 patients younger than 40 years including one 12-year-old. No type X
collagen was found in the outer annulus in any autopsy or scoliotic di
sc, supporting the idea that cells of the outer annulus are phenotypic
ally distinct from cells of the inner annulus and the nucleus. Our res
ults demonstrate for the first time that type X collagen is a possible
gene product of the intervertebral disc cells and a potential biochem
ical component of the disc matrix. They indicate that with age or in s
coliosis, some cells from the inner annulus or nucleus of the disc dif
ferentiate to the hypertrophic chondrocyte phenotype. This might be th
e initiating event for the abnormal calcification described in aged an
d scoliotic discs in other studies.