The stabilisation of collagen fibres during development and through growth
to maturation is now fairly well understood. It is a carefully controlled e
nzymic process which produces intermolecular cross-links at specific locati
ons. In marked contrast, the changes in the physical properties that occur
towards old age are stochastic and involve oxidative reactions that result
in the formation of glucose mediated cross-links, This excessive and random
cross-linking leads to a devastating loss of tissue functionality and dete
rioration of vital organs. In addition, specific residues involved in cell-
matrix interactions may become modified. This can affect the expression of
cells and lead to the formation of an inappropriate collagen matrix during
its slower turnover in old age. This is exemplified in the ubiquitous disor
ders osteoporosis and osteoarthritis, age-related diseases in which we have
noted gene regulated changes in the collagen deposited and also post-trans
lational changes such as over-hydroxylation of lysine residues. Both of the
se effects can have a profound deleterious effect on the function of the ma
trix tissue.