We prepared a collagen sponge made of type I and III bovine collagen,
glycosaminoglycans (GAG) and chitosan. Fibroblasts grown within the co
llagen sponge express a sixfold increase of their collagen synthesis,
compared with fibroblasts embedded in a collagen gel. Moreover, collag
en synthesis is twice as high in the collagen sponge than in a monolay
er culture. The collagen sponge culture system promotes a dynamic mode
l for us to perform studies on the regulations of collagen synthesis.
Increased collagen production within the collagen sponge leads fibrobl
asts to reconstitute their own extracellular matrix, which should be m
ore physiological than a bovine collagen gel.