P. Virolainen et al., EXPRESSION OF MATRIX GENES DURING INCORPORATION OF CANCELLOUS BONE ALLOGRAFTS AND AUTOGRAFTS, Clinical orthopaedics and related research, (317), 1995, pp. 263-272
The healing process of cylindrical metaphyseal bone defects filled wit
h fresh autogeneic or frozen allogeneic cancellous bone grafts was stu
died using histology, biomechanical testing, and molecular biology, Th
e results were compared with the healing pattern observed in nongrafte
d defects, where a strong initial expression of Type III collagen was
followed by slowly starting expression of osteonectin and Type 1 colla
gen genes, Autogeneic or allogeneic cancellous bone grafts considerabl
y increased the healing rate of the defects, The sequence of healing w
as similar with both types of grafts, but the maximal levels of Type I
II and Type I collagen messenger ribonucleic acids (mRNAs) were delaye
d by 1 week when allografts were used, Histologically, during the init
ial phase the grafts had an invasion of progenitor mesenchymal tissue
within 2 weeks followed by intramembranous bone formation and by a gra
dual decline in Type I collagen expression, Osteonectin mRNA was prese
nt throughout the healing process, but no expression of Type II collag
en was seen, Indentation testing showed no significant biomechanical d
ifferences between the autografts and allografts, Histology and molecu
lar biology testing results revealed that the production of extracellu
lar matrix starts slower in allogeneic cancellous bone grafts than in
autografts, suggesting a basic difference in the initial host tissue r
esponse between autogeneic and allogeneic bone grafts.