Objective-Thrombospondin-1 (TSP-1), a trimeric glycoprotein, is involved in
cell-matrix interactions of various tissues, particularly in cartilage. Bi
ochemical analyses show expression of TSP-l in human cartilage, but its cel
lular source as web as the presence of its main surface receptors CD36 and
CD51 in normal and osteoarthritic cartilage remain unknown. Therefore, to l
ocalise TSP-1 and its receptors immunohistochemistry and in situ hybridisat
ion were used.
Methods-Radioactive in situ hybridisations with an RNA probe that encodes T
SP-1 combined with immunostaining were carried out to investigate the expre
ssion patterns of TSP-1, CD36, and CD51 in seven normal and 23 osteoarthrit
ic human cartilage samples.
Results-In normal cartilage TSP-1 was present mainly in the middle and uppe
r deep zone. RNA expression was predominantly seen over chondrocytes of the
middle zone. CD36 was found in chondrocytes of the superficial and upper m
iddle zone. In mild and moderate osteoarthritic cartilage an increased numb
er of TSP-1 expressing chondrocytes were seen and an increased pericellular
staining close to the surface. In severe osteoarthritic cartilage a decrea
se in the number of TSP-1 synthesising chondrocytes and a strong reduction
in matrix staining were observed, Most of these severe osteoarthritic sampl
es showed a strongly enhanced number of CD36 positive chondrocytes.
Conclusion-The cellular source of TSP-1 in normal cartilage is mainly mid-z
one chondrocytes, which also express CD36. In early osteoarthritic cartilag
e lesions an increase of TSP-1 uas seen, whereas reduced TSP-1 synthesis is
paralleled by a strong decrease in TSP-1 protein staining in severe osteoa
rthritis. Furthermore, in severe osteoarthritic cartilage the number of CD3
6 immunostained chondrocytes is significantly increased.