Jr. Connor et al., Human cartilage glycoprotein 39 (HC gp-39) mRNA expression in adult and fetal chondrocytes, osteoblasts and osteocytes by in-situ hybridization, OSTEO CART, 8(2), 2000, pp. 87-95
Objective: To examine the expression pattern of human cartilage glycoprotei
n 39 (HC gp-39) mRNA in human cartilage and bone.
Design: In-situ hybridization analysis was used to examine the expression p
attern of human cartilage glycoprotein 39 (HC gp-39) mRNA in adult human os
teoarthritic articular cartilage from various stages of disease, as well as
in human osteophytic tissue and in human fetal bone.
Results: In cartilage from patients with mild osteoarthritic cartilage dege
neration, HG gp-39 was expressed at moderate to high levels only in chondro
cytes of the superficial zone. In advanced OA cartilage, cloning chondrocyt
es of the superficial zone expressed high levels of HC gp-39 and chondrocyt
es of the mid- and deep zones were also positive. HC gp-39 was undetectable
in the chondrocytes of normal articular cartilage. In osteophytic tissue,
the expression of HC gp-39 mRNA was intense in flattened, end-stage osteobl
asts and in primary osteocytes in both endochondral and intramembranous bon
e formation. Proliferating osteoblasts expressed low to moderate levels. No
tably, mature osteocytes were negative for HC gp-39 expression. Chondrocyte
s in the secondary ossification center of developing fetal cartilage demons
trated high expression while growth plate and mineralized cartilage chondro
cytes had lower expression. Osteoblasts at sites of endochondral and intram
embranous bone formation were positive for expression of HC gp-39.
Conclusions: The stage-specific expression of HC gp-39 in fetal development
and adult remodelling bone and cartilage provides evidence for a specific
functional or structural role for HC gp-39 in bone and cartilage tissue. HC
gp-39 is expressed in diseased human osteoarthritic cartilage and osteophy
te, but not in non-diseased tissue, and its distribution within the tissue
changes as disease progresses. OA is characterized not only by cartilage de
generation, but by increased subchondral bone formation and osteophytosis.
The results from this study indicate that the increased HC gp-39 expression
in OA serum and synovial fluid may reflect not only cartilage degeneration
but increased osteogenesis. (C) 2000 OsteoArthritis Research Society Inter
national.