Immunodetection and partial cDNA sequence of the proteoglycan, superficial zone protein, synthesized by cells lining
B L Schumacher1, C E Hughes, K E Kuettner
1Department of Biochemistry, Rush Medical College at Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois 60612, USA. bshumac@rush.edu
Insights
Superficial zone protein, a large proteoglycan, is synthesized by chondrocytes and synovial cells lining the articular cavity. This finding highlights its potential as a marker for these specific joint cells.
Area of Science:
- Biochemistry
- Cell Biology
- Immunology
Background:
- Superficial zone protein (SZP) is a large proteoglycan found in bovine articular cartilage.
- Understanding SZP's cellular origin is crucial for its application as a biomarker.
Purpose of the Study:
- To identify the specific cells within the joint that synthesize superficial zone protein.
- To validate SZP as a phenotypic marker for articular cavity lining cells.
Main Methods:
- Monoclonal antibodies were generated against SZP.
- Western blot analysis and immunohistochemical studies were performed.
- A cDNA fragment encoding part of SZP was isolated from a bovine chondrocyte library.
Main Results:
- SZP was localized predominantly in chondrocytes of the superficial zone of articular cartilage and in synovial lining cells.
- SZP was not detected in deep zone chondrocytes, nasal cartilage, or synovial stromal cells.
- Flow cytometry revealed immunopositivity in 37.4% of full-thickness chondrocytes, 52.5% of superficial zone chondrocytes, and 7.5% of synovial cells.
Conclusions:
- Both articular chondrocytes and synovial cells synthesize superficial zone protein.
- SZP serves as a valuable phenotypic marker for cells lining the articular cavity.
Abstract:
We have previously described a large proteoglycan named superficial zone protein that was isolated and purified from culture medium of superficial slices of bovine articular cartilage. Monoclonal antibodies were raised against superficial zone protein and used as probes in Western blot analyses for immunohistochemical studies both to determine precisely which cells within the joint synthesize the proteoglycan and to isolate a cDNA fragment from a bovine chondrocyte lambdagt11 library that encodes part of the proteoglycan. The cDNA fragment that was obtained with use of monoclonal antibody 6-A-1 encodes the 3' end of the sequence for superficial zone protein. On Western blots, monoclonal antibody 3-A-4 recognized an epitope on native, but not reduced, superficial zone protein, whereas monoclonal antibody 6-A-1 reacted with both native and denatured antigen. The proteoglycan was immunolocalized with monoclonal antibody 3-A-4 in chondrocytes predominantly within the superficial zone of fetal and adult articular cartilage and in some cells of the synovial lining. However, the proteoglycan was not detected in chondrocytes deep in articular cartilage, in nasal septal cartilage, or in synovial stromal cells. The only matrix staining positively for superficial zone protein was at the articular surface bordering the synovial cavity in adult, but not fetal, joints. Isolated chondrocytes and synovial cells showed intracellular binding of monoclonal antibody 3-A-4, and flow-cytometric analysis with the antibody gave the following percentages of immunopositive cells: 37.4, 52.5, 3.4, and 7.5 from chondrocytes from the full-thickness, superficial, and deep zones and from synovial cells, respectively. Thus, both chondrocytes and synovial cells bordering the joint cavity synthesize superficial zone protein and substantiate its usefulness as a phenotypic marker of particular cellular species lining the articular cavity.
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