Skip to main content
Log in

Distribution of hyaluronan in articular cartilage as probed by a biotinylated binding region of aggrecan

  • Original Paper
  • Published:
Histochemistry and Cell Biology Aims and scope Submit manuscript

Abstract

The proportion of total tissue hyaluronan involved in interactions with aggrecan and link protein was estimated from extracts of canine knee articular cartilages using a biotinylated hyaluronan binding region-link protein complex (bHABC) of proteoglycan aggregate as a probe in an ELISA-like assay. Microscopic sections were stained with bHABC to reveal free hyaluronan in various sites and zones of the cartilages. Articular cartilage, cut into 20 μm-thick sections, was extracted with 4 M guanidinium chloride (GuCl). Aliquots of the extract (after removing GuCl) were assayed for hyaluronan, before and after papain digestion. The GuCl extraction residues were analyzed after solubilization by papain. It was found that 47–51% of total hyaluronan remained in the GuCl extraction residue, in contrast to the 8–15% of total proteoglycans. Analysis of the extract revealed that 24–50% of its hyaluronan was directly detecable with the probe, while 50–76% became available only after protease digestion. The extracellular matrix in cartilage sections was stained with the bHABC probe only in the superficial zone and the periphery of the articular surfaces, both sites known to have a relatively low proteoglycan concentration. Trypsin pretreatment of the sections enhanced the staining of the intermediate and deep zones, presumably by removing the steric obstruction caused by the chondroitin sulfate binding region of aggrecans. Enhanced matrix staining in these zones was also obtained by a limited digestion with chondroitinase ABC. The results indicate that a part of cartilage hyaluronan is free from endogenous binding proteins, such as aggrecan and link protein, but that the chondroitin sulfate-rich region of aggrecan inhibits its probing in intact tissue sections. Therefore, hyaluronan staining was more intense in cartilage areas with lower aggrecan content. A large proportion of hyaluronan resists GuCl extraction, even from 20-μm-thick tissue sections.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ågren U, Tammi R, Tammi M (1994) A dot blor assay of metabolically radiolabeled hyaluronan. Anal Biochem 217:311–315

    PubMed  Google Scholar 

  • Arokoski J, Kiviranta I, Jurvelin J, Tammi M, Helminen HJ (1993) Long-distance running causes site-dependent decrease of cartilage glycosaminoglycan content in the knee joints of beagle dogs. Arthritis Rheum 36:1451–1459

    PubMed  Google Scholar 

  • Asari A, Miyauchi S, Miyazaki K, Hamai A, Horie K, Takahashi T, Sekiguchi T, Machida A, Kohno K, Uchiyama Y (1992) Intra-and extracellular localization of hyaluronic acid and proteoglycan constituents (chondroitin sulfate, keratan sulfate, and protein core) in articular cartilage of rabbit tibia. J Histochem Cytochem 40:1693–1704

    PubMed  Google Scholar 

  • Asari A, Miyauchi S, Kuriyama S, Machida A, Kohno K, Uchiyama Y (1994) Localization of hyaluronic acid in human articular cartilage. J Histochem Cytochem 42:513–522

    PubMed  Google Scholar 

  • Binderman I, Green RM, Pennypacker JP (1979) Calcification of differentiating skeletal mesenchyme in vitro. Science 206:222–225

    PubMed  Google Scholar 

  • Buckwalter JA, Rosenberg LC, Tang L-H (1984) The effect of link protein on proteoglycan aggregate structure. An electron microscopic study of the molecular architecture and dimensions of proteoglycans reassembled from the proteoglycan monomers and link proteins of bovine fetal epiphyseal cartilage. J Biol Chem 259:5361–5363

    PubMed  Google Scholar 

  • Buckwalter JA, Kuettner KE, Thonar EJ-M (1985) Age-ralted changes in articular cartilage proteoglycans. Electron microscopic studies. J Orthop Res 3:251–257

    PubMed  Google Scholar 

  • Carney SL, Muir H (1988) The structure and function of cartilage proteoglycans. Physiol Rev 68:858–910

    PubMed  Google Scholar 

  • Caterson B, Christner JE, Baker JR, Couchman JR (1985) Production and characterization of monoclonal antibodies directed against connective tissue proteoglycans. Fed Proc 44:386–393

    PubMed  Google Scholar 

  • Craig FM, Bayliss MT, Bentley G, Archer CW (1990) A role for hyaluronan in joint development. J Anat 171:17–23

    PubMed  Google Scholar 

  • Faltz LL, Caputo CB, Kimura JH, Scrode J, Hascall VC (1979) Structure of the complex between hyaluronic acid, the hyaluronic acid binding region, and the link protein of proteoglycan aggregate from the Swarm rat chondrosarcoma. J Biol Chem 254:1381–1387

    PubMed  Google Scholar 

  • Farndale RW, Buttle DJ, Barrett AJ (1986) Improved quantitation and discrimination of sulfated glycosaminoglycans by use of dimethylmethylene blue. Biochim Biophys Acta 883:173–177

    PubMed  Google Scholar 

  • Franzén A, Björnsson S, Heinegård D (1981) Cartilage proteoglycan aggregate formation. Role of link protein. Biochem J 197:669–674

    PubMed  Google Scholar 

  • Hardingham TE, Perkins SJ, Muir H (1983) Molecular conformations of proteoglycan aggregation. Biochem Soc Trans 11: 128–130

    Google Scholar 

  • Hascall VC, Heinegård D (1974) Aggregation of cartilage proteoglycans I. The role of hyaluronic acid. J Biol Chem 249:4232–4241

    PubMed  Google Scholar 

  • Heinegård D, Hascall VC (1974) Aggregation of cartilage proteoglycans. III. Characteristics of the proteins isolated from trypsin digests of aggregates. J Biol Chem 249:4250–4256

    PubMed  Google Scholar 

  • Holmes MWA, Bayliss MT, Muir H (1988) Hyaluronic acid in human articular cartilage. Biochem J 250:435–441

    PubMed  Google Scholar 

  • Homer KA, Denbow L, Beighton D (1993) Spectrophotometric method for the assay of glycosaminoglycans and glycosaminoglycan-depolymerizing enzymes. Anal Biochem 214:435–441

    PubMed  Google Scholar 

  • Iwata M, Wight TN, Carlson SS (1993) A brain extracellular matrix proteoglycan forms aggregates with hyaluronan. J Biol Chem 268:15061–15069

    PubMed  Google Scholar 

  • Kielty CM, Whittaker SP, Grant ME, Shuttleworth CA (1992) Type-VI collagen microfibrils evidence for a structural association with hyaluronan. J Cell Biol 118:979–990

    PubMed  Google Scholar 

  • Kiviranta I, Tammi M, Jurvelin J, Helminen HJ (1987) Topographical variation of proteoglycan content and cartilage thickness in canine (stifle) joint cartilage. Application of the microspectrophotometric method. J Anat 150:265–276

    PubMed  Google Scholar 

  • Knudson CB (1993) Hyaluronan receptor-directed assembly of chondrocyte pericellular matrix. J Cell Biol 120:825–834

    PubMed  Google Scholar 

  • Kongtawelert P, Ghosh P (1990) A method for the quantitation of hyaluronan (hyaluronic acid) in biological fluids using a labeled avidin-biotin technique. Anal Biochem 185:313–318

    PubMed  Google Scholar 

  • Laurent C, Johnson-Wells G, Hellström S, Engström-Laurent A, Wells AF (1991) Localization of hyaluronan in various muscular tissues. A morphological study in the rat. Cell Tissue Res 263:201–205

    PubMed  Google Scholar 

  • LeBaron RG, Zimmermann DR, Ruoslahti E (1992) Hyaluronate binding properties of versican. J Biol Chem 267:10003–10010

    PubMed  Google Scholar 

  • Mason RM, Crossman MV, Sweeney C (1989) Hyaluronan and hyaluronan binding proteins in cartilaginous tissues. In: Evered D, Whelan J (eds) The biology of hyaluronan. Wiley, Chichester, pp 107–120

    Google Scholar 

  • McDevitt CA, Marcelino J, Tucker L (1991) Interaction of intact type-VI collagen with hyaluronan. FEBS Lett 294:167–170

    PubMed  Google Scholar 

  • Morales TI, Hascall VC (1988) Correlated metabolism of proteoglycans and hyaluronic acid in bovine cartilage organ cultures. J Biol Chem 2634:3632–3838

    Google Scholar 

  • Paschalakis P, Vynios DH, Tsiganos CP, Dalas E, Maniatis C, Koutsoukos PG (1993) Effect of proteoglycans on hydroxyapatite growth in vitro: the rol of hyaluronan. Biochem Biophys Acta 1153:129–136

    Google Scholar 

  • Pottenger LA, Lyon NB, Hecht JD, Neustadt PM, Robinson RA (1982) Influence of cartilage particle size and proteoglycan aggregation on immobilization of proteoglycans. J Biol Chem 257:11479–11485

    PubMed  Google Scholar 

  • Rauch U, Karthikeyan L, Maurel P, Margolis RU, Margolis RK (1992) Cloning and primary sequence of neurocan, a developmentally regulated, aggregating chondroitin sulfate proteoglycan of brain. J Biol Chem 267:19536–19547

    PubMed  Google Scholar 

  • Ripellino JA, Klinger MM, Margolis RU, Margolis RK (1985) The hyaluronic acid binding region as a specific probe for the localization of hyaluronic acid in tissue sections. Application to chick embryo and rat brain. J Histochem Cytochem 33:1060–1066

    PubMed  Google Scholar 

  • Säämänen A-M (1989) Articular cartilage proteoglycans and joint loading. A study in young rabbits and dogs. PhD thesis, University of Kuopio, Kuopio, Finland

    Google Scholar 

  • Säämänen A-M, Tammi M, Jurvelin J, Kiviranta I, Helminen HJ (1990) Proteoglycan alterations following immobilization and remobilization in the articular cartilage of young canine knee (stifle) joint. J Orthop Res 8:863–873

    PubMed  Google Scholar 

  • Tammi MI, Seppälä PO, Lehtonen A, Möttönen M (1978) Connective tissue components in normal and atherosclerotic human coronay arteries. Atherosclerosis 29:191–194

    PubMed  Google Scholar 

  • Tammi M, Säämänen A-M, Jauhiainen A, Malminen O, Kiviranta I, Helminen HJ (1983) Proteoglycan alterations in rabbit knee articular cartilage following physical exercise and immobilization. Connect Tissue Res 11:45–55

    PubMed  Google Scholar 

  • Tammi R, Ripellino JA, Margolis RU, Tammi M (1988) Localization of epidermal hyaluronic acid using the hyaluronate binding region of cartilage proteoglycan as a specific probe. J Invest Dermatol 90:412–414

    PubMed  Google Scholar 

  • Tammi R, Ågren UM, Tuhkanen A-L, Tammi M (1994) Hyaluronan metabolism in skin. Prog Histochem Cytochem 29:1–77

    Google Scholar 

  • Thonar EJ-MA, Sweet MBE, Immelman AR, Lyons G (1978) Hyaluronate in articular cartilage: age-related changes. Calcif Tissue Int 26:19–21

    Google Scholar 

  • Wisniewski HG, Maier R, Lotz M, Lee S, Klampfer L, Lee TH, Vilcek J (1993) TSG-6- a TNF-, IL-1-, and LPS-inducible secreted glycoprotein associated with arthritis. J Immunol 151: 6493–6601

    Google Scholar 

  • Wisniewski HG, Burgess WH, Oppenheim JD, Vilcek J (1994) TSG-6, an arthritis-associated hyaluronan binding protein, forms a stable complex with the serum protein inter-alpha-inhibitor. Biochemistry 33:7423–7429

    PubMed  Google Scholar 

  • Wusteman FS, Gillard GC (1977) Hyaluronic acid in clastic cartilage. Experientia 33:721–723

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Parkkinen, J.J., Häkkinen, T.P., Savolainen, S. et al. Distribution of hyaluronan in articular cartilage as probed by a biotinylated binding region of aggrecan. Histochem Cell Biol 105, 187–194 (1996). https://doi.org/10.1007/BF01462291

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01462291

Keywords

Navigation