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PMID: 7505784 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Internalization of hyaluronan by chondrocytes occurs via receptor-mediated endocytosis.

Journal of cell science ·Vol. 106 ( Pt 1) ·1993-09-00 ·Pages 365-75

Hua Q, Knudson CB, Knudson W

Abstract

Several studies have suggested that chondrocytes must have the capacity to internalize and degrade extracellular hyaluronan. In the present study we show direct evidence that hyaluronan is, in fact, endocytosed by chondrocytes and that the endocytosis is mediated via cell surface CD44/hyaluronan receptors. Cultures of bovine articular chondrocytes as well as rat chondrosarcoma chondrocytes were incubated with either fluorescein- or 3H-labeled hyaluronan. Intense binding and accumulation of labeled hyaluronan was visualized by fluorescence microscopy or bright-field/dark-field microscopy following autoradiography. Cell surface hyaluronan was removed with either trypsin or Streptomyces hyaluronidase in order to distinguish and quantify intracellular endocytosed hyaluronan. Labeled hyaluronan was visualized within small discrete intracellular vesicles distributed throughout the cytoplasm. Binding and endocytosis of fluorescein- or 3H-labeled hyaluronan was totally blocked by the addition of excess unlabeled hyaluronan or hyaluronan hexasaccharides, competitive inhibitors of hyaluronan/hyaluronan receptor interactions. Binding and endocytosis was also blocked by the addition of anti-CD44 monoclonal antibodies. Characterization of endocytosed 3H-labeled hyaluronan demonstrated that a significant portion of the hyaluronan was degraded by both the bovine articular and rat chondrosarcoma chondrocytes. Interestingly, a higher proportion of bound hyaluronan was internalized by the bovine chondrocytes. Therefore, hyaluronan receptor-mediated endocytosis and degradation of hyaluronan may provide a critical link to the maintenance and homeostasis of cartilage tissue.

MeSH Terms
Animals Antibodies, Monoclonal/immunology,pharmacology Carrier Proteins/immunology,metabolism Cartilage, Articular/cytology Cattle Cells, Cultured Chondrosarcoma Endocytosis/drug effects Hyaluronan Receptors Hyaluronic Acid/metabolism Rats Receptors, Cell Surface/immunology,metabolism Receptors, Lymphocyte Homing/immunology,metabolism Tumor Cells, Cultured
Chemicals
Antibodies, Monoclonal Carrier Proteins Hyaluronan Receptors Receptors, Cell Surface Receptors, Lymphocyte Homing Hyaluronic Acid
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hua Q
Department of Biochemistry, Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois 60612.
Knudson C B
Knudson W
Article Info
Journal
Journal of cell science
Abbr.
J Cell Sci
ISSN
0021-9533
Published
1993-09-00
Pages
365-75
Language
English
Region
England
NLM ID
0052457
Subset
IM
Grants
NIAMS NIH HHS · R01 AR039507 · United States
NIAMS NIH HHS · AR39239 · United States
NIAMS NIH HHS · AR39507 · United States
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