Proteoglycan metabolism of equine articular chondrocytes cultured in alginate beads.
Abstract: Equine chondrocytes were cultured in vitro for 30 days in ionically gelled alginate beads. The alginate polymerises into a stable gel in the presence of divalent cations (calcium), and rapid depolymerisation in the presence of a calcium chelator releases the viable chondrocytes. The chondrocytes maintained a spherical appearance for 30 days in culture, in marked contrast to monolayer cultures, which develop a dedifferentiated fibroblastic morphology. The major proteoglycan molecule produced by the encapsulated chondrocytes was aggrecan, of similar hydrodynamic size to aggrecan molecules present in the matrix of the articular cartilage from which the cells were harvested. Link protein, keratan sulphate and chondroitin sulphate were also synthesised by the chondrocytes, as demonstrated by immunohistochemistry. The proteoglycan secreted by the chondrocytes consisted of at least two pools, one remaining adjacent to the cell and forming a dense, cell-associated matrix, and another migrating more peripherally into the intercellular compartment. Newly synthesised proteoglycans extracted from the pericellular matrix and the intercellular matrix were similar in hydrodynamic size and aggregated in the presence of exogenous hyaluronan.
Publication Date: 1997-01-01 PubMed ID: 9160423DOI: 10.1016/s0034-5288(97)90178-8Google Scholar: Lookup
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- Journal Article
Summary
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This research explores the metabolism of proteoglycan in horse cartilage cells, which were grown in a stable substance called alginate beads for a month. The study provides insights into how the cells behaved in this environment and verifies the production of important components, highlighting two particular patterns of proteoglycan secretion by the cells.
Research Methodology
- Equine or horse cartilage cells were grown in vitro, or outside the living body, in what is known as ‘alginate beads’. Alginate is a material that turns into a stable gel when exposed to divalent cations like calcium.
- These cartilage cells were cultured in this environment for a period of 30 days. In contrast to other methods of culture, such as monolayer cultures, the cartilage cells maintained a spherical shape.
Significant Findings
- The primary proteoglycan molecule produced by the cartilage cells grown in this manner was aggrecan, which was similar in structure and size to aggrecan present in the natural cartilage matrix from where the cells were harvested.
- Other substances synthesized by the cartilage cells were link proteins, keratan sulphate, and chondroitin sulphate. This was established through a technique called immunohistochemistry, which uses antibodies to detect specific molecules in cell or tissue sections.
- There were two distinct pools where the proteoglycan released by the cartilage cells. One remained adjacent to the cell and formed a dense matrix. The other moved more peripherally into the region between cells, termed the intercellular compartment.
Important Deductions
- New proteoglycans extracted from the matrix around the cell and the intercellular matrix, were comparable in size. They also have the ability to aggregate or cluster together when external hyaluronan, a substance found in connective, epithelial and neural tissues, is present. This finding suggests a consistency in the properties and behavior of these newly synthesized proteoglycans.
- Overall, the research provides valuable insights into the behavior and metabolism of equine chondrocytes under particular conditions. It could prove crucial for future studies related to cartilage health and disease.
Cite This Article
APA
Platt D, Wells T, Bayliss MT.
(1997).
Proteoglycan metabolism of equine articular chondrocytes cultured in alginate beads.
Res Vet Sci, 62(1), 39-47.
https://doi.org/10.1016/s0034-5288(97)90178-8 Publication
Researcher Affiliations
- Royal Veterinary College, University of London, Hertfordshire.
MeSH Terms
- Alginates
- Animals
- Autoradiography / veterinary
- Calcium / pharmacology
- Cartilage, Articular / cytology
- Cartilage, Articular / metabolism
- Cell Division / drug effects
- Cell Division / physiology
- Cells, Cultured
- Chondroitin Sulfates / metabolism
- Horses / metabolism
- Immunohistochemistry
- Keratan Sulfate / metabolism
- Microspheres
- Phenotype
- Proteoglycans / biosynthesis
- Proteoglycans / chemistry
- Proteoglycans / metabolism
Citations
This article has been cited 3 times.- Kurz B, Lange T, Voelker M, Hart ML, Rolauffs B. Articular Cartilage-From Basic Science Structural Imaging to Non-Invasive Clinical Quantitative Molecular Functional Information for AI Classification and Prediction. Int J Mol Sci 2023 Oct 7;24(19).
- Liu W, Madry H, Cucchiarini M. Application of Alginate Hydrogels for Next-Generation Articular Cartilage Regeneration. Int J Mol Sci 2022 Jan 20;23(3).
- Hernandez PA, Jacobsen TD, Barati Z, Chahine NO. Confocal scanning of intervertebral disc cells in 3D: Inside alginate beads and in native microenvironment. JOR Spine 2020 Dec;3(4):e1106.
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