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Journal ArticleDOI

Relationship between cell shape and type of collagen synthesised as chondrocytes lose their cartilage phenotype in culture

Klaus von der Mark, +3 more
- 09 Jun 1977 - 
- Vol. 267, Iss: 5611, pp 531-532
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TLDR
It is found that there is no strict correlation between cell morphology and type of collagen synthesised in cartilage colonies kept in monolayer culture at low density.
Abstract
WHEN chondrocytes from sternal or articular cartilage are kept in monolayer culture at low density, they eventually lose their cartilage phenotype1–4. Within four passages or approximately 1 month in culture they change from a polygonal or round to a flattened, amoeboid-like shape5–7, and instead of cartilage collagen (type II collagen8) they synthesise the genetically different type I collagen. It is not known whether there is a strict correlation between the occurrence of cell flattening and the change in collagen synthesis within individual cells. We have reported that preferentially flattened, fibroblast-like cells at the edge of cartilage colonies synthesise type I collagen, whereas round or polygonal chondrocytes generally synthesise type II collagen1–3. The change is nearly complete in a culture at a time when excessive flattening is observed4. Using an immunofluorescence double staining technique9,10, we have now found that there is no strict correlation between cell morphology and type of collagen synthesised.

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Citations
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Journal ArticleDOI

Stimulation of type II collagen biosynthesis and secretion in bovine chondrocytes cultured with degraded collagen

TL;DR: Results clearly indicate a stimulatory effect of degraded collagen on the type II collagen biosynthesis of chondrocytes and suggest a possible feedback mechanism for the regulation of collagen turnover in cartilage tissue.
Journal ArticleDOI

Hypoxia promotes the differentiated human articular chondrocyte phenotype through SOX9-dependent and -independent pathways.

TL;DR: Results show that hypoxia has a broader beneficial effect on the chondrocyte phenotype than has been previously described, and HIF-2α may represent a new and promising therapeutic target for cartilage repair.
Patent

Systems and methods for isolating and using clinically safe adipose derived regenerative cells

TL;DR: In this article, automated systems and methods are described that separate regenerative cells, e.g., stem and/or progenitor cells, from adipose tissue, i.e., from a wide variety of tissues.
Journal ArticleDOI

Synthesis of cartilage matrix by mammalian chondrocytes in vitro. II. Maintenance of collagen and proteoglycan phenotype.

TL;DR: The results demonstrate the long-term in vitro phenotypic stability of the bovine articular chondrocytes and the advantages of the in vitro system as a model for studying the effects of external agents, such as drugs and vitamins.
Journal ArticleDOI

Micromass co-culture of human articular chondrocytes and human bone marrow mesenchymal stem cells to investigate stable neocartilage tissue formation in vitro.

TL;DR: In this paper, the effect of chondrogenic stimuli on articular cartilage defects was investigated in micromass pellets with and without TGF-beta1 and dexamethasone (±T±D) factors.
References
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Journal ArticleDOI

Study of differential collagen synthesis during development of the chick embryo by immunofluorescence. I. Preparation of collagen type I and type II specific antibodies and their application to early stages of the chick embryo.

TL;DR: Specific antibodies against skin and bone collagen and cartilage collagen are prepared for the study of differential collagen synthesis during development of the chick embryo by immunofluorescence.
Journal ArticleDOI

Changes in type of collagen synthesized as clones of chick chondrocytes grow and eventually lose division capacity.

TL;DR: Analysis of collagen type at each successive subculture until the time of cellular senescence has shown that a change in synthesis occurs from the cartilage-specific Type II collagen to a mixture of Type I collagen and the Type I trimer.
Journal ArticleDOI

The loss of phenotypic traits by differentiated cells. VI. Behavior of the progeny of a single chondrocyte.

TL;DR: If the progeny of a single, genetically programmed chondrocyte may or may not synthesize chondroitin sulfate, then extragenic sites in the cytoplasm or cell surface must influence the decision as to which cluster of "luxur" molecules the cell will synthesize.
Journal ArticleDOI

Simultaneous synthesis of types I and III collagen by fibroblasts in culture.

TL;DR: Specific antibodies against types I and III collagens and procollagens were used to localize these proteins in cultured human cells and indicate that the same cell makes both proteins.
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