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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

Chitosan-alginate as scaffolding material for cartilage tissue engineering.

TL;DR: It is suggested that chitosan-alginate scaffolds promote cell proliferation, enhance phenotype expression of HTB-94 chondrocytes, and may potentially serve as an improved alternative to chitOSan scaffolds for cartilage tissue engineering.
Journal ArticleDOI

Regulated production of mineralization-competent matrix vesicles in hypertrophic chondrocytes.

TL;DR: The findings reveal that hypertrophic chondrocytes can qualitatively modulate their production of matrix vesicles and only when induced to initiate mineralization, will release mineralization-competent matrixVesicles rich in annexin V and alkaline phosphatase.
Journal ArticleDOI

Chondrocyte dedifferentiation and osteoarthritis (OA)

TL;DR: Molecular knowledge underlying dedifferentiation process is presented, connections between dedifferentiated-like and OA are emphasized and therapeutic strategies aiming at the maintenance of chondrogenic phenotype are considered.
Journal ArticleDOI

Collagen in tissue-engineered cartilage: types, structure, and crosslinks.

TL;DR: It is found that differentiated chondrocyte‐polymer constructs are capable of forming a complex structure of collagen matrix in vitro, producing a tissue similar to natural articular cartilage on an ultrastructural scale.
Journal ArticleDOI

Enhanced repair of articular cartilage defects in vivo by transplanted chondrocytes overexpressing insulin-like growth factor I (IGF-I).

TL;DR: The data indicate that allogeneic chondrocytes, transfected by a nonviral method and cultured in alginate, are able to secrete biologically relevant amounts of IGF-I over a prolonged period of time in vitro and suggest that therapeutic growth factor gene delivery using encapsulated and transplanted genetically modified chondROcytes may be applicable to sites of focal articular cartilage damage.
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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