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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

Osteoarthritis-derived chondrocytes are a potential source of multipotent progenitor cells for cartilage tissue engineering

TL;DR: It is concluded that chondrogenic capacity is not significantly affected by OA, and OACs could be a potential source of multipotent progenitor cells for cartilage tissue engineering.
Journal ArticleDOI

Laser sintered porous polycaprolacone scaffolds loaded with hyaluronic acid and gelatin-grafted thermoresponsive hydrogel for cartilage tissue engineering

TL;DR: It is concluded that the laser-sintered porous PCL scaffold has good cytocompatibility, and that the hydrogel phase is able to enhance initial chondrocytes attachment as well as GAG and collagen production of chondROcytes.
Journal ArticleDOI

Comparing effects of perfusion and hydrostatic pressure on gene profiles of human chondrocyte.

TL;DR: Both HPP and P treatment had beneficial effects on chondrocyte differentiation and decreased catabolic enzyme expression, providing new insight into how hydrostatic pressure and perfusion enhance cartilage differentiation and inhibit catabolic effects.
Journal ArticleDOI

Adhesion characteristics of chondrocytes cultured separately and in co-cultures with synovial fibroblasts.

TL;DR: Investigating the adherence mechanism(s) and behaviour of cultured chondrocytes under various culturing conditions, co‐culturing with fibroblasts, or growth in the presence of conditioned medium indicates that chONDrocyte time‐adhesion curves and the final percentiles of attached cells to a plastic substrate are much slower and lower respectively than those of anchorage dependent cell types.
Journal ArticleDOI

Evidence That Rat Chondrocytes Can Differentiate Into Perichondrial Cells

TL;DR: It is suggested that epiphyseal chondrocytes of postnatal animals retain the potential to differentiate into perichondrial cells, supporting the hypothesis that theperichondrium originates from collagen type II‐expressing chondROcytes at the periphery of the cartilaginous bone template.
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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