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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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Bridging the Gap: From 2D Cell Culture to 3D Microengineered Extracellular Matrices

TL;DR: How the field of engineered extracellular matrices has evolved with the development of new hydrogel chemistry and the maturation of micro‐ and nano‐ fabrication is explored.
Journal ArticleDOI

iPS cell technologies and cartilage regeneration.

TL;DR: One important application of the iPSC technology is modeling cartilage diseases, such as skeletal dysplasia, and chondrogenically differentiated iPSCs generated from patients would recapitulate the pathology and may serve as a useful platform both for exploring the disease mechanisms and for drug screening.
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Yes-associated protein (YAP) is a negative regulator of chondrogenesis in mesenchymal stem cells.

TL;DR: In developing mouse limbs, Yap was nuclear in the perichondrium while mostly phosphorylated and cytosolic in cells of the cartilage anlage, suggesting downregulation of Yap co-transcriptional activity during physiological chondrogenesis in vivo.
Journal ArticleDOI

Rac1/Cdc42 and RhoA GTPases Antagonistically Regulate Chondrocyte Proliferation, Hypertrophy, and Apoptosis

TL;DR: It is shown that the small GTPases, Rac1 and Cdc42, accelerate the rate of chondrocyte differentiation and apoptosis, thereby antagonizing the activity of RhoA.
Journal ArticleDOI

Vulnerability to ROS-induced cell death in ageing articular cartilage: the role of antioxidant enzyme activity.

TL;DR: Substantial loss of chondrocytes occurs in rat articular cartilage which may result from increased vulnerability to elevated intracellular ROS levels, consequent upon a decline in antioxidant defence.
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.
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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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