A three-dimensional collagen network for cartilage reconstruction

Development ◽  
1971 ◽  
Vol 26 (2) ◽  
pp. 157-167
Author(s):  
S. Moskalewski ◽  
M. Kamiński ◽  
A. Dukwicz

To obtain a three-dimensional network which would support cells during culture, cold collagen solution was mixed with cells and converted into a gel at 37 °C. Gelation of collagen did not influence cell viability. The development of chondrocyte cultures in collagen gels depended on the distance between the cells. Single chondrocytes were surrounded by a mucopolysaccharide ring. The collagen fibres in parts of the cultures with moderate cell density were strongly alcian-blue-positive. Chondrocytes in crowded areas of cultures formed a cartilage matrix. Collagen gel with Ehrlich ascites tumour cells and liver cells remained unchanged after cultivation. Cultures of kidney cells and some chondrocyte cultures shrivelled, owing to partial collagen digestion. The delicate primary collagen network in some cultures partially transformed to much thicker, long fibres or to distinct capsules around chondrocytes.

1984 ◽  
Vol 68 (1) ◽  
pp. 227-241
Author(s):  
W.S. Haston ◽  
J.M. Shields

In this paper we propose that the constriction ring, a prominent feature of moving leucocytes, is a major source of locomotive force. Analysis of time-lapse films of lymphocytes in suspension and moving through three-dimensional collagen gels, demonstrated that the constriction ring was the morphological manifestation of a wave of circular contraction that moved antero-posteriorly. In lymphocytes in suspension the wave moved, although the cells could not. Analysis of lymphocytes moving through a collagen gel revealed that the waves remained stationary with respect to the external environment while the cell appeared to move forward through them. Passage of a single equatorial contraction wave resulted in cell lengthening: a shortening of the region posterior to the constriction was observed in cells moving through collagen gels, but not in lymphocytes held in suspension, suggesting that attachment of cells to the collagen network was necessary for longitudinal contraction. Lymphocyte attachment to collagen gels was mediated through the rapid extension of bleb-like structures into the collagen network. Transmission electron microscopy (TEM) failed to demonstrate any organized structure at the constriction ring. NBD-Phallacidin staining of lymphocytes together with TEM demonstrated that F-actin was distributed evenly throughout the length of the cell. Cell polarity was clearly recognizable by the distribution of coated vesicles, microvilli, and all organelles to the rear, and Thy 1–2 to the front, of motile cells, but polarity could be reversed by the passage of a single contraction wave starting at the rear of the cell, without prior redistribution of these structures.


1976 ◽  
Vol 160 (1) ◽  
pp. 121-123 ◽  
Author(s):  
T L Spencer

The transport and oxidation of succinate by functionally intact Ehrlich ascites-tumour cells was investigated. On the basis of pH dependence and inhibitor sensitivity it was concluded that succinate may be transported across the cell membrane by the organic anion carrier system. Thus the ability of isolated Ehrlich cells to oxidize succinate is real, and is not necessarily a result of damage to cell integrity.


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