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K J Andersen

Publications and source records attributed to K J Andersen.

74 records · Page 5Linked to original sources

Multicellular tumor spheroids in serum-free culture.

The serum-free culture of multicellular tumor spheroids from two rat (BT4c, BT5c) and two human (GaMg, D-54Mg) glioma cell lines is described. The spheroids were propagated in two different chemically defined media, showing differences in growth requirements between the human and rat cell lines. The spheroids from all the cell lines showed reduced growth rate as compared to spheroids maintained in serum supplemented culture. A change in spheroid morphology was observed for the D-54Mg cell line, indicated by a reduced occurrence of microvilli, increased pyknosis and cellular granularity. The other spheroids maintained their morphology in serum-free culture. For the D-54 Mg spheroids, flow cytometric DNA measurements showed that the serum-free growth conditions caused a drop in the DNA S-phase (6.4% vs. 12.3% in serum supplemented cultures). The cell cycle distribution was unchanged for the other cell lines tested. The present study provides the basis for using multicellular tumor spheroids in biological studies which are dependent on a detailed control with chemical environment.

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Characteristics of human and rat glioma cells grown in a defined medium.

Human (D54Mg, GaMg) and rat (BT5C, BT4Cn) glioma cells cultured in a chemically defined medium showed reduced growth when compared to serum-supplemented medium. The BT5C cells changed from a flat epithelioid morphology to a more glia-like structure. The serum-free medium caused an aggregation of BT5C cells which spontaneously lost anchorage dependence and continued to grow in suspension as multicellular tumor spheroids. The BT4Cn and human cell lines did not show any change in morphology. Flow cytometric DNA measurements showed no change in ploidy for cells grown in serum-free medium. Cell cycle analysis revealed that the same proportion of cells were proliferating (S and G2M phase cells) in serum-free medium as compared to serum-supplemented medium. The reduced growth is probably due to increased cell cycle time.

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