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Establishment and Characterization of Cell Lines from the Walker Carcinoma 256 Able to Grow in Suspension Culture and Deficient in Thymidine Kinase
Francisco Arvelo, Auri Yabrudi, Maria Elena Delgado and Néstor González-Cadavid
Vol. 20, No. 7 (Jul., 1984), pp. 549-565
Published by: Society for In Vitro Biology
Stable URL: http://www.jstor.org/stable/4292847
Page Count: 17
You can always find the topics here!Topics: Cell lines, NIH 3T3 cells, Cultured cells, HeLa cells, Tumors, Tumor cell line, Cell growth, Cell culture techniques, Ascites, Rats
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A cell line from the Walker carcinosarcoma 256 of the rat has been established in suspension culture in medium with 5% bovine calf serum for over 350 generations, with an average population doubling time of 17 h, a plating efficiency of 56%, a colony forming efficiency of 32%, and a good capacity to form colonies in soft agar. The cells are morphologically indistinguishable from those in the solid tumor and ascites as checked by transmission and scanning electron microscopy. The karyotype is characterized by a modal number of 65 chromosomes and by the presence of a marker metacentric chromosome. The cells express thymidine kinase, γ-glutamyl transpeptidase, and alkaline phosphatase; are agglutinable by concanavalin A; and can be synchronized by the triple thymidine block. They induce primary tumors, both subcutaneously (solid) and intraperitoneally (ascitic), in the rat; are able to metastasize upon injection by the tail vein; and invade the chorioallantoic membrane of the chick embryo. Cells in suspension can be transferred to monolayers, considerably decreasing their tumorigenicity without affecting the other parameters studied, and can be switched back to suspension culture. DNA-mediated transfection showed that DNA from these cells can transform the NIH-3T3 line. Upon growth of the monolayers in a BrdUr-containing medium, a sub-line was established that was cloned into a thymidine kinase-deficient line unable to grow in HAT medium and with properties otherwise similar to those of the parental wild type cells.
In Vitro © 1984 Society for In Vitro Biology