## Abstract The possibility has been investigated that (1) the supplements required for the growth of the Madin Darby Canine Kidney (MDCK) cell line in serum‐free Medium K‐l are indeed requirements for the growth of normal kidney cells in vitro, and (2) that alterations in these growth requirements
Transport changes associated with growth control and malignant transformation
✍ Scribed by Michael J. Weber; Arthur H. Hale; Tom M. Yau; Trent Buckman; Marcia Johnson; Terrance M. Brady; Denise D. Larossa
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 911 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
We can distinguish two classes of membrane transport changes in cultured cells: (a) growth‐rate contingent changes are those which occur in coordination with the onset of density‐dependent inhibition of growth; (b) transformation‐specific changes are those which occur when cells become transformed, and which can be detected even when normal and transformed cells are growing at the same rate. Growth‐rate contingent changes include the density‐dependent changes in phosphate, nucleoside, glucose, amino acid, and potassium transport. Only one transformation‐specific transport change has been found in Rous‐transformed chicken embryo fibroblasts: an increased rate of hexose transport. The variations in potassium transport are associated with variations in the number of ouabain binding sites in the membrane. The molecular basis for changes in the rate of hexose transport is unknown, although gross changes in membrane bilayer composition and “fluidity” seem not to be involved. In analyzing the regulation of hexose transport activity, we find that decreased cAMP may play a role in the transformation‐specific increase in hexose transport, but that fibrinolytic activity is not necessary.
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