## Abstract The transport and phosphorylation of 2‐deoxy‐D‐glucose are separate and sequential events in both normal and virus‐transformed 3T3 cells. The apparent enhancement of 2‐dOG uptake by 3T3 cells accompanying virus transformation is not due to an effect on the transport process but to enhan
Variation in potassium transport properties of mouse 3T3 cells as a result of subcultivation
✍ Scribed by Joseph T. Tupper
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 467 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Unidirectional potassium influx and the fraction of this influx sensitive to ouabain, an inhibitor of the (Na + K) activated ATPase, have been evaluated as a function of subcultivation of the 3T3 and SV40 transformed 3T3 cell. Total and ouabain‐sensitive K influx change little over approximately 50 passages of the transformed 3T3 cell. In contrast, these components of K influx increase nearly 5‐fold over a similar number of passages of the 3T3 cell. During early passages total and ouabain‐sensitive K influx of the 3T3 cell are below that of the SV40 3T3 cell on a per cell volume basis. At later passages the magnitude of these components of K transport exceed those found in the SV40 3T3 cell. Previous studies have reported the ouabain‐sensitive uptake of K and the levels of (Na + K) activated ATPase as being higher, lower or equivalent in the 3T3 versus transformed 3T3 cell. The present data suggest these differences may result from the degree to which the cells were passaged at the time of the experiments. Evaluation of previous studies substantiates this conclusion.
📜 SIMILAR VOLUMES
Eight phthalate esters, with alcohol chain lengths of 1-11 carbon atoms and with various degrees of branching, were tested in vitro in the L5178Y mouse lymphoma mammalian cell mutation assay and in the Balb/3T3 cell transformation assay. The tests were performed as part of a voluntary testing agreem
Bone metabolism is often affected by a variety of mechanical forces, but the cytological basis of their action is not knomn. In this study, we examined the effect of a continuously applied compressive pressure (CCP) on the growth and differentiation of clonal mouse osteoblast-like cells (MC3T3-El) c
## Abstract Changing the medium, or adding fresh serum, induces a large proportion of the proliferatively quiescent cells in confluent monolayers of human WI‐38 and mouse BALB/3T3 cells to initiate a growth‐division cycle. Exposure at the time of the medium change or serum addition to MGBG (methyl