Dimethylsulfoxide (DMSO) converts almost all of the undifferentiated murine erythroleukemia cells (MEL or Friend cells, clone 745A) in a culture to differentiated cells that contain high levels of hemoglobin and that stop growing after a limited number of cell divisions. Contrary to other reports-th
Folate utilization in friend erythroleukemia cells
β Scribed by Stephen E. Steinberg; Susan Fonda; Caryl L. Campbell; Robert S. Hillman
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 528 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
In order to study the generation, factors controlling endogenous folate pools, and their functional importance, Friend erythroleukemia cells were grown in media containing 100; 1,000; and 10,000 ng/ml of tritiated pteroylglutamic acid (^3^H)PteGIu~1~ and then studied in unlabeled media with varying amounts of PteGlu~1~. The intracellular folate pool was directly proportional to the PteGlu~1~ in which the cells were incubated. At equilibrium, greater than 95% of the labeled intracellular folate pool chromatographed as polyglutamyl folate, regardless of the exogenous folate concentration. The functional importance of the intracellular folate pool was studied by varying the endogenous pool and the exogenous (media) supply. The ability of the cells to replicate in the absence of exogenous folate was directly proportional to the intracellular polyglutamyl folate pool. The maximal rate of replication, however, required exogenous PteGlu~1~ in addition. The cell doubling time was the most important determinant of intracellular folate turnover; changes in the intracellular pool size and the extracellular folate concentration had no effect on the turnover time. In a rapidly proliferating tissue, the onset of functional folate deficiency will be determined by dilution of intracellular polyglutamates among progeny until a critical level is reached.
π SIMILAR VOLUMES
Friend erythroleukemia cells (FELC) served as a model system for cell differentiation because these cells can be triggered to differentiate by a variety of chemical agents. Treatment with the classical inducer of differentiation, hexamethylene bisacetamide (HMBA), stimulated superoxide dismutase (SO
## Abstract Three cell lines of mouse erythroleukemia transformed by Friend virus (FLC), namely 745, F4β1, and 3BMβ78, were grown for six days in the absence or in the presence of 1.5% (v/v) dimethylsulfoxide (DMSO) and compared cytochemically for naphtolβAS Dβchloroacetate esterase (E), alkalineph
## Abstract The relationship between tumorigenicity and __in vitro__ differentiation was studied in four Friend erythroβleukemia cell lines. The cell lines were isolated by repeated subcloning of an unmutagenized population (sib selection). The cell lines differed in their ability to form tumors wh