Proliferation is required for induction of terminal differentiation of Friend erythroleukemia cells

1992 ◽  
Vol 70 (7) ◽  
pp. 555-564 ◽  
Author(s):  
Louaine L. Spriggs ◽  
Steven M. Hill ◽  
James R. Jeter Jr.

The relationship between cell proliferation and differentiation has long been a source of controversy. Stimulation of normal erythroid maturation results in a finite number of cell divisions accompanied by a concomitant accumulation of hemoglobin. Friend erythroleukemia cells treated with hexamethylene bisacetamide differentiate in a similar manner, while agents such as hemin apparently induce differentiation without limiting cell proliferation. Aphidicolin, an inhibitor of DNA synthesis, has been reported to induce differentiation in the absence of cell proliferation. Using these three chemicals we have investigated the relationship between cell proliferation and erythrocytic maturation by exposing Friend erythroleukemia cells to either hexamethylene bisacetamide (5 mM), hemin (100 μM), or aphidicolin 1.2 μM) and examining the effects on cell growth, morphology, and hemoglobin production. Proliferation in the presence of hexamethylene bisacetamide is limited to four to five rounds of cell division, while hemin has no inhibitory effect. Hexamethylene bisacetamide initiates the complete erythrocytic maturation program, including cellular structural changes and hemoglobin synthesis. Hemin stimulates only globin gene transcription, not differentiation. Aphidicolin inhibits cell growth within 24 h, but does not induce differentiation. Furthermore, inhibition of proliferation by aphidicolin prevents subsequent hexamethylene bisacetamide induced differentiation. These results indicate that at least one round of cell division is required for initiation of erythrocytic differentiation.Key words: proliferation, erythrocytic differentiation, hexamethylene bisacetamide, hemin, aphidicolin.

Blood ◽  
1980 ◽  
Vol 55 (3) ◽  
pp. 501-504 ◽  
Author(s):  
SE Steinberg ◽  
CL Campbell ◽  
PS Rabinovitch ◽  
RS Hillman

Abstract Cultures of Friend erythroleukemia cells were subjected to the antibiotics trimethoprim (T) and sulfamethoxazole (S) at levels equal to or below the usual therapeutic range. At T 8 microgram/ml and S 40 microgram/ml, cell growth was arrested, cells appeared megaloblastic, and the examination of cell-cycle distribution by flow microfluorimetry revealed arrest in S phase. With a tenfold reduction in drug levels (T, 08 microgram/ml; S, 4 microgram/ml) cell growth was less markedly inhibited, morphology remained megaloblastic, and S-phase block was still dramatic. A further tenfold reduction (T, 0.08 microgram/ml; S, 0.4 microgram/ml), well below effective antibacterial levels, allowed normal cell growth and morphology but DNA synthesis was still inhibited. Additions of folinic acid at 100 ng/ml averted all drug effects. Thus T/S can affect cell replication even at levels well below those usually employed and could prolong the rate of recovery of hematopoietic cells in the myelosuppressed patient.


1966 ◽  
Vol 53 (2) ◽  
pp. 189-204 ◽  
Author(s):  
R. Seifert ◽  
H. Hilz

ABSTRACT 1 × 10−6 M cortisol produces an immediate block in cell division in L cells (mouse fibroblasts) propagated in suspension culture. Under these conditions no inhibition of metabolic parameters could be observed (except for a partial inhibition of DNA synthesis). Consequently, there is an increase in cell size which is accompanied by an increased DNA content and an elevated capacity of these cells to incorporate sulphate into a sulphopolysaccharide and proline into the protein fraction respectively. The cortisol-induced inhibition of cell proliferation and the increase in cell size are reversible on withdrawal of the hormone from the medium.


1999 ◽  
Vol 246 (2) ◽  
pp. 348-354 ◽  
Author(s):  
Conrad M. Mallia ◽  
Victoria Aguirre ◽  
Eric McGary ◽  
Yan Tang ◽  
Aline B. Scandurro ◽  
...  

1990 ◽  
Vol 68 (7-8) ◽  
pp. 1052-1056 ◽  
Author(s):  
B. S. Beckman ◽  
J. R. Jeter Jr.

Endogenous arachidonic acid metabolism and protein phosphorylation have been examined in Friend erythroleukemia cells in response to the induction of differentiation by dimethyl sulfoxide and hexamethylene bisacetamide. 15-Hydroxyeicosatetraenoic acid levels were elevated in cells differentiated with hexamethylene bisacetamide or dimethyl sulfoxide compared with undifferentiated cells. Protein phosphorylation decreased markedly in differentiated cells compared with undifferentiated cells and the addition of 15-hydroperoxyeicosatetraenoic acid specifically decreased the phosphorylation of a 28-kilodalton protein. These findings indicate that products of 15-lipoxygenase may act as intracellular messengers in Friend erythroleukemia cells by affecting protein phosphorylation.Key words: arachidonic acid, protein phosphorylation, proliferation, differentiation, 15-lipoxygenase.


1978 ◽  
Vol 111 (2) ◽  
pp. 269-276 ◽  
Author(s):  
Alan F. Lau ◽  
Raymond W. Ruddon ◽  
Marc S. Collett ◽  
Anthony J. Faras

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