scholarly journals Oxygen-sensitive stages of the cell cycle of human diploid cells.

1978 ◽  
Vol 78 (2) ◽  
pp. 390-400 ◽  
Author(s):  
A K Balin ◽  
D B Goodman ◽  
H Rasmussen ◽  
V J Cristofalo

We had established that growth of human diploid WI-38 cells is reversibly inhibited by elevated partial pressures of oxygen (PO2) and we were interested in determining where in the cell cycle growth was delayed. A technique combining cytospectrophotometry and autoradiography was used to determine cell cycle parameters. Confluent cells that were subcultivated and exposed to a PO2 of 365 +/- 8 mm Hg were delayed primarily after DNA synthesis but before metaphase. At a PO2 of 590 +/- 35 mm Hg, most cells did not initiate DNA synthesis, and the few that did, failed to complete the process. When exponentially growing cells that had already begun DNA synthesis were exposed to a PO2 of 590 p 35 mm Hg, they accumulated after completing DNA synthesis but before initiating mitosis. The rate at which (3H)thymidine was incorporated into DNA was inversely correlated with oxygen tension (PO2 of 135--590 mm Hg). These results suggest that the process most sensitive to oxygen causes cells to be delayed after DNA synthesis but before metaphase. Slightly higher PO2's were needed to inhibit the initiation of DNA synthesis. Further, the rate of DNA synthesis is decreased by elevated oxygen tensions.

1982 ◽  
Vol 94 (1) ◽  
pp. 187-192 ◽  
Author(s):  
G C Burmer ◽  
C J Zeigler ◽  
T H Norwood

Previous studies have shown that the senescent phenotype is dominant with respect to DNA synthesis in fusions between late passage and actively replicating human diploid fibroblasts. Brief postfusion treatments with the protein synthesis inhibitor cycloheximide (CHX) or puromycin have been found to significantly delay (by 24-48 h) the inhibition of entry into DNA synthesis of young nuclei in heterokaryons after fusion with senescent cells. A significant fraction of the senescent nuclei incorporated tritiated thymidine in CHX-treated heterokaryons. The optimal duration of exposure to CHX was 1-3 h immediately after fusion, although treatments beginning as late as 9 h after fusion elevated the heterokaryon labeling index. Prefusion treatments with CHX were without a significant effect. These results are consistent with the interpretation that regulatory cell cycle inhibitor(s) which are dependent upon protein synthesis may be present in heterokaryons between senescent and actively replicating cells.


1963 ◽  
Vol 16 (1) ◽  
pp. 202-209 ◽  
Author(s):  
P. S. Moorhead ◽  
Vittorio Defendi

1977 ◽  
Vol 74 (1) ◽  
pp. 58-67 ◽  
Author(s):  
A K Balin ◽  
D B Goodman ◽  
H Rasmussen ◽  
V J Cristofalo

Human diploid cells (WI-38) were serially subcultivated at partial pressures of oxygen (Po2) ranging from 5.6 mm Hg to 608 mm Hg. At a Po2 of 5.6 mm Hg, the number of doublings to phase out was less than that of control cells at a Po2 of 137 mm Hg. Cultures grown at Po2's of 24, 49, or 137 mm Hg grew at the same rate and phased out after a similar number of population doublings. Population lifespan was markedly shortened by chronic exposure to elevated Po2's, a phenomenon that was, in part, reversible. d-1-alpha-Tocopherol (10 microgram/ml or 100 microgram/ml) homogenized into the medium at each weekly subcultivation did not extend the lifespan of cells at reduced, ambient, or elevated oxygen tensions. These results indicate that neither oxygen toxicity nor free radical reactions play a significant role in limiting the lifespan of WI-38 cells grown in vitro under ambient oxygen tensions (Po2 137 mm Hg).


1979 ◽  
Vol 34 (3) ◽  
pp. 328-334 ◽  
Author(s):  
T. Matsumura ◽  
Z. Zerrudo ◽  
L. Hayflick

1983 ◽  
Vol 143 (2) ◽  
pp. 343-349 ◽  
Author(s):  
Toshinori Ide ◽  
Yoshiaki Tsuji ◽  
Sadahiko Ishibashi ◽  
Youji Mitsui

Nature ◽  
1968 ◽  
Vol 218 (5146) ◽  
pp. 1064-1065 ◽  
Author(s):  
JOHN B. LITTLE

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