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PMID: 3194411 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Defining cellular senescence in IMR-90 cells: a flow cytometric analysis.

Sherwood SW, Rush D, Ellsworth JL, Schimke RT

Abstract

Using multiparameter flow cytometric analysis, we find that senescent cells accumulate in a unique cell-cycle compartment characterized in cell-cycle arrest in G1 and a significantly reduced nucleocytoplasmic ratio (genome size/cell mass) relative to cycling cells. With respect to gross cellular phenotype, the quiescent state of senescent cells differs from quiescence induced by density inhibition; the former is associated with a reduction in the nucleocytoplasmic ratio, while the latter is associated with an increase in the nucleocytoplasmic ratio. Senescent cells were present at all passages examined. The frequency of senescent cells was low in early-passage cultures and increased with passage number. Senescence of populations of IMR-90 cells reflects change in the relative frequency of these cells. The frequency of cells with karyotypic changes increased with the progressive accumulation of out-of-cycle cells.

MeSH Terms
Cell Cycle Cell Line Chromosome Aberrations DNA/analysis Flow Cytometry/methods Humans Karyotyping Ploidies
Chemicals
DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sherwood S W
Department of Biological Sciences, Stanford University, CA 94305.
Rush D
Ellsworth J L
Schimke R T
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1988-12-00
Pages
9086-90
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC282668
Subset
IM
Grants
NIA NIH HHS · AG-05568 · United States
NIGMS NIH HHS · GM-14931 · United States
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