Spontaneous Cell Competition in Immortalized Mammalian Cell Lines.

PLoS One

Departments of Medicine and Cell and Developmental Biology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, United States of America; Abramson Family Cancer Research Institute, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.

Published: May 2016

AI Article Synopsis

  • Cell competition is a process where more fit cells eliminate less fit ones through direct interactions, specifically observed in commonly used mammalian cell lines like U2OS, 3T3, and MDCK.
  • This competition leads to cell death only when the fitter and less fit cells are cultured together, relying on caspase activity and physical contact between the cells.
  • The findings suggest that cellular metabolism plays a key role in how these cells assess each other's fitness levels, indicating that cell competition is a prevalent phenomenon in in vitro studies of immortalized mammalian cells.

Article Abstract

Cell competition is a form of cell-cell interaction by which cells compare relative levels of fitness, resulting in the active elimination of less-fit cells, "losers," by more-fit cells, "winners." Here, we show that in three routinely-used mammalian cell lines - U2OS, 3T3, and MDCK cells - sub-clones arise stochastically that exhibit context-dependent competitive behavior. Specifically, cell death is elicited when winner and loser sub-clones are cultured together but not alone. Cell competition and elimination in these cell lines is caspase-dependent and requires cell-cell contact but does not require de novo RNA synthesis. Moreover, we show that the phenomenon involves differences in cellular metabolism. Hence, our study demonstrates that cell competition is a common feature of immortalized mammalian cells in vitro and implicates cellular metabolism as a mechanism by which cells sense relative levels of "fitness."

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511643PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0132437PLOS

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