Article ID Journal Published Year Pages File Type
2040612 Cell Reports 2013 11 Pages PDF
Abstract

•A microfluidic device allows monitoring successive divisions of aging yeast cells•The entry into senescence follows an abrupt transition•The decline in mitochondrial membrane potential is an age-independent process

SummaryIn budding yeast, a mother cell can produce a finite number of daughter cells before it stops dividing and dies. Such entry into senescence is thought to result from a progressive decline in physiological function, including a loss of mitochondrial membrane potential (ΔΨ). Here, we developed a microfluidic device to monitor the dynamics of cell division and ΔΨ in real time at single-cell resolution. We show that cells do not enter senescence gradually but rather undergo an abrupt transition to a slowly dividing state. Moreover, we demonstrate that the decline in ΔΨ, which is observed only in a fraction of cells, is not responsible for entry into senescence. Rather, the loss of ΔΨ is an age-independent and heritable process that leads to clonal senescence and is therefore incompatible with daughter cell rejuvenation. These results emphasize the importance of quantitative single-cell measurements to decipher the causes of cellular aging.

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Related Topics
Life Sciences Agricultural and Biological Sciences Agricultural and Biological Sciences (General)
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