Oscillations of the p53-Akt network: implications on cell survival and death

Keng Boon Wee1, Uttam Surana, Baltazar D Aguda

  • 1Institute of Molecular and Cell Biology, A*STAR (Agency for Science, Technology and Research), Proteos, Singapore.

Plos One
|February 7, 2009
PubMed

Insights

Ionizing radiation (IR) exposure causes oscillations in p53 and MDM2 protein levels. These oscillations regulate cell fate decisions, lowering the threshold for switching from survival to apoptosis.

Area of Science:

  • Molecular Biology
  • Cellular Signaling
  • Radiation Biology

Background:

  • Intracellular protein levels of p53 and MDM2 oscillate post-ionizing radiation (IR).
  • The p53-MDM2 feedback loop and p53-AKT antagonism drive cellular state switching.
  • The physiological role of p53/MDM2 oscillations is not fully understood.

Purpose of the Study:

  • Investigate the physiological significance of p53 and MDM2 oscillations.
  • Determine how these oscillations impact the p53-AKT network's switching behavior.
  • Elucidate the role of oscillations in cell fate determination after IR.

Main Methods:

  • Computational modeling of the p53-AKT network.
  • Analysis of p53 and MDM2 protein level dynamics.
  • Assessment of p53-target gene expression.

Main Results:

  • The p53-AKT network model reproduces experimentally observed p53 and MDM2 oscillations upon IR exposure.
  • Oscillations decrease the IR threshold for switching from a pro-survival to a pro-apoptotic state.
  • Oscillatory p53 induces higher p53-target gene expression than non-oscillatory p53.

Conclusions:

  • p53/MDM2 oscillations are integral to the p53-AKT network's response to IR.
  • Oscillations modulate cell fate decisions by altering the pro-survival/pro-apoptotic switch.
  • These findings provide insight into DNA damage response and cell death pathways.

Related Concept Videos

DNA Damage Can Stall the Cell Cycle02:36

DNA Damage Can Stall the Cell Cycle

In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
DNA Damage can Stall the Cell Cycle02:36

DNA Damage can Stall the Cell Cycle

In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
Interactions Between Signaling Pathways01:19

Interactions Between Signaling Pathways

Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a rapamycin-insensitive companion...
Negative Regulator Molecules01:23

Negative Regulator Molecules

Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.