A two-dimensional ERK-AKT signaling code for an NGF-triggered cell-fate decision. Academic Article uri icon

Overview

abstract

  • Growth factors activate Ras, PI3K, and other signaling pathways. It is not well understood how these signals are translated by individual cells into a decision to proliferate or differentiate. Here, using single-cell image analysis of nerve growth factor (NGF)-stimulated PC12 cells, we identified a two-dimensional phospho-ERK (pERK)-phospho-AKT (pAKT) response map with a curved boundary that separates differentiating from proliferating cells. The boundary position remained invariant when different stimuli were used or upstream signaling components perturbed. We further identified Rasa2 as a negative feedback regulator that links PI3K to Ras, placing the stochastically distributed pERK-pAKT signals close to the decision boundary. This allows for uniform NGF stimuli to create a subpopulation of cells that differentiates with each cycle of proliferation. Thus, by linking a complex signaling system to a simpler intermediate response map, cells gain unique integration and control capabilities to balance cell number expansion with differentiation.

publication date

  • December 28, 2011

Research

keywords

  • Cell Differentiation
  • Cell Proliferation
  • Extracellular Signal-Regulated MAP Kinases
  • MAP Kinase Signaling System
  • Nerve Growth Factor
  • Proto-Oncogene Proteins c-akt

Identity

PubMed Central ID

  • PMC3897208

Scopus Document Identifier

  • 84856264773

Digital Object Identifier (DOI)

  • 10.1016/j.molcel.2011.11.023

PubMed ID

  • 22206868

Additional Document Info

volume

  • 45

issue

  • 2