The cultural divide: exponential growth in classical 2D and metabolic equilibrium in 3D environments

PLoS One. 2014 Sep 15;9(9):e106973. doi: 10.1371/journal.pone.0106973. eCollection 2014.

Abstract

Introduction: Cellular metabolism can be considered to have two extremes: one is characterized by exponential growth (in 2D cultures) and the other by a dynamic equilibrium (in 3D cultures). We have analyzed the proteome and cellular architecture at these two extremes and found that they are dramatically different.

Results: Structurally, actin organization is changed, microtubules are increased and keratins 8 and 18 decreased. Metabolically, glycolysis, fatty acid metabolism and the pentose phosphate shunt are increased while TCA cycle and oxidative phosphorylation is unchanged. Enzymes involved in cholesterol and urea synthesis are increased consistent with the attainment of cholesterol and urea production rates seen in vivo. DNA repair enzymes are increased even though cells are predominantly in Go. Transport around the cell--along the microtubules, through the nuclear pore and in various types of vesicles has been prioritized. There are numerous coherent changes in transcription, splicing, translation, protein folding and degradation. The amount of individual proteins within complexes is shown to be highly coordinated. Typically subunits which initiate a particular function are present in increased amounts compared to other subunits of the same complex.

Summary: We have previously demonstrated that cells at dynamic equilibrium can match the physiological performance of cells in tissues in vivo. Here we describe the multitude of protein changes necessary to achieve this performance.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Cell Communication
  • Cell Culture Techniques*
  • Cell Physiological Phenomena
  • Cell Proliferation
  • Cells, Cultured
  • Chromatography, Liquid
  • Hep G2 Cells
  • Humans
  • Metabolome*
  • Microtubules / metabolism
  • Microtubules / ultrastructure
  • Proteome*
  • Tandem Mass Spectrometry

Substances

  • Actins
  • Proteome

Grants and funding

University of Southern Denmark. MC2 Biotek. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.