LLC-PK(1) cells maintained in a new perfusion cell culture system exhibit an improved oxidative metabolism

Cell Physiol Biochem. 2002;12(2-3):153-62. doi: 10.1159/000063792.

Abstract

Cultured renal proximal tubule cells dedifferentiate from an oxidative metabolism to high rates of glycolysis over time. There are many reasons why cells in culture dedifferentiate, not least being a lack of homogenous nutrient supply and poor oxygenation. To this end we have developed a new cell culture device (EpiFlow), which combines continuous perfusion of medium with continuous oxygenation of cells grown on microporous supports. LLC-PK(1) cells cultured under EpiFlow conditions were compared with the same cells grown under conventional static conditions. EpiFlow maintained cells exhibited an improved oxidative metabolism as evidenced by 1) a decreased activity of glycolytic enzymes, 2) an increase in the activity of mitochondrial phosphate-dependent-glutaminase, 3) an increase in cellular ATP content, and 4) an improved morphology (increased cell height, mitochondrial density and an increased number and height of microvilli). In addition, LLC-PK(1) cells maintained under perfusion conditions exhibited an increased sensitivity to the respiratory chain blocker antimycin A as assayed by mitochondrial membrane potential (JC-1). We conclude that LLC-PK(1) cells maintained under EpiFlow conditions develop an improved oxidative metabolism that is more comparable to the in vivo situation.

MeSH terms

  • Animals
  • Cell Culture Techniques / instrumentation*
  • Cell Culture Techniques / methods*
  • Cell Extracts
  • Cell Size
  • Culture Media / chemistry
  • Glucose / metabolism
  • Glycolysis
  • LLC-PK1 Cells
  • Lactic Acid / metabolism
  • Microscopy, Electron
  • Oxygen / analysis
  • Oxygen / metabolism*
  • Perfusion / instrumentation*
  • Perfusion / methods*
  • Swine

Substances

  • Cell Extracts
  • Culture Media
  • Lactic Acid
  • Glucose
  • Oxygen