Isolation of Lysosomes from Mammalian Tissues and Cultured Cells

Methods Mol Biol. 2016:1449:299-311. doi: 10.1007/978-1-4939-3756-1_19.

Abstract

Lysosomes participate within the cells in the degradation of organelles, macromolecules, and a wide variety of substrates. In any study on specific roles of lysosomes, both under physiological and pathological conditions, it is advisable to include methods that allow their reproducible and reliable isolation. However, purification of lysosomes is a difficult task, particularly in the case of cultured cells. This is mainly because of the heterogeneity of these organelles, along with their low number and high fragility. Also, isolation methods, while disrupting plasma membranes, have to preserve the integrity of lysosomes, as the breakdown of their membranes releases enzymes that could damage all cell organelles, including themselves. The protocols described below have been routinely used in our laboratory for the specific isolation of lysosomes from rat liver, NIH/3T3, and other cultured cells, but can be adapted to other mammalian tissues or cell lines.

Keywords: Cultured cells; Differential and gradient centrifugation; Liver; Lysosomes; Subcellular fractionation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Fractionation / methods*
  • Cell Line
  • Cell Membrane
  • Cells, Cultured
  • Centrifugation, Density Gradient / methods
  • Liver / cytology
  • Lysosomes
  • Mice
  • Organelles / metabolism*
  • Rats
  • Subcellular Fractions / metabolism