LC3- and p62-based biochemical methods for the analysis of autophagy progression in mammalian cells

Methods. 2015 Mar:75:13-8. doi: 10.1016/j.ymeth.2014.11.021. Epub 2014 Dec 5.

Abstract

Autophagy is an intracellular degradation system that delivers cytoplasmic materials to the lysosome or vacuole. This system plays a crucial role in various physiological and pathological processes in living organisms ranging from yeast to mammals. Thus, an accurate and reliable measure of autophagic activity is necessary. However, autophagy involves dynamic and complicated processes that make it difficult to analyze. The term "autophagic flux" is used to denote overall autophagic degradation (i.e., delivery of autophagic cargo to the lysosome) rather than autophagosome formation. Immunoblot analysis of LC3 and p62/SQSTM1, among other proteins, has been widely used to monitor autophagic flux. Here, we describe basic protocols to measure the levels of endogenous LC3 and p62 by immunoblotting in cultured mammalian cells.

Keywords: Autophagic flux; Autophagy; Immunoblotting; LC3; SQSTM1; p62.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics*
  • Adaptor Proteins, Signal Transducing / metabolism
  • Animals
  • Autophagy / genetics*
  • Cell Line
  • Heat-Shock Proteins / genetics*
  • Heat-Shock Proteins / metabolism
  • Lysosomes / genetics
  • Lysosomes / metabolism
  • Mammals
  • Mice
  • Microtubule-Associated Proteins / genetics*
  • Microtubule-Associated Proteins / metabolism
  • Molecular Biology / methods*
  • Sequestosome-1 Protein

Substances

  • Adaptor Proteins, Signal Transducing
  • Heat-Shock Proteins
  • Map1lc3b protein, mouse
  • Microtubule-Associated Proteins
  • Sequestosome-1 Protein
  • Sqstm1 protein, mouse