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PMID: 19200872 Published · ppublish English Journal Article

Monitoring autophagy in mammalian cultured cells through the dynamics of LC3.

Methods in enzymology ·Vol. 452 ·2009-00-00 ·Pages 1-12

Kimura S, Fujita N, Noda T, Yoshimori T

Abstract

In this chapter, we introduce several methods that rely on the analysis of LC3, a versatile marker protein of autophagic structures in mammalian cultured cells. The appearance of LC3-positive puncta is indicative of the induction of autophagy, and it is observed either by immunofluorescence or by GFP-based microscopy. The maturation process by which autophagosomes are converted into autolysosomes can be monitored by the GFP and RFP tandemly tagged LC3 (tfLC3) method. Lysosomal turnover of LC3 is a good index of the proceeding of autophagy and can be assessed by Western blotting. These methods will provide a relatively easy assessment of autophagy, and the details of the procedure will be described along with possible pitfalls.

MeSH Terms
Autophagy Cells, Cultured/metabolism Fluorescent Antibody Technique Green Fluorescent Proteins/genetics,metabolism HeLa Cells Humans Microtubule-Associated Proteins/genetics,metabolism
Chemicals
MAP1LC3A protein, human Microtubule-Associated Proteins Green Fluorescent Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kimura Shunsuke
Department of Cellular Regulation, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Fujita Naonobu
Noda Takeshi
Yoshimori Tamotsu
Article Info
Journal
Methods in enzymology
Abbr.
Methods Enzymol
ISSN
1557-7988
Published
2009-00-00
Pages
1-12
Language
English
Region
United States
NLM ID
0212271
Subset
IM
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