| Literature DB >> 27730609 |
Chihiro Takatsuka1, Yuko Inoue-Aono2, Yuji Moriyasu3.
Abstract
Autolysosomes are organelles that sequester and degrade a portion of the cytoplasm during autophagy. Although autophagosomes are short lived compared to other organelles such as mitochondria, plastids, and peroxisomes, many autolysosomes accumulate in tobacco BY-2 cells cultured under sucrose starvation conditions in the presence of a cysteine protease inhibitor. We here describe our methodology for isolating autolysosomes from BY-2 cells by conventional cell fractionation using a Percoll gradient. The autolysosome fraction separates clearly from fractions containing mitochondria and peroxisomes. It contains acid phosphatase, vacuolar H+-ATPase, and protease activity. Electron micrographs show that the fraction contains partially degraded cytoplasm seen in autolysosomes before isolation although an autolysosome structure is only partially preserved.Entities:
Keywords: Acid phosphatase; Autolysosome; Autophagy; Cysteine protease inhibitor; H+-ATPase; Protease; Protein degradation; Sucrose starvation; Vacuole
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Year: 2017 PMID: 27730609 DOI: 10.1007/978-1-4939-6533-5_12
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745