Characterization of Autophagic Responses in Drosophila melanogaster

被引:11
|
作者
Xu, T. [1 ]
Kumar, S. [1 ]
Denton, D. [1 ]
机构
[1] Univ South Australia, Ctr Canc Biol, Adelaide, SA, Australia
关键词
PROGRAMMED CELL-DEATH; STARVATION-INDUCED AUTOPHAGY; FAT-BODY; QUANTITATIVE-ANALYSIS; ELECTRON-MICROSCOPY; STEROID REGULATION; GROWTH ARREST; CASPASE DRONC; PROTEIN; EXPRESSION;
D O I
10.1016/bs.mie.2016.09.089
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Drosophila is an excellent model system for studying autophagy during animal development due to the availability of genetic reagents and opportunity for in vivo cell biological analysis. The regulation and mechanism of autophagy are highly evolutionarily conserved and the role of autophagy has been characterized during various stages of Drosophila development as well as following starvation. Studies in Drosophila have revealed novel insights into the role of distinct components of the autophagy machinery. This chapter describes protocols for examining autophagy during Drosophila development. A crucial step in the induction of autophagy is the incorporation of Atg8a into the autophagosome. This can be measured as autophagic puncta using live fluorescent imaging, immunostaining, or immunoblot analysis of LC3/Atg8a processing. The level of autophagy can also be examined using other specific components of the autophagy pathway as markers detected by immunofluorescent imaging. Based on the distinct morphology of autophagy, it can also be examined by transmission electron microscopy. In addition, one of the advantages of using Drosophila as a model is the ability to undertake genetic analysis of individual components of the autophagy machinery. Current approaches that can be used to monitor autophagy, including the overall flux and individual steps in Drosophila melanogaster, will be discussed.
引用
收藏
页码:445 / 465
页数:21
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