Using MitER for 3D analysis of mitochondrial morphology and ER contacts

被引:2
|
作者
Kichuk, Therese [1 ]
Dhamankar, Satyen [2 ]
Malani, Saurabh [2 ]
Hofstadter, William A. [1 ]
Wegner, Scott A. [1 ]
Cristea, Ileana M. [1 ]
Avalos, Jose L. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[2] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ 08544 USA
[3] Princeton Univ, Andlinger Ctr Energy & Environm, Princeton, NJ 08544 USA
[4] Princeton Univ, High Meadows Environm Inst, Princeton, NJ 08544 USA
[5] Princeton Univ, Omenn Darling Bioengn Inst, Princeton, NJ 08544 USA
来源
CELL REPORTS METHODS | 2024年 / 4卷 / 01期
基金
美国国家卫生研究院;
关键词
CP: Imaging; image analysis; imaging; inter-organelle contact; mitochondrial-ER contact; organelle distribution; organelle morphology; Saccharomyces cerevisea;
D O I
10.1016/j.crmeth.2023.100692
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have developed an open -source workflow that allows for quantitative single -cell analysis of organelle morphology, distribution, and inter -organelle contacts with an emphasis on the analysis of mitochondria and mitochondria-endoplasmic reticulum (mito-ER) contact sites. As the importance of inter -organelle contacts becomes more widely recognized, there is a concomitant increase in demand for tools to analyze subcellular architecture. Here, we describe a workflow we call MitER (pronounced "mightier"), which allows for automated calculation of organelle morphology, distribution, and inter -organelle contacts from 3D renderings by employing the animation software Blender. We then use MitER to quantify the variations in the mito-ER networks of Saccharomyces cerevisiae, revealing significantly more mito-ER contacts within respiring cells compared to fermenting cells. We then demonstrate how this workflow can be applied to mammalian systems and used to monitor mitochondrial dynamics and inter -organelle contact in time-lapse studies.
引用
收藏
页数:17
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