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ContactJ: Lipid droplets-mitochondria contacts characterization through fluorescence microscopy and image analysis [version 1; peer review: 2 approved with reservations]

Authors :
Gemma Martín
Marta Bosch
Elisenda Coll
Robert G. Parton
Albert Pol
Maria Calvo
Author Affiliations :
<relatesTo>1</relatesTo>Advanced Optical Microscopy Facility. Scientific and Technological Centers, University of Barcelona, Barcelona, 08036, Spain<br /><relatesTo>2</relatesTo>Biomedicine Department. School of Medicine, University of Barcelona, Barcelona, 08036, Spain<br /><relatesTo>3</relatesTo>Cell Compartments and Signaling Group, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, 08036, Spain<br /><relatesTo>4</relatesTo>Institute for Molecular Bioscience (IMB), University of Queensland, Brisbane, Queensland, 4072, Australia<br /><relatesTo>5</relatesTo>Centre for Microscopy and Microanalysis, University of Queensland, Brisbane, Queensland, 4072, Australia<br /><relatesTo>6</relatesTo>Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, 08010, Spain
Source :
F1000Research. 10:263
Publication Year :
2021
Publisher :
London, UK: F1000 Research Limited, 2021.

Abstract

Lipid droplets (LDs) are the major lipid storage organelles of eukaryotic cells and together with mitochondria key regulators of cell bioenergetics. LDs communicate with mitochondria and other organelles forming “metabolic synapse” contacts to ensure that lipid supply occurs where and when necessary. Although transmission electron microscopy analysis allows an accurate and precise analysis of contacts, the characterization of a large number of cells and conditions can become a long-term process. In order to extend contact analysis to hundreds of cells and multiple conditions, we have combined confocal fluorescence microscopy with advanced image analysis methods. In this work, we have developed the ImageJ macro script ContactJ, a novel and straight image analysis method to identify and quantify contacts between LD and mitochondria in fluorescence microscopy images allowing the automatic analysis. This image analysis workflow combines colocalization and skeletonization methods, enabling the quantification of LD-mitochondria contacts together with a complete characterization of organelles and cellular parameters. The correlation and normalization of these parameters contribute to the complex description of cell behavior under different experimental energetic states. ContactJ is available here: https://github.com/UB-BioMedMicroscopy/ContactJ/tree/1.0

Details

ISSN :
20461402
Volume :
10
Database :
F1000Research
Journal :
F1000Research
Notes :
[version 1; peer review: 2 approved with reservations]
Publication Type :
Academic Journal
Accession number :
edsfor.10.12688.f1000research.51900.1
Document Type :
software-tool
Full Text :
https://doi.org/10.12688/f1000research.51900.1