Characterization of microglia behaviour in healthy and pathological conditions with image analysis tools

Author:

Martinez Aleix1,Hériché Jean-Karim2ORCID,Calvo Maria3,Tischer Christian4ORCID,Otxoa-de-Amezaga Amaia5,Pedragosa Jordi67,Bosch Anna3,Planas Anna M.67,Petegnief Valérie67ORCID

Affiliation:

1. Institute for Bioengineering of Catalonia, 08028 Barcelona, Spain

2. Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany

3. Advanced Optical Microscopy Facility, Scientific and Technological Centers. School of Medicine, University of Barcelona, 08036 Barcelona, Spain

4. Centre for BioImage Analysis, European Molecular Biology Laboratory, 69117 Heidelberg, Germany

5. Achucarro Basque Center for Neuroscience and Department of Neuroscience, University of the Basque Country UPV/EHU, Achucarro, 48940 Leioa, Spain

6. Department of Neuroscience and Experimental Therapeutics, Institute for Biomedical Research of Barcelona, Spanish Research Council, 08036 Barcelona, Spain

7. Institut d'Investigacions Biomèdiques Augustí Pi i Sunyer, 08036 Barcelona, Spain

Abstract

Microglia are very sensitive to changes in the environment and respond through morphological, functional and metabolic adaptations. To depict the modifications microglia undergo under healthy and pathological conditions, we developed free access image analysis scripts to quantify microglia morphologies and phagocytosis. Neuron–glia cultures, in which microglia express the reporter tdTomato, were exposed to excitotoxicity or excitotoxicity + inflammation and analysed 8 h later. Neuronal death was assessed by SYTOX staining of nucleus debris and phagocytosis was measured through the engulfment of SYTOX + particles in microglia. We identified seven morphologies: round, hypertrophic, fried egg, bipolar and three ‘inflamed’ morphologies. We generated a classifier able to separate them and assign one of the seven classes to each microglia in sample images. In control cultures, round and hypertrophic morphologies were predominant. Excitotoxicity had a limited effect on the composition of the populations. By contrast, excitotoxicity + inflammation promoted an enrichment in inflamed morphologies and increased the percentage of phagocytosing microglia. Our data suggest that inflammation is critical to promote phenotypical changes in microglia. We also validated our tools for the segmentation of microglia in brain slices and performed morphometry with the obtained mask. Our method is versatile and useful to correlate microglia sub-populations and behaviour with environmental changes.

Funder

Ministerio de Ciencia e Innovación

European Commission

Eusko Jaurlaritza

Publisher

The Royal Society

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,General Neuroscience

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