Profiling Microglia in a Mouse Model of Machado–Joseph Disease
Ana Bela Campos,
Sara Duarte-Silva,
Bruno Fernandes,
Sofia Pereira das Neves,
Fernanda Marques,
Andreia Teixeira-Castro,
Andreia Neves-Carvalho,
Daniela Monteiro-Fernandes,
Camila Cabral Portugal,
Renato Socodato,
Teresa Summavielle,
António Francisco Ambrósio,
João Bettencourt Relvas,
Patrícia Maciel
Affiliations
Ana Bela Campos
Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal
Sara Duarte-Silva
Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal
Bruno Fernandes
Department of Informatics, ALGORITMI Center, University of Minho, 4710-057 Braga, Portugal
Sofia Pereira das Neves
Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal
Fernanda Marques
Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal
Andreia Teixeira-Castro
Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal
Andreia Neves-Carvalho
Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal
Daniela Monteiro-Fernandes
Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal
Camila Cabral Portugal
Glial Cell Biology Group, Instituto de Investigação e Inovação em Saúde (i3S), Instituto de Biologia Molecular e Celular (IBMC), University of Porto, 4200-135 Porto, Portugal
Renato Socodato
Glial Cell Biology Group, Instituto de Investigação e Inovação em Saúde (i3S), Instituto de Biologia Molecular e Celular (IBMC), University of Porto, 4200-135 Porto, Portugal
Teresa Summavielle
Addiction Biology Group, Instituto de Investigação e Inovação em Saúde (i3S), Instituto de Biologia Molecular e Celular (IBMC), University of Porto, 4200-135 Porto, Portugal
António Francisco Ambrósio
Coimbra Institute for Clinical and Biomedical Research (iCBR), Faculty of Medicine, Univiversity of Coimbra, 3004-504 Coimbra, Portugal
João Bettencourt Relvas
Glial Cell Biology Group, Instituto de Investigação e Inovação em Saúde (i3S), Instituto de Biologia Molecular e Celular (IBMC), University of Porto, 4200-135 Porto, Portugal
Patrícia Maciel
Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal
Microglia have been increasingly implicated in neurodegenerative diseases (NDs), and specific disease associated microglia (DAM) profiles have been defined for several of these NDs. Yet, the microglial profile in Machado–Joseph disease (MJD) remains unexplored. Here, we characterized the profile of microglia in the CMVMJD135 mouse model of MJD. This characterization was performed using primary microglial cultures and microglial cells obtained from disease-relevant brain regions of neonatal and adult CMVMJD135 mice, respectively. Machine learning models were implemented to identify potential clusters of microglia based on their morphological features, and an RNA-sequencing analysis was performed to identify molecular perturbations and potential therapeutic targets. Our findings reveal morphological alterations that point to an increased activation state of microglia in CMVMJD135 mice and a disease-specific transcriptional profile of MJD microglia, encompassing a total of 101 differentially expressed genes, with enrichment in molecular pathways related to oxidative stress, immune response, cell proliferation, cell death, and lipid metabolism. Overall, these results allowed us to define the cellular and molecular profile of MJD-associated microglia and to identify genes and pathways that might represent potential therapeutic targets for this disorder.