Transcriptome of microglia reveals a species-specific expression profile in bovines with conserved and new signature genes.


Journal

Glia
ISSN: 1098-1136
Titre abrégé: Glia
Pays: United States
ID NLM: 8806785

Informations de publication

Date de publication:
08 2021
Historique:
revised: 22 03 2021
received: 11 01 2021
accepted: 23 03 2021
pubmed: 4 4 2021
medline: 11 3 2022
entrez: 3 4 2021
Statut: ppublish

Résumé

Evidence is growing that microglia adopt different roles than monocyte-derived macrophages (MDM) during CNS injury. However, knowledge about their function in the pathogenesis of neuroinfections is only rudimentary. Cattle are frequently affected by neuroinfections that are either zoonotic or related to diseases in humans, and, hence, studies of bovine neuroinfections as a natural disease model may generate fundamental data on their pathogenesis potentially translatable to humans. We investigated the transcriptomic landscape and lineage markers of bovine microglia and MDM. Although bovine microglia expressed most microglial signature genes known from humans and mice, they exhibited a species-specific transcriptomic profile, including strikingly low expression of TMEM119 and enrichment of the two scavenger receptors MEGF10 and LY75. P2RY12 was amongst the most enriched genes in bovine microglia, and antibodies against P2RY12 labeled specifically resting microglia, but also reactive microglia within neuroinfection foci in-situ. On the other hand, F13A1 was amongst the most enriched genes in bovine monocytes and MDM and, additionally, the encoded protein was expressed in-situ in monocytes and MDM in the inflamed brain but not in microglia, making it a promising marker for infiltrating MDM in the brain. In culture, primary bovine microglia downregulated signature genes, expressed markers of activation, and converged their transcriptome to MDM. However, they retained several microglia signature genes that clearly distinguished them from bovine MDM, making them a promising in-vitro tool to study mechanisms of microglia-pathogen interactions.

Identifiants

pubmed: 33811399
doi: 10.1002/glia.24002
doi:

Substances chimiques

Megf10 protein, mouse 0
Membrane Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1932-1949

Informations de copyright

© 2021 Wiley Periodicals LLC.

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Auteurs

Leticia Tavares-Gomes (L)

Department of Clinical Research and Veterinary Public Health, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.

Camille Monney (C)

Department of Clinical Research and Veterinary Public Health, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Géraldine Neuhaus (G)

Department of Clinical Research and Veterinary Public Health, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

David Francisco (D)

Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.
Interfaculty of Bioinformatics Unit, University of Bern, Bern, Switzerland.
Swiss Institute of Bioinformatics, Switzerland.

Diana Solis (D)

Department of Clinical Research and Veterinary Public Health, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
University of Fribourg, Bern, Switzerland.

Artur Summerfield (A)

Faculty of Veterinary Medicine, Institute of Virology and Immunology, University of Bern, Bern, Switzerland.
Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Daniel Erny (D)

Institute of Neuropathology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Berta-Ottenstein-Programme, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Vidhya Jagannathan (V)

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Anna Oevermann (A)

Department of Clinical Research and Veterinary Public Health, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

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