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Differential Roles of TREM2+ Microglia in Anterograde and Retrograde Axonal Injury Models

Microglia are the main immune cells of the central nervous system (CNS), and they are devoted to the active surveillance of the CNS during homeostasis and disease. In the last years, the microglial receptor Triggering Receptor Expressed on Myeloid cells-2 (TREM2) has been defined to mediate several...

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Autores principales: Manich, Gemma, Gómez-López, Ariadna Regina, Almolda, Beatriz, Villacampa, Nàdia, Recasens, Mireia, Shrivastava, Kalpana, González, Berta, Castellano, Bernardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715005/
https://www.ncbi.nlm.nih.gov/pubmed/33328887
http://dx.doi.org/10.3389/fncel.2020.567404
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author Manich, Gemma
Gómez-López, Ariadna Regina
Almolda, Beatriz
Villacampa, Nàdia
Recasens, Mireia
Shrivastava, Kalpana
González, Berta
Castellano, Bernardo
author_facet Manich, Gemma
Gómez-López, Ariadna Regina
Almolda, Beatriz
Villacampa, Nàdia
Recasens, Mireia
Shrivastava, Kalpana
González, Berta
Castellano, Bernardo
author_sort Manich, Gemma
collection PubMed
description Microglia are the main immune cells of the central nervous system (CNS), and they are devoted to the active surveillance of the CNS during homeostasis and disease. In the last years, the microglial receptor Triggering Receptor Expressed on Myeloid cells-2 (TREM2) has been defined to mediate several microglial functions, including phagocytosis, survival, proliferation, and migration, and to be a key regulator of a new common microglial signature induced under neurodegenerative conditions and aging, also known as disease-associated microglia (DAM). Although microglial TREM2 has been mainly studied in chronic neurodegenerative diseases, few studies address its regulation and functions in acute inflammatory injuries. In this context, the present work aims to study the regulation of TREM2 and its functions after reparative axonal injuries, using two-well established animal models of anterograde and retrograde neuronal degeneration: the perforant pathway transection (PPT) and the facial nerve axotomy (FNA). Our results indicate the appearance of a subpopulation of microglia expressing TREM2 after both anterograde and retrograde axonal injury. TREM2+ microglia were not directly related to proliferation, instead, they were associated with specific recognition and/or phagocytosis of myelin and degenerating neurons, as assessed by immunohistochemistry and flow cytometry. Characterization of TREM2+ microglia showed expression of CD16/32, CD68, and occasional Galectin-3. However, specific singularities within each model were observed in P2RY12 expression, which was only downregulated after PPT, and in ApoE, where de novo expression was detected only in TREM2+ microglia after FNA. Finally, we report that the pro-inflammatory or anti-inflammatory cytokine microenvironment, which may affect phagocytosis, did not directly modify the induction of TREM2+ subpopulation in any injury model, although it changed TREM2 levels due to modification of the microglial activation pattern. In conclusion, we describe a unique TREM2+ microglial subpopulation induced after axonal injury, which is directly associated with phagocytosis of specific cell remnants and show different phenotypes, depending on the microglial activation status and the degree of tissue injury.
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spelling pubmed-77150052020-12-15 Differential Roles of TREM2+ Microglia in Anterograde and Retrograde Axonal Injury Models Manich, Gemma Gómez-López, Ariadna Regina Almolda, Beatriz Villacampa, Nàdia Recasens, Mireia Shrivastava, Kalpana González, Berta Castellano, Bernardo Front Cell Neurosci Cellular Neuroscience Microglia are the main immune cells of the central nervous system (CNS), and they are devoted to the active surveillance of the CNS during homeostasis and disease. In the last years, the microglial receptor Triggering Receptor Expressed on Myeloid cells-2 (TREM2) has been defined to mediate several microglial functions, including phagocytosis, survival, proliferation, and migration, and to be a key regulator of a new common microglial signature induced under neurodegenerative conditions and aging, also known as disease-associated microglia (DAM). Although microglial TREM2 has been mainly studied in chronic neurodegenerative diseases, few studies address its regulation and functions in acute inflammatory injuries. In this context, the present work aims to study the regulation of TREM2 and its functions after reparative axonal injuries, using two-well established animal models of anterograde and retrograde neuronal degeneration: the perforant pathway transection (PPT) and the facial nerve axotomy (FNA). Our results indicate the appearance of a subpopulation of microglia expressing TREM2 after both anterograde and retrograde axonal injury. TREM2+ microglia were not directly related to proliferation, instead, they were associated with specific recognition and/or phagocytosis of myelin and degenerating neurons, as assessed by immunohistochemistry and flow cytometry. Characterization of TREM2+ microglia showed expression of CD16/32, CD68, and occasional Galectin-3. However, specific singularities within each model were observed in P2RY12 expression, which was only downregulated after PPT, and in ApoE, where de novo expression was detected only in TREM2+ microglia after FNA. Finally, we report that the pro-inflammatory or anti-inflammatory cytokine microenvironment, which may affect phagocytosis, did not directly modify the induction of TREM2+ subpopulation in any injury model, although it changed TREM2 levels due to modification of the microglial activation pattern. In conclusion, we describe a unique TREM2+ microglial subpopulation induced after axonal injury, which is directly associated with phagocytosis of specific cell remnants and show different phenotypes, depending on the microglial activation status and the degree of tissue injury. Frontiers Media S.A. 2020-11-20 /pmc/articles/PMC7715005/ /pubmed/33328887 http://dx.doi.org/10.3389/fncel.2020.567404 Text en Copyright © 2020 Manich, Gómez-López, Almolda, Villacampa, Recasens, Shrivastava, González and Castellano. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular Neuroscience
Manich, Gemma
Gómez-López, Ariadna Regina
Almolda, Beatriz
Villacampa, Nàdia
Recasens, Mireia
Shrivastava, Kalpana
González, Berta
Castellano, Bernardo
Differential Roles of TREM2+ Microglia in Anterograde and Retrograde Axonal Injury Models
title Differential Roles of TREM2+ Microglia in Anterograde and Retrograde Axonal Injury Models
title_full Differential Roles of TREM2+ Microglia in Anterograde and Retrograde Axonal Injury Models
title_fullStr Differential Roles of TREM2+ Microglia in Anterograde and Retrograde Axonal Injury Models
title_full_unstemmed Differential Roles of TREM2+ Microglia in Anterograde and Retrograde Axonal Injury Models
title_short Differential Roles of TREM2+ Microglia in Anterograde and Retrograde Axonal Injury Models
title_sort differential roles of trem2+ microglia in anterograde and retrograde axonal injury models
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715005/
https://www.ncbi.nlm.nih.gov/pubmed/33328887
http://dx.doi.org/10.3389/fncel.2020.567404
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