Brainstem local microglia induce whisker map plasticity in the thalamus after peripheral nerve injury

Summary: Whisker deafferentation in mice disrupts topographic connectivity from the brainstem to the thalamic ventral posteromedial nucleus (VPM), which represents whisker map, by recruiting “ectopic” axons carrying non-whisker information in VPM. However, mechanisms inducing this plasticity remain...

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Main Authors: Yoshifumi Ueta, Mariko Miyata
Format: Article
Language:English
Published: Elsevier 2021-03-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124721001376
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spelling doaj-b5df21788e0047a389c1c3c59bb84d6e2021-03-11T04:24:39ZengElsevierCell Reports2211-12472021-03-013410108823Brainstem local microglia induce whisker map plasticity in the thalamus after peripheral nerve injuryYoshifumi Ueta0Mariko Miyata1Division of Neurophysiology, Department of Physiology, School of Medicine, Tokyo Women’s Medical University, Tokyo 162-8666, Japan; Corresponding authorDivision of Neurophysiology, Department of Physiology, School of Medicine, Tokyo Women’s Medical University, Tokyo 162-8666, Japan; Corresponding authorSummary: Whisker deafferentation in mice disrupts topographic connectivity from the brainstem to the thalamic ventral posteromedial nucleus (VPM), which represents whisker map, by recruiting “ectopic” axons carrying non-whisker information in VPM. However, mechanisms inducing this plasticity remain largely unknown. Here, we show the role of region-specific microglia in the brainstem principal trigeminal nucleus (Pr5), a whisker sensory-recipient region, in VPM whisker map plasticity. Systemic or local manipulation of microglial activity reveals that microglia in Pr5, but not in VPM, are necessary and sufficient for recruiting ectopic axons in VPM. Deafferentation causes membrane hyperexcitability of Pr5 neurons dependent on microglia. Inactivation of Pr5 neurons abolishes this somatotopic reorganization in VPM. Additionally, microglial depletion prevents deafferentation-induced ectopic mechanical hypersensitivity. Our results indicate that local microglia in the brainstem induce peripheral nerve injury-induced plasticity of map organization in the thalamus and suggest that microglia are potential therapeutic targets for peripheral nerve injury-induced mechanical hypersensitivity.http://www.sciencedirect.com/science/article/pii/S2211124721001376brainstemmap plasticitymechanical hypersensitivitymicrogliamouseperipheral nerve injury
collection DOAJ
language English
format Article
sources DOAJ
author Yoshifumi Ueta
Mariko Miyata
spellingShingle Yoshifumi Ueta
Mariko Miyata
Brainstem local microglia induce whisker map plasticity in the thalamus after peripheral nerve injury
Cell Reports
brainstem
map plasticity
mechanical hypersensitivity
microglia
mouse
peripheral nerve injury
author_facet Yoshifumi Ueta
Mariko Miyata
author_sort Yoshifumi Ueta
title Brainstem local microglia induce whisker map plasticity in the thalamus after peripheral nerve injury
title_short Brainstem local microglia induce whisker map plasticity in the thalamus after peripheral nerve injury
title_full Brainstem local microglia induce whisker map plasticity in the thalamus after peripheral nerve injury
title_fullStr Brainstem local microglia induce whisker map plasticity in the thalamus after peripheral nerve injury
title_full_unstemmed Brainstem local microglia induce whisker map plasticity in the thalamus after peripheral nerve injury
title_sort brainstem local microglia induce whisker map plasticity in the thalamus after peripheral nerve injury
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2021-03-01
description Summary: Whisker deafferentation in mice disrupts topographic connectivity from the brainstem to the thalamic ventral posteromedial nucleus (VPM), which represents whisker map, by recruiting “ectopic” axons carrying non-whisker information in VPM. However, mechanisms inducing this plasticity remain largely unknown. Here, we show the role of region-specific microglia in the brainstem principal trigeminal nucleus (Pr5), a whisker sensory-recipient region, in VPM whisker map plasticity. Systemic or local manipulation of microglial activity reveals that microglia in Pr5, but not in VPM, are necessary and sufficient for recruiting ectopic axons in VPM. Deafferentation causes membrane hyperexcitability of Pr5 neurons dependent on microglia. Inactivation of Pr5 neurons abolishes this somatotopic reorganization in VPM. Additionally, microglial depletion prevents deafferentation-induced ectopic mechanical hypersensitivity. Our results indicate that local microglia in the brainstem induce peripheral nerve injury-induced plasticity of map organization in the thalamus and suggest that microglia are potential therapeutic targets for peripheral nerve injury-induced mechanical hypersensitivity.
topic brainstem
map plasticity
mechanical hypersensitivity
microglia
mouse
peripheral nerve injury
url http://www.sciencedirect.com/science/article/pii/S2211124721001376
work_keys_str_mv AT yoshifumiueta brainstemlocalmicrogliainducewhiskermapplasticityinthethalamusafterperipheralnerveinjury
AT marikomiyata brainstemlocalmicrogliainducewhiskermapplasticityinthethalamusafterperipheralnerveinjury
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