A novel injury paradigm in the central nervous system of adult Drosophila: molecular, cellular and functional aspects

The mammalian central nervous system (CNS) exhibits limited regenerative capacity and the mechanisms that mediate its regeneration are not fully understood. Here, we present a novel experimental design to damage the CNS by using a contusion injury paradigm. The design of this protocol allows the stu...

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Main Authors: María Losada-Pérez, Nuria García-Guillén, Sergio Casas-Tintó
Format: Article
Language:English
Published: The Company of Biologists 2021-05-01
Series:Disease Models & Mechanisms
Subjects:
jnk
Online Access:http://dmm.biologists.org/content/14/5/dmm044669
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spelling doaj-3fafc87b45aa4b52ad37fdf7c52d17f02021-06-20T11:55:53ZengThe Company of BiologistsDisease Models & Mechanisms1754-84031754-84112021-05-0114510.1242/dmm.044669044669A novel injury paradigm in the central nervous system of adult Drosophila: molecular, cellular and functional aspectsMaría Losada-Pérez0Nuria García-Guillén1Sergio Casas-Tintó2 Instituto Cajal-CSIC, Department of Molecular, Cellular and Developmental Neurobiology, 28002 Madrid, Spain Instituto Cajal-CSIC, Department of Molecular, Cellular and Developmental Neurobiology, 28002 Madrid, Spain Instituto Cajal-CSIC, Department of Molecular, Cellular and Developmental Neurobiology, 28002 Madrid, Spain The mammalian central nervous system (CNS) exhibits limited regenerative capacity and the mechanisms that mediate its regeneration are not fully understood. Here, we present a novel experimental design to damage the CNS by using a contusion injury paradigm. The design of this protocol allows the study of long-term and short-term cellular responses, including those of the CNS and the immune system, and of any implications regarding functional recovery. We demonstrate for the first time that adult Drosophila melanogaster glial cells undergo spontaneous functional recovery following crush injury. This crush injury leads to an intermediate level of functional recovery after damage, which is ideal to screen for genes that facilitate or prevent the regeneration process. Here, we validate this model and analyse the immune responses of glial cells as a central regulator of functional regeneration. Additionally, we demonstrate that glial cells and macrophages contribute to functional regeneration through mechanisms involving the Jun N-terminal kinase (JNK) pathway and the Drosophila protein Draper (Drpr), characteristic of other neural injury paradigms. We show that macrophages are recruited to the injury site and are required for functional recovery. Further, we show that the proteins Grindelwald and Drpr in Drosophila glial cells mediate activation of JNK, and that expression of drpr is dependent on JNK activation. Finally, we link neuron-glial communication and the requirement of neuronal vesicular transport to regulation of the JNK pathway and functional recovery. This article has an associated First Person interview with the first author of the paper.http://dmm.biologists.org/content/14/5/dmm044669jnkmacrophagescns damagegliaimmune responseregeneration
collection DOAJ
language English
format Article
sources DOAJ
author María Losada-Pérez
Nuria García-Guillén
Sergio Casas-Tintó
spellingShingle María Losada-Pérez
Nuria García-Guillén
Sergio Casas-Tintó
A novel injury paradigm in the central nervous system of adult Drosophila: molecular, cellular and functional aspects
Disease Models & Mechanisms
jnk
macrophages
cns damage
glia
immune response
regeneration
author_facet María Losada-Pérez
Nuria García-Guillén
Sergio Casas-Tintó
author_sort María Losada-Pérez
title A novel injury paradigm in the central nervous system of adult Drosophila: molecular, cellular and functional aspects
title_short A novel injury paradigm in the central nervous system of adult Drosophila: molecular, cellular and functional aspects
title_full A novel injury paradigm in the central nervous system of adult Drosophila: molecular, cellular and functional aspects
title_fullStr A novel injury paradigm in the central nervous system of adult Drosophila: molecular, cellular and functional aspects
title_full_unstemmed A novel injury paradigm in the central nervous system of adult Drosophila: molecular, cellular and functional aspects
title_sort novel injury paradigm in the central nervous system of adult drosophila: molecular, cellular and functional aspects
publisher The Company of Biologists
series Disease Models & Mechanisms
issn 1754-8403
1754-8411
publishDate 2021-05-01
description The mammalian central nervous system (CNS) exhibits limited regenerative capacity and the mechanisms that mediate its regeneration are not fully understood. Here, we present a novel experimental design to damage the CNS by using a contusion injury paradigm. The design of this protocol allows the study of long-term and short-term cellular responses, including those of the CNS and the immune system, and of any implications regarding functional recovery. We demonstrate for the first time that adult Drosophila melanogaster glial cells undergo spontaneous functional recovery following crush injury. This crush injury leads to an intermediate level of functional recovery after damage, which is ideal to screen for genes that facilitate or prevent the regeneration process. Here, we validate this model and analyse the immune responses of glial cells as a central regulator of functional regeneration. Additionally, we demonstrate that glial cells and macrophages contribute to functional regeneration through mechanisms involving the Jun N-terminal kinase (JNK) pathway and the Drosophila protein Draper (Drpr), characteristic of other neural injury paradigms. We show that macrophages are recruited to the injury site and are required for functional recovery. Further, we show that the proteins Grindelwald and Drpr in Drosophila glial cells mediate activation of JNK, and that expression of drpr is dependent on JNK activation. Finally, we link neuron-glial communication and the requirement of neuronal vesicular transport to regulation of the JNK pathway and functional recovery. This article has an associated First Person interview with the first author of the paper.
topic jnk
macrophages
cns damage
glia
immune response
regeneration
url http://dmm.biologists.org/content/14/5/dmm044669
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