Literature DB >> 26367447

Axon ensheathment and metabolic supply by glial cells in Drosophila.

Stefanie Schirmeier1, Till Matzat1, Christian Klämbt2.   

Abstract

Neuronal function requires constant working conditions and a well-balanced supply of ions and metabolites. The metabolic homeostasis in the nervous system crucially depends on the presence of glial cells, which nurture and isolate neuronal cells. Here we review recent findings on how these tasks are performed by glial cells in the genetically amenable model organism Drosophila melanogaster. Despite the small size of its nervous system, which would allow diffusion of metabolites, a surprising division of labor between glial cells and neurons is evident. Glial cells are glycolytically active and transfer lactate and alanine to neurons. Neurons in turn do not require glycolysis but can use the glially provided compounds for their energy homeostasis. Besides feeding neurons, glial cells also insulate neuronal axons in a way similar to Remak fibers in the mammalian nervous system. The molecular mechanisms orchestrating this insulation require neuregulin signaling and resemble the mechanisms controlling glial differentiation in mammals surprisingly well. We hypothesize that metabolic cross talk and insulation of neurons by glial cells emerged early during evolution as two closely interlinked features in the nervous system. This article is part of a Special Issue entitled SI: Myelin Evolution.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Blood–brain barrier; Drosophila nervous system; Glia; Metabolic coupling; Nutrient supply

Mesh:

Year:  2015        PMID: 26367447     DOI: 10.1016/j.brainres.2015.09.003

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  11 in total

1.  Axonal Ensheathment in the Nervous System of Lamprey: Implications for the Evolution of Myelinating Glia.

Authors:  Marie-Theres Weil; Saskia Heibeck; Mareike Töpperwien; Susanne Tom Dieck; Torben Ruhwedel; Tim Salditt; María C Rodicio; Jennifer R Morgan; Klaus-Armin Nave; Wiebke Möbius; Hauke B Werner
Journal:  J Neurosci       Date:  2018-06-25       Impact factor: 6.167

Review 2.  Glial contributions to neuronal health and disease: new insights from Drosophila.

Authors:  Mary A Logan
Journal:  Curr Opin Neurobiol       Date:  2017-11-06       Impact factor: 6.627

3.  Cisplatin induces mitochondrial deficits in Drosophila larval segmental nerve.

Authors:  Jewel L Podratz; Han Lee; Patrizia Knorr; Stephanie Koehler; Steven Forsythe; Kelsey Lambrecht; Suzette Arias; Kiley Schmidt; Gabrielle Steinhoff; Georgiy Yudintsev; Amy Yang; Eugenia Trushina; Anthony Windebank
Journal:  Neurobiol Dis       Date:  2016-10-17       Impact factor: 5.996

4.  The Drosophila Transcription Factor Dimmed Affects Neuronal Growth and Differentiation in Multiple Ways Depending on Neuron Type and Developmental Stage.

Authors:  Yiting Liu; Jiangnan Luo; Dick R Nässel
Journal:  Front Mol Neurosci       Date:  2016-10-13       Impact factor: 5.639

5.  TRAP-seq Profiling and RNAi-Based Genetic Screens Identify Conserved Glial Genes Required for Adult Drosophila Behavior.

Authors:  Fanny S Ng; Sukanya Sengupta; Yanmei Huang; Amy M Yu; Samantha You; Mary A Roberts; Lakshmanan K Iyer; Yongjie Yang; F Rob Jackson
Journal:  Front Mol Neurosci       Date:  2016-12-22       Impact factor: 5.639

6.  Mitochondrial dysfunction induces dendritic loss via eIF2α phosphorylation.

Authors:  Taiichi Tsuyama; Asako Tsubouchi; Tadao Usui; Hiromi Imamura; Tadashi Uemura
Journal:  J Cell Biol       Date:  2017-02-16       Impact factor: 10.539

Review 7.  Macrophages and Their Organ Locations Shape Each Other in Development and Homeostasis - A Drosophila Perspective.

Authors:  Anjeli Mase; Jordan Augsburger; Katja Brückner
Journal:  Front Cell Dev Biol       Date:  2021-03-11

8.  Multifunctional glial support by Semper cells in the Drosophila retina.

Authors:  Mark A Charlton-Perkins; Edward D Sendler; Elke K Buschbeck; Tiffany A Cook
Journal:  PLoS Genet       Date:  2017-05-31       Impact factor: 5.917

9.  The SLC36 transporter Pathetic is required for neural stem cell proliferation and for brain growth under nutrition restriction.

Authors:  Shiyun Feng; Evanthia Zacharioudaki; Kat Millen; Sarah J Bray
Journal:  Neural Dev       Date:  2020-08-02       Impact factor: 3.842

10.  Polyploidy in the adult Drosophila brain.

Authors:  Shyama Nandakumar; Olga Grushko; Laura A Buttitta
Journal:  Elife       Date:  2020-08-25       Impact factor: 8.140

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