Literature DB >> 33758182

Axonal chemokine-like Orion induces astrocyte infiltration and engulfment during mushroom body neuronal remodeling.

Ana Boulanger1, Camille Thinat2, Stephan Züchner3, Lee G Fradkin4, Hugues Lortat-Jacob5, Jean-Maurice Dura6.   

Abstract

The remodeling of neurons is a conserved fundamental mechanism underlying nervous system maturation and function. Astrocytes can clear neuronal debris and they have an active role in neuronal remodeling. Developmental axon pruning of Drosophila memory center neurons occurs via a degenerative process mediated by infiltrating astrocytes. However, how astrocytes are recruited to the axons during brain development is unclear. Using an unbiased screen, we identify the gene requirement of orion, encoding for a chemokine-like protein, in the developing mushroom bodies. Functional analysis shows that Orion is necessary for both axonal pruning and removal of axonal debris. Orion performs its functions extracellularly and bears some features common to chemokines, a family of chemoattractant cytokines. We propose that Orion is a neuronal signal that elicits astrocyte infiltration and astrocyte-driven axonal engulfment required during neuronal remodeling in the Drosophila developing brain.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 33758182     DOI: 10.1038/s41467-021-22054-x

Source DB:  PubMed          Journal:  Nat Commun        ISSN: 2041-1723            Impact factor:   14.919


  46 in total

1.  Axon pruning during Drosophila metamorphosis: evidence for local degeneration and requirement of the ubiquitin-proteasome system.

Authors:  Ryan J Watts; Eric D Hoopfer; Liqun Luo
Journal:  Neuron       Date:  2003-06-19       Impact factor: 17.173

2.  Glia engulf degenerating axons during developmental axon pruning.

Authors:  Ryan J Watts; Oren Schuldiner; John Perrino; Camilla Larsen; Liqun Luo
Journal:  Curr Biol       Date:  2004-04-20       Impact factor: 10.834

3.  Engulfing action of glial cells is required for programmed axon pruning during Drosophila metamorphosis.

Authors:  Takeshi Awasaki; Kei Ito
Journal:  Curr Biol       Date:  2004-04-20       Impact factor: 10.834

Review 4.  Axon retraction and degeneration in development and disease.

Authors:  Liqun Luo; Dennis D M O'Leary
Journal:  Annu Rev Neurosci       Date:  2005       Impact factor: 12.449

Review 5.  Diverse cellular and molecular modes of axon degeneration.

Authors:  Lukas J Neukomm; Marc R Freeman
Journal:  Trends Cell Biol       Date:  2014-04-27       Impact factor: 20.808

Review 6.  Errant gardeners: glial-cell-dependent synaptic pruning and neurodevelopmental disorders.

Authors:  Urte Neniskyte; Cornelius T Gross
Journal:  Nat Rev Neurosci       Date:  2017-09-21       Impact factor: 34.870

Review 7.  Nuclear receptors and Drosophila neuronal remodeling.

Authors:  Ana Boulanger; Jean-Maurice Dura
Journal:  Biochim Biophys Acta       Date:  2014-06-02

Review 8.  Axon and dendrite pruning in Drosophila.

Authors:  Fengwei Yu; Oren Schuldiner
Journal:  Curr Opin Neurobiol       Date:  2014-05-04       Impact factor: 6.627

Review 9.  A fly's view of neuronal remodeling.

Authors:  Shiri P Yaniv; Oren Schuldiner
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2016-06-28       Impact factor: 5.814

Review 10.  Mechanisms of developmental neurite pruning.

Authors:  Oren Schuldiner; Avraham Yaron
Journal:  Cell Mol Life Sci       Date:  2014-09-12       Impact factor: 9.261

View more
  1 in total

Review 1.  Mechanisms governing activity-dependent synaptic pruning in the developing mammalian CNS.

Authors:  Travis E Faust; Georgia Gunner; Dorothy P Schafer
Journal:  Nat Rev Neurosci       Date:  2021-09-20       Impact factor: 38.755

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.