Origin of wiring specificity in an olfactory map revealed by neuron type-specific, time-lapse imaging of dendrite targeting.

D. melanogaster dendrite targeting developmental biology neural circuit assembly neuronal remodeling neuroscience olfactory system projection neurons time-lapse imaging

Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
28 03 2023
Historique:
received: 11 12 2022
accepted: 27 03 2023
medline: 22 5 2023
pubmed: 29 3 2023
entrez: 28 3 2023
Statut: epublish

Résumé

How does wiring specificity of neural maps emerge during development? Formation of the adult The brain’s ability to sense, act and remember relies on the intricate network of connections between neurons. Organization of these connections into neural maps is critical for processing sensory information. For instance, different odors are represented by specific neurons in a part of the brain known as the olfactory bulb, allowing animals to distinguish between smells. Projection neurons in the olfactory bulb have extensions known as dendrites that receive signals from sensory neurons. Scientists have extensively used the olfactory map in adult fruit flies to study brain wiring because of the specific connections between their sensory and projection neurons. This has led to the discovery of similar wiring strategies in mammals. But how the olfactory map is formed during development is not fully understood. To investigate, Wong et al. built genetic tools to label specific types of olfactory projection neurons during the pupal stage of fruit fly development. This showed that a group of projection neurons directed their dendrites in a clockwise rotation pattern depending on the order in which they were born: the first-born neuron sent dendrites towards the top right of the antennal lobe (the fruit fly equivalent of the olfactory bulb), while the last-born sent dendrites towards the top left. Wong et al. also carried out high-resolution time-lapse imaging of live brains grown in the laboratory to determine how dendrites make wiring decisions. This revealed that projection neurons send dendrites in all directions, but preferentially stabilize those that extend in the direction which the neurons eventually target. Also, live imaging showed neurons could remove old dendrites (used in the larvae) and build new ones (to be used in the adult) simultaneously, allowing them to quickly create new circuits. These experiments demonstrate the value of imaging specific types of neurons to understand the mechanisms that assemble neural maps in the developing brain. Further work could use the genetic tools created by Wong et al. to study how wiring decisions are determined in this and other neural maps by specific genes, potentially yielding insights into neurological disorders associated with wiring defects.

Autres résumés

Type: plain-language-summary (eng)
The brain’s ability to sense, act and remember relies on the intricate network of connections between neurons. Organization of these connections into neural maps is critical for processing sensory information. For instance, different odors are represented by specific neurons in a part of the brain known as the olfactory bulb, allowing animals to distinguish between smells. Projection neurons in the olfactory bulb have extensions known as dendrites that receive signals from sensory neurons. Scientists have extensively used the olfactory map in adult fruit flies to study brain wiring because of the specific connections between their sensory and projection neurons. This has led to the discovery of similar wiring strategies in mammals. But how the olfactory map is formed during development is not fully understood. To investigate, Wong et al. built genetic tools to label specific types of olfactory projection neurons during the pupal stage of fruit fly development. This showed that a group of projection neurons directed their dendrites in a clockwise rotation pattern depending on the order in which they were born: the first-born neuron sent dendrites towards the top right of the antennal lobe (the fruit fly equivalent of the olfactory bulb), while the last-born sent dendrites towards the top left. Wong et al. also carried out high-resolution time-lapse imaging of live brains grown in the laboratory to determine how dendrites make wiring decisions. This revealed that projection neurons send dendrites in all directions, but preferentially stabilize those that extend in the direction which the neurons eventually target. Also, live imaging showed neurons could remove old dendrites (used in the larvae) and build new ones (to be used in the adult) simultaneously, allowing them to quickly create new circuits. These experiments demonstrate the value of imaging specific types of neurons to understand the mechanisms that assemble neural maps in the developing brain. Further work could use the genetic tools created by Wong et al. to study how wiring decisions are determined in this and other neural maps by specific genes, potentially yielding insights into neurological disorders associated with wiring defects.

Identifiants

pubmed: 36975203
doi: 10.7554/eLife.85521
pii: 85521
pmc: PMC10195080
doi:
pii:

Substances chimiques

Drosophila Proteins 0

Banques de données

GEO
['GSE161228']

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDCD NIH HHS
ID : R01 DC005982
Pays : United States

Informations de copyright

© 2023, Wong et al.

Déclaration de conflit d'intérêts

KW, TL, TF, GL, CL, SK, QX, DL, SU, EB, LL No competing interests declared

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Auteurs

Kenneth Kin Lam Wong (KKL)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.

Tongchao Li (T)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.

Tian-Ming Fu (TM)

Howard Hughes Medical Institute, Janelia Research Campus, Ashburn, United States.

Gaoxiang Liu (G)

Advanced Bioimaging Center, Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.

Cheng Lyu (C)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.

Sayeh Kohani (S)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.

Qijing Xie (Q)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.

David J Luginbuhl (DJ)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.

Srigokul Upadhyayula (S)

Advanced Bioimaging Center, Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, United States.
Chan Zuckerberg Biohub, San Francisco, United States.

Eric Betzig (E)

Howard Hughes Medical Institute, Janelia Research Campus, Ashburn, United States.
Advanced Bioimaging Center, Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.
Departments of Molecular and Cell Biology and Physics, Howard Hughes Medical Institute, Helen Wills Neuroscience Institute, University of California, Berkeley, United States.

Liqun Luo (L)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, United States.

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