Cellular bases of olfactory circuit assembly revealed by systematic time-lapse imaging.

time-lapse imaging, circuit assembly, olfactory system, olfactory receptor neurons, antennal lobe, Drosophilia, growth cone, cytoskeleton, bilateral symmetry, target selection

Journal

Cell
ISSN: 1097-4172
Titre abrégé: Cell
Pays: United States
ID NLM: 0413066

Informations de publication

Date de publication:
30 09 2021
Historique:
received: 23 04 2021
revised: 21 07 2021
accepted: 24 08 2021
pubmed: 23 9 2021
medline: 8 1 2022
entrez: 22 9 2021
Statut: ppublish

Résumé

Neural circuit assembly features simultaneous targeting of numerous neuronal processes from constituent neuron types, yet the dynamics is poorly understood. Here, we use the Drosophila olfactory circuit to investigate dynamic cellular processes by which olfactory receptor neurons (ORNs) target axons precisely to specific glomeruli in the ipsi- and contralateral antennal lobes. Time-lapse imaging of individual axons from 30 ORN types revealed a rich diversity in extension speed, innervation timing, and ipsilateral branch locations and identified that ipsilateral targeting occurs via stabilization of transient interstitial branches. Fast imaging using adaptive optics-corrected lattice light-sheet microscopy showed that upon approaching target, many ORN types exhibiting "exploring branches" consisted of parallel microtubule-based terminal branches emanating from an F-actin-rich hub. Antennal nerve ablations uncovered essential roles for bilateral axons in contralateral target selection and for ORN axons to facilitate dendritic refinement of postsynaptic partner neurons. Altogether, these observations provide cellular bases for wiring specificity establishment.

Identifiants

pubmed: 34551316
pii: S0092-8674(21)01013-8
doi: 10.1016/j.cell.2021.08.030
pmc: PMC8545656
mid: NIHMS1736620
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

5107-5121.e14

Subventions

Organisme : NIDCD NIH HHS
ID : K99 DC018830
Pays : United States
Organisme : NIDCD NIH HHS
ID : R01 DC005982
Pays : United States

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

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Auteurs

Tongchao Li (T)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA. Electronic address: tongchal@stanford.edu.

Tian-Ming Fu (TM)

Howard Hughes Medical Institute, Janelia Research Campus, Ashburn, VA 20417, USA.

Kenneth Kin Lam Wong (KKL)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA.

Hongjie Li (H)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA.

Qijing Xie (Q)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA.

David J Luginbuhl (DJ)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA.

Mark J Wagner (MJ)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA.

Eric Betzig (E)

Howard Hughes Medical Institute, Janelia Research Campus, Ashburn, VA 20417, USA; Departments of Molecular and Cell Biology and Physics, Howard Hughes Medical Institute, Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA 94720, USA; Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Liqun Luo (L)

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA. Electronic address: lluo@stanford.edu.

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