Evidence map›Paper›PMID 28362388›Full record

ArticleJournal of visualized experiments : JoVE2017

Analyzing Dendritic Morphology in Columns and Layers.

Chun-Yuan Ting, Philip G McQueen, Nishith Pandya, Evan S McCreedy, Matthew McAuliffe, Chi-Hon Lee

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Chun-Yuan TingSection on Neuronal Connectivity, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health (NIH).
Philip G McQueenMathematical and Statistical Computing Laboratory, Center for Information Technology, National Institutes of Health (NIH).
Nishith PandyaBiomedical Imaging Research Services Section, Center for Information Technology, National Institutes of Health (NIH).
Evan S McCreedyBiomedical Imaging Research Services Section, Center for Information Technology, National Institutes of Health (NIH).
Matthew McAuliffeBiomedical Imaging Research Services Section, Center for Information Technology, National Institutes of Health (NIH).
Chi-Hon LeeSection on Neuronal Connectivity, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health (NIH); leechih@mail.nih.gov.

Funding

Scientific Applications Services SectionZIACT000272 · CIT · CENTER FOR INFORMATION TECHNOLOGY · PI MCAULIFFE, MATTHEW · 2009 to 2021
$9.9M
Genetic dissection of color-vision circuitsZIAHD008776 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI LEE, CHI-HON · 2009 to 2018
$7.2M
Dendrite Development of Medulla Tm NeuronsZIAHD008913 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI LEE, CHI-HON · 2011 to 2018
$4.0M
Physical modeling of biological systemsZIACT000276 · CIT · CENTER FOR INFORMATION TECHNOLOGY · PI MCQUEEN, PHILIP · 2013 to 2020
$1.5M
6 · The paper itself

Abstract

In many regions of the central nervous systems, such as the fly optic lobes and the vertebrate cortex, synaptic circuits are organized in layers and columns to facilitate brain wiring during development and information processing in developed animals. Postsynaptic neurons elaborate dendrites in type-specific patterns in specific layers to synapse with appropriate presynaptic terminals. The fly medulla neuropil is composed of 10 layers and about 750 columns; each column is innervated by dendrites of over 38 types of medulla neurons, which match with the axonal terminals of some 7 types of afferents in a type-specific fashion. This report details the procedures to image and analyze dendrites of medulla neurons. The workflow includes three sections: (i) the dual-view imaging section combines two confocal image stacks collected at orthogonal orientations into a high-resolution 3D image of dendrites; (ii) the dendrite tracing and registration section traces dendritic arbors in 3D and registers dendritic traces to the reference column array; (iii) the dendritic analysis section analyzes dendritic patterns with respect to columns and layers, including layer-specific termination and planar projection direction of dendritic arbors, and derives estimates of dendritic branching and termination frequencies. The protocols utilize custom plugins built on the open-source MIPAV (Medical Imaging Processing, Analysis, and Visualization) platform and custom toolboxes in the matrix laboratory language. Together, these protocols provide a complete workflow to analyze the dendritic routing of Drosophila medulla neurons in layers and columns, to identify cell types, and to determine defects in mutants.

Indexed as

AnimalsDendritic CellsDrosophilaModels, AnimalNeuronsPresynaptic TerminalsSynapses

Identifiers

PMID28362388
PMCPMC5408983

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.