Evidence map›Paper›PMID 25915122›Full record

ArticleNature methods2015

Multispectral labeling technique to map many neighboring axonal projections in the same tissue.

Shlomo Tsuriel, Sagi Gudes, Ryan W Draft, Alexander M Binshtok, Jeff W Lichtman

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Nature methods, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.8field-weighted citation impact, top 5% of its field
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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  7. Article
  8. Multispectral Live-Cell Imaging.Current protocols in cell biology · 2018
    Article
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  10. Review
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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

5 authors at 2 institutions in 2 countries.

Shlomo Tsuriel1] Center for Brain Science, Harvard University, Cambridge, Massachusetts, USA. [2] Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts, USA. [3] Department of Medical Neurobiology, Institute for Medical Research Israel Canada Faculty of Medicine, The Hebrew University, Jerusalem, Israel. [4] The Edmond and Lily Safra Center for Brain Sciences, The Hebrew University, Jerusalem, Israel.
Sagi Gudes1] Department of Medical Neurobiology, Institute for Medical Research Israel Canada Faculty of Medicine, The Hebrew University, Jerusalem, Israel. [2] The Edmond and Lily Safra Center for Brain Sciences, The Hebrew University, Jerusalem, Israel.
Ryan W Draft1] Center for Brain Science, Harvard University, Cambridge, Massachusetts, USA. [2] Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts, USA.
Alexander M Binshtok1] Department of Medical Neurobiology, Institute for Medical Research Israel Canada Faculty of Medicine, The Hebrew University, Jerusalem, Israel. [2] The Edmond and Lily Safra Center for Brain Sciences, The Hebrew University, Jerusalem, Israel.
Jeff W Lichtman1] Center for Brain Science, Harvard University, Cambridge, Massachusetts, USA. [2] Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts, USA.
Harvard University · USHebrew University of Jerusalem · IL

Funding

Res Support CoreP50MH094271 · NIMH · HARVARD UNIVERSITY · PI HENSCH, TAKAO K · 2011 to 2022
$18.6M
NIMH NIH HHS P50 MH094271
6 · The paper itself

Abstract

We describe a method to map the location of axonal arbors of many individual neurons simultaneously via the spectral properties of retrogradely transported dye-labeled vesicles. We inject overlapping regions of an axon target area with three or more different colored retrograde tracers. On the basis of the combinations and intensities of the colors in the individual vesicles transported to neuronal somata, we calculate the projection sites of each neuron's axon. This neuronal positioning system (NPS) enables mapping of many axons in a simple automated way. In our experiments, NPS combined with spectral (Brainbow) labeling of the input to autonomic ganglion cells showed that the locations of ganglion cell projections to a mouse salivary gland related to the identities of their preganglionic axonal innervation. NPS could also delineate projections of many axons simultaneously in the mouse central nervous system.

Indexed as

AxonsAnimalsBrain MappingCerebral CortexComputer GraphicsGanglia, ParasympatheticImage Processing, Computer-AssistedMiceNeural PathwaysNeuronsStaining and LabelingThalamus

Identifiers

PMID25915122
OpenAlexW2054671370

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.