Evidence map›Paper›PMID 27413766›Full record

ArticleNeurophotonics2016

Superresolving dendritic spine morphology with STED microscopy under holographic photostimulation.

Marcel Andreas Lauterbach, Marc Guillon, Claire Desnos, Dany Khamsing, Zahra Jaffal, François Darchen, Valentina Emiliani

Open access · hybridAbstract read
In one paragraph

Article in Neurophotonics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
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

7 authors at 4 institutions in 1 country.

Marcel Andreas LauterbachUniversity Paris Descartes , Wavefront-Engineering Microscopy Group, Neurophotonics Laboratory, CNRS UMR8250, Sorbonne Paris Cité, 45, rue des Saints Pères, Paris 75006, France.
Marc GuillonUniversity Paris Descartes , Wavefront-Engineering Microscopy Group, Neurophotonics Laboratory, CNRS UMR8250, Sorbonne Paris Cité, 45, rue des Saints Pères, Paris 75006, France.
Claire DesnosUniversity Paris Descartes , Synapic Trafficking Group, Neurophotonics Laboratory, CNRS UMR8250, Sorbonne Paris Cité, 45, rue des Saints Pères, Paris 75006, France.
Dany KhamsingUniversity Paris Descartes , Synapic Trafficking Group, Neurophotonics Laboratory, CNRS UMR8250, Sorbonne Paris Cité, 45, rue des Saints Pères, Paris 75006, France.
Zahra JaffalUniversity Paris Descartes , Synapic Trafficking Group, Neurophotonics Laboratory, CNRS UMR8250, Sorbonne Paris Cité, 45, rue des Saints Pères, Paris 75006, France.
François DarchenUniversity Paris Descartes , Synapic Trafficking Group, Neurophotonics Laboratory, CNRS UMR8250, Sorbonne Paris Cité, 45, rue des Saints Pères, Paris 75006, France.
Valentina EmilianiUniversity Paris Descartes , Wavefront-Engineering Microscopy Group, Neurophotonics Laboratory, CNRS UMR8250, Sorbonne Paris Cité, 45, rue des Saints Pères, Paris 75006, France.
Sorbonne Paris Cité · FRCentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging all-optical methods provide unique possibilities for noninvasive studies of physiological processes at the cellular and subcellular scale. On the one hand, superresolution microscopy enables observation of living samples with nanometer resolution. On the other hand, light can be used to stimulate cells due to the advent of optogenetics and photolyzable neurotransmitters. To exploit the full potential of optical stimulation, light must be delivered to specific cells or even parts of cells such as dendritic spines. This can be achieved with computer generated holography (CGH), which shapes light to arbitrary patterns by phase-only modulation. We demonstrate here in detail how CGH can be incorporated into a stimulated emission depletion (STED) microscope for photostimulation of neurons and monitoring of nanoscale morphological changes. We implement an original optical system to allow simultaneous holographic photostimulation and superresolution STED imaging. We present how synapses can be clearly visualized in live cells using membrane stains either with lipophilic organic dyes or with fluorescent proteins. We demonstrate the capabilities of this microscope to precisely monitor morphological changes of dendritic spines after stimulation. These all-optical methods for cell stimulation and monitoring are expected to spread to various fields of biological research in neuroscience and beyond.

Indexed as

computer generated holographyholographyphotostimulationplasticityspine morphologySTEDSTED microscopyuncaging

Identifiers

PMID27413766
PMCPMC4916265
OpenAlexW2465725572

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.