Evidence map›Paper›PMID 39134856›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Measuring Retrograde Actin Flow in Neuronal Growth Cones.

Laura Pulido Cifuentes, Daniel M Suter

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2024. 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

2 authors.

Laura Pulido CifuentesDepartment of Biological Sciences, Purdue University, West Lafayette, IN, USA.
Daniel M SuterDepartment of Biological Sciences, Purdue University, West Lafayette, IN, USA. dsuter@purdue.edu.ORCID 0000-0002-5230-7229

Funding

NADPH oxidase regulates growth cone guidanceR01NS117701 · NINDS · PURDUE UNIVERSITY · PI SUTER, DANIEL MARCEL · 2020 to 2024
$1.8M
NINDS NIH HHS R01 NS117701
6 · The paper itself

Abstract

Actin flow refers to the motion of the F-actin cytoskeleton and has been observed in many different cell types, especially in motile cells including neuronal growth cones. The direction of the actin flow is generally retrograde from the periphery toward the center of the cell. Actin flow can be harnessed for forward movement of the cell through substrate-cytoskeletal coupling; thus, a key function of actin flow is in cell locomotion. In this chapter, we illustrate three different methods of quantifying retrograde F-actin flow in growth cones derived from cultured Aplysia bag cell neurons. These methods include tracking the movement of surface marker beads as well as kymograph analysis of time-lapse sequences acquired by differential interference contrast (DIC) imaging or fluorescent speckle microscopy (FSM). Due to their large size, Aplysia neuronal growth cones are uniquely suited for these methods; however, they can also be applied to any other growth cones with clear F-actin-rich peripheral domains.

Indexed as

ActinsAplysiaGrowth ConesActin CytoskeletonAnimalsCells, CulturedKymographyMicroscopy, FluorescenceNeuronsTime-Lapse ImagingActinsActin cytoskeletonKymographNeuronal growth coneRetrograde F-actin flowTime-lapse imaging

Identifiers

PMID39134856

What OpenQuestion holds

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Registered trials

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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.