Evidence map›Paper›PMID 36809825›Full record

ArticleJournal of neuroscience methods2023

Simultaneous 3D cellular positioning and apical dendritic morphology of transgenic fluorescent mouse CA3 hippocampal pyramidal neurons.

Christopher J Handwerk, Katherine M Bland, Collin J Denzler, Anna R Kalinowski, Cooper A Brett, Brian D Swinehart, Hilda V Rodriguez, Hollyn N Cook, Elizabeth C Vinson, Madison E Florenz and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroscience methods, 2023. 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
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0citing papers in PubMed
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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, 0 citations in OpenAlex.

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

11 authors at 1 institution in 1 country.

Christopher J HandwerkDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America.
Katherine M BlandDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America.
Collin J DenzlerDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America.
Anna R KalinowskiDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America.
Cooper A BrettDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America.
Brian D SwinehartDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America.
Hilda V RodriguezDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America.
Hollyn N CookDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America.
Elizabeth C VinsonDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America.
Madison E FlorenzDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America.
George S VidalDepartment of Biology, James Madison University, MSC 7801, Harrisonburg, VA 22807, United States of America. Electronic address: vidalgx@jmu.edu.
James Madison University · US

Funding

Integrin Functions in Shaping Cortical CircuitsK01NS107723 · NINDS · JAMES MADISON UNIVERSITY · PI VIDAL, GEORGE · 2020 to 2024
$1.1M
NINDS NIH HHS K01 NS107723
6 · The paper itself

Abstract

backgroundPyramidal neurons throughout hippocampal CA3 are diverse in their dendritic morphology, and CA3 is not homogenous in its structure or function. Nonetheless, few structural studies have captured the precise 3D somatic position and the 3D dendritic morphology of CA3 pyramidal neurons simultaneously. NEW

methodHere, we present a simple approach to reconstruct the apical dendritic morphology of CA3 pyramidal neurons using the transgenic fluorescent Thy1-GFP-M line. The approach simultaneously tracks the dorsoventral, tangential, and radial positions of reconstructed neurons within the hippocampus. It is especially designed for use with transgenic fluorescent mouse lines, which are commonly used in genetic studies of neuronal morphology and development.

resultsWe demonstrate how topographic and morphological data are captured from transgenic fluorescent mouse CA3 pyramidal neurons. COMPARISON WITH EXISTING

methodsThere is no need to select and label CA3 pyramidal neurons with the transgenic fluorescent Thy1-GFP-M line. By taking transverse (not coronal) serial sections, we preserve fine dorsoventral, tangential, and radial somatic positioning of 3D-reconstructed neurons. Because CA2 is well defined by PCP4 immunohistochemistry, we use that technique here to to increase precision in defining tangential position along CA3.

conclusionsWe developed a method for simultaneously collecting precise somatic positioning as well as 3D morphological data among transgenic fluorescent mouse hippocampal pyramidal neurons. This fluorescent method should be compatible with many other transgenic fluorescent reporter lines and immunohistochemical methods, facilitating the capture of topographic and morphological data from a wide variety of genetic experiments in mouse hippocampus.

Indexed as

DendritesPyramidal CellsAnimalsColoring AgentsHippocampusMiceMice, TransgenicNeuronsColoring AgentsCA3Dendritic complexityDendritic morphologyGFP-MPyramidal neuronReconstruction

Identifiers

PMID36809825
PMCPMC10006342
OpenAlexW4321349170

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.