Evidence map›Paper›PMID 25772507›Full record

ArticleBrain structure & function2016

Simplified CLARITY for visualizing immunofluorescence labeling in the developing rat brain.

Huiyuan Zheng, Linda Rinaman

Abstract read
In one paragraph

Article in Brain structure & function, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
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  5. A diffusion MRI-based spatiotemporal continuum of the embryonic mouse brain for probing gene-neuroanatomy connections.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  15. Advances in CLARITY-based tissue clearing and imaging.Experimental and therapeutic medicine · 2018
    Review
  16. Article
  17. Review
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  19. Article
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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

2 authors.

Huiyuan ZhengDepartment of Neuroscience, University of Pittsburgh, A210 Langley Hall, Pittsburgh, PA, 15260, USA.
Linda RinamanDepartment of Neuroscience, University of Pittsburgh, A210 Langley Hall, Pittsburgh, PA, 15260, USA. rinaman@pitt.edu.

Funding

POSTNATAL DEVELOPMENT OF VAGAL-HYPOTHALAMIC CONNECTIONSR01MH059911 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RINAMAN, LINDA M · 1999 to 2024
$7.3M
Brainstem Satiety Circuits and High Fat Diet HyperphagiaR01DK100685 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RINAMAN, LINDA M · 2014 to 2018
$1.6M
Early Life Experience Shapes Visceral CircuitsR01MH081817 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RINAMAN, LINDA M · 2009 to 2013
$1.6M
NIDDK NIH HHS R01 DK100685NIMH NIH HHS R01 MH059911NIMH NIH HHS R01 MH081817
6 · The paper itself

Abstract

CLARITY is an innovative technological advance in which intact biological tissue is transformed into a "nanoporous hydrogel-hybridized form" (Chung et al. 2013; Chung and Deisseroth 2013) with markedly improved chemical and optical accessibility, permitting fluorescent visualization and extraction of high-resolution structural data from mm-thick blocks of tissue. CLARITY affords an excellent but as yet unexploited opportunity to visualize the growth and maturation of phenotypically identified neurons and axonal processes in the developing brain. This brief report describes a moderately revised, simplified, and less expensive CLARITY protocol that effectively reveals the structure of chemically identified neurons in whole neonatal/juvenile rat brains and tissue slabs. Rats [postnatal day (P)0-24] were transcardially perfused with one of two fixative/hydrogel solutions, followed by hydrogel polymerization to generate brain hybrids. Whole brain hybrids or 2.0-mm-thick coronal slabs were passively cleared of lipid and then processed for dual immunofluorescence labeling, including labeling using tyramide signal amplification. After refractive index matching using 2,20-Thiodiethanol (60 % solution), a Leica confocal microscope equipped with a CLARITY objective was used to view the hypothalamus in whole brain hybrids or slabs. Collected image stacks revealed the distribution and three-dimensional structure of hypothalamic pro-oxyphysin (oxytocin)-, neuropeptide Y-, glucagon-like peptide-1-, and tyrosine hydroxylase-immunopositive neurons and processes within large tissue volumes. Outstanding structural preservation and immunolabeling quality demonstrates the efficacy of this approach for interrogating chemically defined neural circuits as they develop in postnatal rodent brain.

Indexed as

AnimalsBrainFemaleFluorescent Antibody TechniqueHistological TechniquesMaleMicroscopy, ConfocalNeuronsRatsRats, Sprague-DawleyRefractometryCLARITYImmunofluorescenceNeonatal

Identifiers

PMID25772507
PMCPMC4569540

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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.