Evidence map›Paper›PMID 25453108›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Label-free imaging of Schwann cell myelination by third harmonic generation microscopy.

Hyungsik Lim, Denis Sharoukhov, Imran Kassim, Yanqing Zhang, James L Salzer, Carmen V Melendez-Vasquez

Abstract readEvaluation Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

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  12. A near-infrared AIE fluorescent probe for myelin imaging: From sciatic nerve to the optically cleared brain tissue in 3D.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Review
  14. Article
  15. Label-Free Multiphoton Microscopy: Much More Than Fancy Images.International journal of molecular sciences · 2021
    Review
  16. Article
  17. 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

6 authors.

Hyungsik LimDepartments of Physics and hyungsik.lim@hunter.cuny.edu.
Denis SharoukhovDepartments of Physics and.
Imran KassimBiology, Hunter College of the City University of New York, New York, NY 10065; and.
Yanqing ZhangDepartment of Cell Biology and Neurology, New York University School of Medicine, NY 11203.
James L SalzerDepartment of Cell Biology and Neurology, New York University School of Medicine, NY 11203.
Carmen V Melendez-VasquezBiology, Hunter College of the City University of New York, New York, NY 10065; and.

Funding

Basic and Translational Research Center for Reducing Health DisparitiesG12MD007599 · NIMHD · HUNTER COLLEGE · PI ANGULO, JESUS A · 2012 to 2017
$14.6M
Node of Ranvier Assembly: Role of Axo-Glial InteractionsR01NS043474 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SALZER, JAMES · 2002 to 2024
$7.9M
Regulation of Schwann cell ensheathment and myelination by type III Neuregulin 1R01NS026001 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SALZER, JAMES · 1988 to 2016
$6.5M
Regulation of myelination by myosin II-mediated mechanotransductionSC1NS000001 · NINDS · HUNTER COLLEGE · PI MELENDEZ-VASQUEZ, CARMEN V · 2013 to 2016
$1.4M
Visualization of In Vivo Myelin Architecture Using Nonlinear MicroscopySC2GM096884 · NIGMS · HUNTER COLLEGE · PI LIM, HYUNGSIK · 2012 to 2014
$454k
NIGMS NIH HHS GM096884NIGMS NIH HHS SC2 GM096884NIMHD NIH HHS G12 MD007599NIMHD NIH HHS MD007599NINDS NIH HHS NS000001NINDS NIH HHS NS26001NINDS NIH HHS R01 NS026001NINDS NIH HHS R01 NS043474NINDS NIH HHS SC1 NS000001
6 · The paper itself

Abstract

Understanding the dynamic axon-glial cell interaction underlying myelination is hampered by the lack of suitable imaging techniques. Here we demonstrate third harmonic generation microscopy (THGM) for label-free imaging of myelinating Schwann cells in live culture and ex vivo and in vivo tissue. A 3D structure was acquired for a variety of compact and noncompact myelin domains, including juxtaparanodes, Schmidt-Lanterman incisures, and Cajal bands. Other subcellular features of Schwann cells that escape traditional optical microscopies were also visualized. We tested THGM for morphometry of compact myelin. Unlike current methods based on electron microscopy, g-ratio could be determined along an extended length of myelinated fiber in the physiological condition. The precision of THGM-based g-ratio estimation was corroborated in mouse models of hypomyelination. Finally, we demonstrated the feasibility of THGM to monitor morphological changes of myelin during postnatal development and degeneration. The outstanding capabilities of THGM may be useful for elucidation of the mechanism of myelin formation and pathogenesis.

Indexed as

AnimalsDemyelinating DiseasesImaging, Three-DimensionalLasersMiceMicroscopyMicroscopy, Fluorescence, MultiphotonMyelin SheathRatsSchwann Cellslabel-free imagingmorphometrymultiphoton microscopymyelinSchwann cell

Identifiers

PMID25453108
PMCPMC4273419

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.