Evidence map›Paper›PMID 36995613›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Tissue Clearing and Confocal Microscopic Imaging for Skeletal Muscle.

Smrithi Karthikeyan, Yoko Asakura, Mayank Verma, Atsushi Asakura

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. 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
3.3field-weighted citation impact, top 8% 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, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Imaging analysis for muscle stem cells and regeneration.Frontiers in cell and developmental biology · 2024
    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

4 authors at 1 institution in 1 country.

Smrithi KarthikeyanStem Cell Institute, University of Minnesota Medical School, Minneapolis, MN, USA.
Yoko AsakuraStem Cell Institute, University of Minnesota Medical School, Minneapolis, MN, USA.
Mayank VermaStem Cell Institute, University of Minnesota Medical School, Minneapolis, MN, USA.
Atsushi AsakuraStem Cell Institute, University of Minnesota Medical School, Minneapolis, MN, USA. asakura@umn.edu.
University of Minnesota · US

Funding

Genetically Engineered Muscle Stem Cell Transplantation for Muscular Dystrophy...R01AR062142 · NIAMS · UNIVERSITY OF MINNESOTA · PI ASAKURA, ATSUSHI · 2012 to 2016
$1.6M
Systemic delivery of muscle stem cell for muscle disease therapyR21AR079033 · NIAMS · UNIVERSITY OF MINNESOTA · PI ASAKURA, ATSUSHI · 2022 to 2023
$375k
Engineering iPSC-Derived Skeletal Muscle and Cells for TransplantationR21AR070319 · NIAMS · UNIVERSITY OF MINNESOTA · PI ASAKURA, ATSUSHI · 2016 to 2017
$372k
NIAMS NIH HHS R01 AR062142NIAMS NIH HHS R21 AR070319NIAMS NIH HHS R21 AR079033
6 · The paper itself

Abstract

Skeletal muscle is a highly ordered tissue composed of a complex network of a diverse variety of cells. The dynamic spatial and temporal interaction between these cells during homeostasis and during times of injury gives the skeletal muscle its regenerative capacity. To properly understand the process of regeneration, a three-dimensional (3-D) imaging process must be conducted. With the advancement of imaging and computing technology, it has become powerful to analyze spatial data from confocal microscope images. In order to prepare whole tissue skeletal muscle samples for confocal imaging, the muscle must be subjected to tissue clearing. With the use of an ideal optical clearing protocol - one that minimizes light scattering via refractive index mismatching - a more accurate 3-D image of the muscle can be produced as it does not involve the physical sectioning of the muscle. While there have been several protocols relating to the study of 3-D biology in whole tissue, these protocols have primarily been focused on the nervous system. In this chapter, we present a new method for skeletal muscle tissue clearing. In addition, this protocol aims to outline the specific parameters required for taking 3-D images of immunofluorescence-stained skeletal muscle samples using a confocal microscope.

Indexed as

Imaging, Three-DimensionalMuscle, SkeletalFluorescent Antibody TechniqueMicroscopy, Confocal3D imagingAngiogenesisEndothelial cellMuscle regenerationMuscle stem cellMuscular dystrophyMyogenesisSatellite cellSkeletal muscleTissue clearing

Identifiers

PMID36995613
OpenAlexW4361305490

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.