Evidence map›Paper›PMID 28966653›Full record

ArticleNeural regeneration research2017

A novel triple immunoenzyme staining enables simultaneous identification of all muscle fiber types on a single skeletal muscle cryosection from normal, denervated or reinnervated rats.

Peng Wu, Shuya Zhang, Robert J Spinner, Michael Torres Lizardi, Yudong Gu, Cong Yu, Michael J Yaszemski, Anthony J Windebank, Huan Wang

Open access · goldAbstract read
In one paragraph

Article in Neural regeneration research, 2017. 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
0.2field-weighted citation impact, top 44% 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

0 citing papers in PubMed, 3 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

9 authors at 6 institutions in 2 countries.

Peng WuDepartment of Neurological Surgery, Mayo Clinic, Rochester, MN, USA.
Shuya ZhangDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Robert J SpinnerDepartment of Neurological Surgery, Mayo Clinic, Rochester, MN, USA.
Michael Torres LizardiDepartment of Medicine, New York Presbyterian Weill Cornell Medical Center, New York, NY, USA.
Yudong GuDepartment of Hand Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Cong YuDepartment of Hand Surgery, Huashan Hospital, Fudan University, Shanghai, China.
Michael J YaszemskiDepartment of Orthopedic Surgery and Biomedical Engineering, Mayo Clinic, Rochester, MN, USA.
Anthony J WindebankDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Huan WangDepartment of Neurological Surgery, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0002-5540-0648
Mayo Clinic in Arizona · USHuashan Hospital · CNCornell University · USFudan University · CNMayo Clinic · USNeurological Surgery · US

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
Mayo Clinic Center for Translational Science ActivitiesTL1TR000137 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$2.1M
NCATS NIH HHS TL1 TR000137NCATS NIH HHS UL1 TR000135
6 · The paper itself

Abstract

Triple immunofluorescence staining has recently been developed to simultaneously identify all muscle fibers on a single cryosection which is helpful for clinical and basic research, but it has disadvantages such as fast photobleaching and unclear outlines of muscle fibers. Triple immunoenzyme staining (TIE) is likely to avoid these disadvantages. In this study, we aimed to establish a sensitive and specific TIE technique to identify fiber types in normal, denervated, and reinnervated rat muscles, and to develop a systematic sampling method for muscle fiber quantification. Tibialis anterior and soleus from normal, denervated, and reinnervated Lewis rat hind limbs were used. Five consecutive cryosections were cut from each muscle, including one for TIE and four for single immunoenzyme staining (SIE). The TIE was performed using the polymerized reporter enzyme staining system for the first two antigens (A4.74 for MyHC-IIA, BA-F8 for MyHC-I) and alkaline phosphatase staining system for the third antigen (BF-F3 for MyHC-IIB), followed by corresponding detective systems and respective chromogens. The type of muscle fibers was quantified by systematic sampling at 12.5%, 25%, 33% and 50% of all muscle fibers, and was compared with that acquired from counting all the fibers (100%). All muscle fiber phenotypes, including pure and hybrid, could be simultaneously identified on a single TIE cryosection with clear outlines. The fiber types on TIE slides matched well with their respective counterpart on the consecutive SIE slides with a 95% match rate. Systematic sampling of 12.5% fibers could represent the true fiber type distribution of the entire muscle section. Our results suggest that novel TIE can effectively visualize fiber types in normal, denervated or reinnervated rat muscles.

Indexed as

immunohistochemistrymuscle fiber phenotypingmyosin heavy chainnerve regenerationneural regenerationratstriple immunoenzyme staining

Identifiers

PMID28966653
PMCPMC5607833
OpenAlexW2748002913

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.