Evidence map›Paper›PMID 37063787›Full record

ArticleChemical science2023

Multimodal high-resolution nano-DESI MSI and immunofluorescence imaging reveal molecular signatures of skeletal muscle fiber types.

Daisy Unsihuay, Hang Hu, Jiamin Qiu, Alessandra Latorre-Palomino, Manxi Yang, Feng Yue, Ruichuan Yin, Shihuan Kuang, Julia Laskin

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

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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

9 authors at 2 institutions in 2 countries.

Daisy UnsihuayDepartment of Chemistry, Purdue University West Lafayette IN 47907 USA jlaskin@purdue.edu.ORCID https://orcid.org/0000-0003-1638-3301
Hang HuDepartment of Chemistry, Purdue University West Lafayette IN 47907 USA jlaskin@purdue.edu.ORCID https://orcid.org/0000-0002-8590-9787
Jiamin QiuDepartment of Animal Sciences, Purdue University West Lafayette IN 47907 USA.
Alessandra Latorre-PalominoDepartment of Chemistry, Universidad Nacional Mayor de San Marcos Lima Peru.ORCID https://orcid.org/0000-0003-4597-0994
Manxi YangDepartment of Chemistry, Purdue University West Lafayette IN 47907 USA jlaskin@purdue.edu.
Feng YueDepartment of Animal Sciences, Purdue University West Lafayette IN 47907 USA.
Ruichuan YinDepartment of Chemistry, Purdue University West Lafayette IN 47907 USA jlaskin@purdue.edu.
Shihuan KuangDepartment of Animal Sciences, Purdue University West Lafayette IN 47907 USA.
Julia LaskinDepartment of Chemistry, Purdue University West Lafayette IN 47907 USA jlaskin@purdue.edu.ORCID https://orcid.org/0000-0002-4533-9644
Purdue University West Lafayette · USNational University of San Marcos · PE

Funding

Metabolic regulation of muscle satellite cell homeostasisR01DK132819 · NIDDK · PURDUE UNIVERSITY · PI Shihuan Kuang · 2023 to 2026
$2.0M
NIDDK NIH HHS R01 DK132819
6 · The paper itself

Abstract

The skeletal muscle is a highly heterogeneous tissue comprised of different fiber types with varying contractile and metabolic properties. The complexity in the analysis of skeletal muscle fibers associated with their small size (30-50 μm) and mosaic-like distribution across the tissue tnecessitates the use of high-resolution imaging to differentiate between fiber types. Herein, we use a multimodal approach to characterize the chemical composition of skeletal fibers in a limb muscle, the gastrocnemius. Specifically, we combine high-resolution nanospray desorption electrospray ionization (nano-DESI) mass spectrometry imaging (MSI) with immunofluorescence (IF)-based fiber type identification. Computational image registration and segmentation approaches are used to integrate the information obtained with both techniques. Our results indicate that the transition between oxidative and glycolytic fibers is associated with shallow chemical gradients (<2.5 fold change in signals). Interestingly, we did not find any fiber type-specific molecule. We hypothesize that these findings might be linked to muscle plasticity thereby facilitating a switch in the metabolic properties of fibers in response to different conditions such as exercise and diet, among others. Despite the shallow chemical gradients, cardiolipins (CLs), acylcarnitines (CAR), monoglycerides (MGs), fatty acids, highly polyunsaturated phospholipids, and oxidized phospholipids, were identified as molecular signatures of oxidative metabolism. In contrast, histidine-related compounds were found as molecular signatures of glycolytic fibers. Additionally, the presence of highly polyunsaturated acyl chains in phospholipids was found in oxidative fibers whereas more saturated acyl chains in phospholipids were found in glycolytic fibers which suggests an effect of the membrane fluidity on the metabolic properties of skeletal myofibers.

Identifiers

PMID37063787
PMCPMC10094364
OpenAlexW4360780566

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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.