Evidence map›Paper›PMID 37439037›Full record

ArticleJournal of cachexia, sarcopenia and muscle2023

A single-cell atlas of bovine skeletal muscle reveals mechanisms regulating intramuscular adipogenesis and fibrogenesis.

Leshan Wang, Peidong Gao, Chaoyang Li, Qianglin Liu, Zeyang Yao, Yuxia Li, Xujia Zhang, Jiangwen Sun, Constantine Simintiras, Matthew Welborn and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

39 citing papers in PubMed, 47 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

14 authors at 4 institutions in 1 country.

Leshan WangSchool of Animal Science, Louisiana State University Agricultural Center, Baton Rouge, LA, USA.
Peidong GaoSchool of Animal Science, Louisiana State University Agricultural Center, Baton Rouge, LA, USA.
Chaoyang LiSchool of Animal Science, Louisiana State University Agricultural Center, Baton Rouge, LA, USA.
Qianglin LiuSchool of Animal Science, Louisiana State University Agricultural Center, Baton Rouge, LA, USA.
Zeyang YaoDepartment of Computer Science, Old Dominion University, Norfolk, VA, USA.
Yuxia LiSchool of Animal Science, Louisiana State University Agricultural Center, Baton Rouge, LA, USA.
Xujia ZhangSchool of Animal Science, Louisiana State University Agricultural Center, Baton Rouge, LA, USA.
Jiangwen SunDepartment of Computer Science, Old Dominion University, Norfolk, VA, USA.
Constantine SimintirasSchool of Animal Science, Louisiana State University Agricultural Center, Baton Rouge, LA, USA.
Matthew WelbornSchool of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, USA.
Kenneth McMillinSchool of Animal Science, Louisiana State University Agricultural Center, Baton Rouge, LA, USA.
Stephanie OprescuDepartment of Animal Sciences, Purdue University, West Lafayette, IN, USA.
Shihuan KuangDepartment of Animal Sciences, Purdue University, West Lafayette, IN, USA.
Xing FuSchool of Animal Science, Louisiana State University Agricultural Center, Baton Rouge, LA, USA.ORCID 0000-0001-5419-2691
Louisiana State University Agricultural Center · USOld Dominion University · USPurdue University West Lafayette · USLouisiana State University · US

Funding

The role of adipocyte-driven inflammation and leptin pathway in pulmonary viral infections caused by SARS-CoV-2 and influenza A virusesP20GM130555 · NIGMS · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI Konstantin G Kousoulas · 2019 to 2026
$19.9M
Immunomyoblasts in muscle regenerationR01AR078695 · NIAMS · PURDUE UNIVERSITY · PI KUANG, SHIHUAN · 2021 to 2025
$2.2M
The function of Runx1 in cardiac fibroblasts and post-myocardial infarction healingR01HL157519 · NHLBI · LOUISIANA STATE UNIV AGRICULTURAL CENTER · PI Xing Fu · 2022 to 2026
$2.1M
Tcf21 and visceral adipose tissue development and expansionR15DK122383 · NIDDK · LOUISIANA STATE UNIV AGRICULTURAL CENTER · PI FU, XING · 2019 to 2019
$409k
Sox11 function in muscle stem cellsF31AR077424 · NIAMS · PURDUE UNIVERSITY · PI OPRESCU, STEPHANIE NICOLE · 2020 to 2022
$114k
NHLBI NIH HHS R01 HL157519NIAMS NIH HHS F31 AR077424NIAMS NIH HHS R01 AR078695NIDDK NIH HHS R15 DK122383NIGMS NIH HHS P20 GM130555
6 · The paper itself

Abstract

backgroundIntramuscular fat (IMF) and intramuscular connective tissue (IMC) are often seen in human myopathies and are central to beef quality. The mechanisms regulating their accumulation remain poorly understood. Here, we explored the possibility of using beef cattle as a novel model for mechanistic studies of intramuscular adipogenesis and fibrogenesis.

methodsSkeletal muscle single-cell RNAseq was performed on three cattle breeds, including Wagyu (high IMF), Brahman (abundant IMC but scarce IMF), and Wagyu/Brahman cross. Sophisticated bioinformatics analyses, including clustering analysis, gene set enrichment analyses, gene regulatory network construction, RNA velocity, pseudotime analysis, and cell-cell communication analysis, were performed to elucidate heterogeneities and differentiation processes of individual cell types and differences between cattle breeds. Experiments were conducted to validate the function and specificity of identified key regulatory and marker genes. Integrated analysis with multiple published human and non-human primate datasets was performed to identify common mechanisms.

resultsA total of 32 708 cells and 21 clusters were identified, including fibro/adipogenic progenitor (FAP) and other resident and infiltrating cell types. We identified an endomysial adipogenic FAP subpopulation enriched for COL4A1 and CFD (log2FC = 3.19 and 1.92, respectively; P < 0.0001) and a perimysial fibrogenic FAP subpopulation enriched for COL1A1 and POSTN (log2FC = 1.83 and 0.87, respectively; P < 0.0001), both of which were likely derived from an unspecified subpopulation. Further analysis revealed more progressed adipogenic programming of Wagyu FAPs and more advanced fibrogenic programming of Brahman FAPs. Mechanistically, NAB2 drives CFD expression, which in turn promotes adipogenesis. CFD expression in FAPs of young cattle before the onset of intramuscular adipogenesis was predictive of IMF contents in adulthood (R

conclusionsOur study demonstrates the feasibility of beef cattle as a model for studying IMF and IMC. We illustrate the FAP programming during intramuscular adipogenesis and fibrogenesis and reveal the reliability of CFD as a predictor and biomarker of IMF accumulation in cattle and humans.

Indexed as

AdipogenesisMuscular Dystrophy, DuchenneAgedAnimalsCattleCell DifferentiationHumansMiceMuscle, SkeletalReproducibility of ResultsAdipogenesisFibro/adipogenic progenitorFibrogenesisIntramuscular adipose tissueSingle-cell RNAseq

Identifiers

PMID37439037
PMCPMC10570087
OpenAlexW4384120321

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.