Evidence map›Paper›PMID 41549311›Full record

ArticleSkeletal muscle2026

ASB5 is a specific marker for muscle satellite cells but dispensable for skeletal muscle development and regeneration.

Muhammad Asif, Stephanie N Oprescu, Renjie Shang, Zheng Zhang, Feng Yue, Pengpeng Bi, Shihuan Kuang

Abstract read
In one paragraph

Article in Skeletal muscle, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Muhammad AsifDepartment of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC, 27710, USA.
Stephanie N OprescuDepartment of Animal Sciences, Purdue University, West Lafayette, IN, 47907, USA.
Renjie ShangDepartment of Genetics, University of Georgia, Athens, GA, 30602, USA.
Zheng ZhangDepartment of Genetics, University of Georgia, Athens, GA, 30602, USA.
Feng YueDepartment of Animal Sciences, Purdue University, West Lafayette, IN, 47907, USA.
Pengpeng BiDepartment of Genetics, University of Georgia, Athens, GA, 30602, USA. pbi@uga.edu.
Shihuan KuangDepartment of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC, 27710, USA. Shihuan.kuang@duke.edu.

Funding

Spatial genetics investigation of multinucleated cells -Administrative Supplement - EquipmentR35GM147209 · NIGMS · UNIVERSITY OF GEORGIA · PI Pengpeng Bi · 2022 to 2026
$2.1M
Discover the Boosters of Myoblast FusionR21AR080330 · NIAMS · UNIVERSITY OF GEORGIA · PI BI, PENGPENG · 2022 to 2023
$365k
NIAMS NIH HHS R21 AR080330NIGMS NIH HHS R35 GM147209NIH HHS AR077424NIH HHS GM147209NIH HHS R01AR078695, R01AR079235, R01DK132819
6 · The paper itself

Abstract

backgroundSkeletal muscle plays a crucial role in human life, contributing to posture, movement, nutrient storage, and body temperature regulation. Development and regeneration of skeletal muscles rely on embryonic myogenic progenitors and postnatal satellite cells (MuSCs), respectively. Identification of new molecular markers and elucidating their functions in MuSCs will provide better understanding of muscle development and regeneration.

methodsWe surveyed single cell RNA-seq (scRNA-seq) data (Tabula Muris and GSE150366) to identify ASB5 (Ankyrin repeat and Suppressor of cytokine signaling Box containing 5) as a marker of MuSCs. We also used CRISPR-CAS9 genome editing and oviduct electroporation to generate a germline knockout (KO) mouse line of Asb5. We then analyzed the muscle growth and regeneration of the KO mice. We further analyzed proliferation and differentiation of MuSCs attached on myofibers. We finally performed Realtime PCR (qPCR) to examine how Asb5 KO affects gene expression in the skeletal muscle.

resultsAnalysis of data publicly available at Tabula Muris identified Asb5 as a specific marker of MuSCs. Further analysis of scRNA-seq data on FACS-purified MuSCs at various regeneration time points revealed that Asb5 is highly expressed in MuSCs and their progenies across various stages of muscle regeneration. We then generated a novel Asb5 KO mouse line through CRISPR-Cas9 deletion of Exon 4. The Asb5-KO mice were born normally and exhibited normal postnatal growth. In addition, Asb5-KO MuSCs proliferated, differentiated and self-renewed normally on myofiber explants. Furthermore, the skeletal muscles of Asb5-KO mice regenerated normally after acute injury. qPCR analysis showed that Asb5 KO reduces the expression levels of Tnfa (Tumor Necrosis Factor Alpha) in the skeletal muscles.

conclusionThese data together identify ASB5 as an abundantly expressed and specific marker of MuSCs and myogenic progenitors. However, Asb5 loss-of-function has no effects on embryonic development and postnatal growth of skeletal muscles, or behavior and regenerative functions of MuSCs under normal physiological conditions.

Indexed as

Muscle DevelopmentMuscle, SkeletalRegenerationSatellite Cells, Skeletal MuscleSuppressor of Cytokine Signaling ProteinsAnimalsBiomarkersCell DifferentiationCell ProliferationFemaleMiceMice, KnockoutBiomarkersSuppressor of Cytokine Signaling ProteinsAsb5CRISPR/Cas9MyogenesisRegenerationSatellite cellSkeletal muscle

Identifiers

PMID41549311
PMCPMC12990408

What Socratic holds

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LicenceCC BY
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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 Socratic graph.