⮝ Full datasets listing

PXD061227-1

PXD061227 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleA comparison of human skeletal muscle cell maturation in 2D versus 3D culture: A quantitative proteomic study C4PR_LIV
DescriptionBackground Three-dimensional (3D) bioengineered models of human skeletal muscle are a promising approach for studying muscle development, function and disease in vitro. These models more closely resemble the complexity of native muscle tissue than two-dimensional (2D) monolayer culture and allow for functional measurements to be performed. However, a more complete understanding of how culture condition and duration impacts the myotube maturity and function is required to validate the transition from 2D to 3D culture of muscle cells. Methods Human skeletal muscle cells were cultured as either 2D monolayers or within 3D fibrin-based hydrogels as muscle constructs for up to 21 days. Quantitative proteomic analysis and functional assessments, including contractile force and cross-sectional area measurements, were conducted to evaluate the impact of culture conditions and duration on muscle cell differentiation. Results Proteomic analysis revealed myoblasts differentiated into myotubes by 8 days of differentiation in both 2D and 3D environments. However, the proteomic profiles of myotubes varied significantly between the two culture environments. At day 8 of differentiation, myosin heavy chain isotype abundance indicated a predominantly slow-twitch phenotype in 3D constructs, compared to a mixed fibre type phenotype in 2D monolayers. By day 21 of differentiation, 3D muscle constructs displayed improved mitochondrial maturity, extracellular matrix remodelling, and signs of transitioning towards a fast-twitch phenotype. This prolonged culture duration also resulted in increased passive tension but decreased peak contractile force in 3D muscle constructs. Conclusions This study demonstrates that 3D culture promotes maturity in human skeletal muscle cells, mimicking the biochemical cues and energy demands seen in native muscle tissue. The data highlights the importance of selecting appropriate culture conditions and durations when studying skeletal muscle cells in vitro and suggests 8 days of differentiation as optimal for achieving peak contractile force in 3D muscle constructs.
HostingRepositoryPRIDE
AnnounceDate2025-06-23
AnnouncementXMLSubmission_2025-06-22_16:49:21.598.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterPhilip Brownridge
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListiodoacetamide derivatized residue
InstrumenttimsTOF HT
Dataset History
RevisionDatetimeStatusChangeLog Entry
02025-02-26 06:33:05ID requested
12025-06-22 16:49:22announced
Publication List
Tollitt BR, Jones SW, Ohana J, Henstock JR, Jackson MJ, McArdle A, A comparison of human skeletal muscle cell maturation in 2D versus 3D culture: A quantitative proteomic study. Physiol Rep, 13(12):e70420(2025) [pubmed]
10.14814/phy2.70420;
Keyword List
submitter keyword: Bioengineering, In vitro models, Skeletal muscle, Maturation, Proteomics, 3D culture, Hydrogel
Contact List
Professor Anne McArdle
contact affiliationInstitute of Life Course & Medical Sciences Faculty of Health and Life Sciences University of Liverpool Liverpool UK
contact emailmdcr02@liverpool.ac.uk
lab head
Philip Brownridge
contact affiliationUniversity of Liverpool
contact emailphilipjb@liv.ac.uk
dataset submitter
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2025/06/PXD061227
PRIDE project URI
Repository Record List
[ + ]