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PXD077881-1

PXD077881 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleAnimal-free three-dimensional in vitro angiogenesis tool
DescriptionAll metabolically active tissues have a dense vascular network to supply oxygen and nutrients. Angiogenesis, the formation of new blood vessels from existing ones, can be activated by the lack of oxygen in cells, disease, trauma, or tumor growth. Due to its essential role in cell survival, angiogenesis has been extensively studied, and therapeutic control of this process is of growing interest. Simultaneously, research aims to find and standardize non-animal testing methods for future use. However, the establishment of reproducible and physiologically relevant vascular networks in vitro is challenging, particularly due to the widespread use of heterogeneous animal-derived matrices which are not in keeping with goals the with the principles of the 3Rs (Replacement, Reduction, Refinement) in science and research.to reduce the use of animals in research. To address these limitations and support the development of ethical and sustainable in vitro methods, we present a novel animal-free, three-dimensional angiogenesis model based on medical grade plant-derived nanofibrillated cellulose hydrogel (NFCh). The model uses human umbilical vein endothelial cells (HUVECs) and human adipose-derived stromal cells (hASCs) cultured in medium supplemented with human serum and NFCh matrix. First, HUVECs were stimulated with stem cell-conditioned medium and cultured in varying NFCh concentrations (0.125–2.4 %) tuned to identify the optimal matrix stiffness for capillary-like structure formation. HUVECs were then cocultured with adipose-derived stromal cellshASCs in the best-performing hydrogel concentration, followed by imaging and proteomics analysis. We observed formation of capillary-like structures, comparable to the most commonly used animal-derived extracellular matrix (ECM) control. Interestingly cells in lower NFCh concentration (0.125 %) had higher expression of wound healing and angiogenesis-related proteins while higher stiffnesses (1.5 %) had higher ECM-related protein expression. Importantly, vascular network morphology and organization could be adjusted by modifying only NFCh concentration. These findings demonstrate the potential of NFCh as a reproducible, animal-free alternative to conventional angiogenesis matrices with relevance to regenerative therapies, toxicological testing, drug screening, and the development of a 3Rs (Replacement, Reduction, Refinement)-compliant in vitro system.
HostingRepositoryPRIDE
AnnounceDate2026-08-24
AnnouncementXMLSubmission_2026-08-23_16:11:17.094.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterChris Pridgeon
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606;
ModificationListNo PTMs are included in the dataset
InstrumentBruker Daltonics timsTOF series
Dataset History
RevisionDatetimeStatusChangeLog Entry
02026-04-30 09:45:44ID requested
12026-08-23 16:11:18announced
Publication List
10.3389/ftox.2026.1768268;
Koivunotko E, Pridgeon CS, Paasonen L, Harjum, ä, ki R, angiogenesis models. Front Toxicol, 8():1768268(2026) [pubmed]
Keyword List
submitter keyword: Human, capillary-like formation, in vitro 3D cell model, animal-free, angiogenesis, nanofibrillated cellulose hydrogel, coculture
Contact List
Riina Harjumaki
contact affiliationFaculty of Pharmacy, University of Helsinki, Helsinki, Finland.
contact emailriina.harjumaki@helsinki.fi
lab head
Chris Pridgeon
contact affiliationUniversity of Helsinki
contact emailpridgeonc@gmail.com
dataset submitter
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Dataset FTP location
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PRIDE project URI
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