| Literature DB >> 29967223 |
Ulrich Blache1,2, Queralt Vallmajo-Martin1,3, Edward R Horton4, Julien Guerrero5, Valentin Djonov6, Arnaud Scherberich5, Janine T Erler4, Ivan Martin5, Jess G Snedeker2,7, Vincent Milleret1, Martin Ehrbar8.
Abstract
The fate of mesenchymal stem cells (MSCs) in the perivascular niche, as well as factors controlling their fate, is poorly understood. Here, we study MSCs in the perivascular microenvironment of endothelial capillaries by modifying a synthetic 3D biomimetic poly(ethylene glycol) (PEG)-hydrogel system in vitro We show that MSCs together with endothelial cells form micro-capillary networks specifically in soft PEG hydrogels. Transcriptome analysis of human MSCs isolated from engineered capillaries shows a prominent switch in extracellular matrix (ECM) production. We demonstrate that the ECM phenotypic switch of MSCs can be recapitulated in the absence of endothelial cells by functionalizing PEG hydrogels with the Notch-activator Jagged1. Moreover, transient culture of MSCs in Notch-inducing microenvironments reveals the reversibility of this ECM switch. These findings provide insight into the perivascular commitment of MSCs by use of engineered niche-mimicking synthetic hydrogels.Entities:
Keywords: Notch signaling; extracellular matrix; mesenchymal stem cell; perivascular niche; synthetic hydrogel
Mesh:
Substances:
Year: 2018 PMID: 29967223 PMCID: PMC6073216 DOI: 10.15252/embr.201845964
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807