| Literature DB >> 27741500 |
Mirko Nowak1, Uwe Freudenberg1, Mikhail V Tsurkan1, Carsten Werner1, Kandice R Levental2.
Abstract
Matrix systems used to study complex three-dimensional (3D) cellular processes like mammary epithelial tissue morphogenesis and tumorigenesis ex vivo often require ill-defined biological components, which lead to poor reproducibility and a lack of control over physical parameters. In this study, a well-defined, tunable synthetic biohybrid hydrogel composed of the glycosaminoglycan heparin, star-shaped poly(ethylene glycol) (starPEG), and matrix metalloproteinase- (MMP-) cleavable crosslinkers was applied to dissect the biophysical and biochemical signals promoting human mammary epithelial cell (MEC) morphogenesis. We show that compliant starPEG-heparin matrices promote the development of polarized MEC acini. Both the presence of heparin and MMP-cleavable crosslinks are essential in facilitating MEC morphogenesis without supplementation of exogenous adhesion ligands. In this system, MECs secrete and organize laminin in basement membrane-like assemblies to promote integrin signaling and drive acinar development. Therefore, starPEG-heparin hydrogels provide a versatile platform to study mammary epithelial tissue morphogenesis in a chemically defined and precisely tunable 3D in vitro microenvironment. The system allows investigation of biophysical and biochemical aspects of mammary gland biology and potentially a variety of other organoid culture studies.Entities:
Keywords: Biomimetic material; Cell-material interaction; Heparin; Mammary epithelium; Organoid morphogenesis
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Year: 2016 PMID: 27741500 PMCID: PMC5121086 DOI: 10.1016/j.biomaterials.2016.10.007
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479