| Literature DB >> 25047627 |
Dilip Thomas1, Gianluca Fontana2, Xizhe Chen3, Clara Sanz-Nogués3, Dimitrios I Zeugolis2, Peter Dockery4, Timothy O'Brien3, Abhay Pandit5.
Abstract
Development of cell delivery platforms have been driven based on an empirical cytoprotective design. While cell-matrix and cell-cell interactions that influence biochemical effects beyond survival has been limited and overshadowed in an effort to incrementally improve biomimicking properties of the tissue-engineered constructs. Here we demonstrate fabrication of a shape controlled 3D type-I collagen-based microgel platform that can be tuned to modulate angiogenic paracrine- 'angiocrine' responses of human mesenchymal stem cells (hMSCs). Furthermore, these microgels were characterized as a 3D cell culture tool to assess optimal biological response as a function of cell-matrix and cell-cell interactions. Finally, optimised hMSC embedded microgels were shown to induce vascular repair and functional improvement in vivo in a mouse model of hind-limb ischemia. The approach described here in designing a tuneable cell delivery platform using naturally occurring extracellular matrix molecules highlights the need for highly customised matrices with an array of self-assembling proteins that dictate specific cell function resembling the native tissue of interest for repair.Entities:
Keywords: Angiogenesis; Cell-factories; Customised ECM matrices; Mesenchymal stem cells; Microgels
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Year: 2014 PMID: 25047627 DOI: 10.1016/j.biomaterials.2014.06.053
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479