Tissue engineering;
Retinal stem and progenitor cells;
Endothelial cells;
3D and 2D co-culture;
VASCULAR NICHE;
BASEMENT-MEMBRANE;
GROWTH-FACTOR;
DIFFERENTIATION;
ANGIOGENESIS;
EYE;
NEUROGENESIS;
SCAFFOLDS;
MIGRATION;
THERAPY;
D O I:
10.1016/j.biomaterials.2012.03.062
中图分类号:
R318 [生物医学工程];
学科分类号:
100103 [病原生物学];
摘要:
Cell cell interactions are critical to understanding functional tissues. A number of stem cell populations have been shown to receive key regulatory information from endothelial cells (ECs); however, the role of ECs in the retinal stem and progenitor cell (RSPC) niche has been largely unexplored. To gain greater insight into the role of ECs on RSPC fate, a three-dimensional (3D) co-culture model, incorporating cell cell interactions, was designed by covalently-modifying agarose hydrogels with growth factors and cell-adhesive peptides in defined volumes. Therein ECs adopted tubular-like morphologies similar to those observed in vivo, but not observed in two-dimensional (2D) cultures. Unexpectedly, ECs inhibited proliferation and differentiation of RSPCs, revealing, for the first time, the possible role of ECs on RSPC fate. This 3D hydrogel scaffold provides a simple, reproducible and versatile method with which to answer biological questions related to the cellular microenvironment. (C) 2012 Elsevier Ltd. All rights reserved.