Ovarian extracellular matrix-based hydrogel for human ovarian follicle survival in vivo: A pilot work.
Maria-Costanza ChitiJulie VanackerEmna OuniNatalija TaticAiswarya ViswanathAnne des RieuxMarie-Madeleine DolmansLisa Jane WhiteChristiani Andrade AmorimPublished in: Journal of biomedical materials research. Part B, Applied biomaterials (2021)
To successfully assemble a bio-engineered ovary, we need to create a three-dimensional matrix able to accommodate isolated follicles and cells. The goal of this study was to develop an extracellular matrix hydrogel (oECM) derived from decellularized bovine ovaries able to support, in combination with alginate, human ovarian follicle survival and growth in vitro. Two different hydrogels (oECM1, oECM2) were produced and compared in terms of decellularization efficiency (dsDNA), ECM preservation (collagen and glycosaminoglycan levels), ultrastructure, rigidity, and cytotoxicity. oECM2 showed significantly less dsDNA, greater retention of glycosaminoglycans and better rigidity than oECM1. Isolated human ovarian follicles were then encapsulated in four selected hydrogel combinations: (1) 100% oECM2, (2) 90% oECM2 + 10% alginate, (3) 75% oECM2 + 25% alginate, and (4) 100% alginate. After 1 week of in vitro culture, follicle recovery rate, viability, and growth were analyzed. On day 7 of in vitro culture, follicle recovery rates were 0%, 23%, 65%, 82% in groups 1-4, respectively, rising proportionally with increased alginate content. However, there was no difference in follicle viability or growth between groups 2 and 3 and controls (group 4). In conclusion, since pure alginate cannot be used to graft preantral follicles due to its poor revascularization and degradation after grafting, oECM2 hydrogel combined with alginate may provide a new and promising alternative to graft isolated human follicles in a bio-engineered ovary.
Keyphrases
- extracellular matrix
- tissue engineering
- wound healing
- endothelial cells
- drug delivery
- induced pluripotent stem cells
- pluripotent stem cells
- hyaluronic acid
- coronary artery disease
- randomized controlled trial
- clinical trial
- atrial fibrillation
- cell proliferation
- endoplasmic reticulum stress
- drug release
- free survival
- cell cycle arrest