Bio-engineering a tissue flap utilizing a porous scaffold incorporating a human induced pluripotent stem cell-derived endothelial cell capillary network connected to a vascular pedicle. (August 2019)

• Record Type: Journal Article
• Authors: Kong, Anne M.; Yap, Kiryu K.; Lim, Shiang Y.; Marre, Diego; Pébay, Alice; Gerrand, Yi-wen; Lees, Jarmon G.; Palmer, Jason A.; Morrison, Wayne A.; Mitchell, Geraldine M
• Is Part Of: Acta biomaterialia. Volume 94(2019)
• Page Start: 281
• Page End: 294
• Publication Date: 2019-08
• Subjects: Tissue flaps -- Human induced pluripotent stem cell derived endothelial cell capillary network -- NovoSorb porous scaffold -- Vascular pedicle capillary sprouting -- Silicon tissue engineering chamber; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1016/j.actbio.2019.05.067
• Languages: English
• ISSNs: 1742-7061

Abstract

Graphical abstract: Abstract: Tissue flaps are used to cover large/poorly healing wounds, but involve complex surgery and donor site morbidity. In this study a tissue flap is assembled using the mammalian body as a bioreactor to functionally connect an artery and vein to a human capillary network assembled from induced pluripotent stem cell-derived endothelial cells (hiPSC ECs). In vitro : Porous NovoSorb™ scaffolds (3 mm × 1.35 mm) were seeded with 200, 000 hiPSC ECs ± 100, 000 human vascular smooth muscle cells (hvSMC), and cultured for 1–3 days, with capillaries formed by 24 h which were CD31 +, VE-Cadherin +, EphB4 +, VEGFR2 + and Ki67 +, whilst hvSMCs (calponin + ) attached abluminally. In vivo : In SCID mice, bi-lateral epigastric vascular pedicles were isolated in a silicone chamber for a 3 week 'delay period' for pedicle capillary sprouting, then reopened, and two hiPSC EC ± hvSMCs seeded scaffolds transplanted over the pedicle. The chamber was either resealed (Group 1), or removed and surrounding tissue secured around the pedicle + scaffolds (Group 2), for 1 or 2 weeks. Human capillaries survived in vivo and were CD31 +, VE-Cadherin + and VEGFR2 + . Human vSMCs remained attached, and host mesenchymal cells also attached abluminally. Systemically injected FITC-dextran present in human capillary lumens indicated inosculation to host capillaries. Human iPSC EC capillary morphometric parameters at one week in vivo were equal to or higher than the same parameters measured in human abdominal skin. This 'proof of concept' study has demonstrated that bio-engineering an autologous human tissue flap based on hiPSC EC could minimize the use of donor flaps and has potential applications for complex wound coverage. Statement of Significance: Tissue flaps, used for surgical reconstruction of wounds, require complex surgery, often associated with morbidity. Bio-engineering a simpler alternative, we assembled a human induced pluripotent stem cell derived endothelial cell (hiPSC ECs) capillary network in a porous scaffold in vitro, which when transplanted over a mouse vascular pedicle in vivo formed a functional tissue flap with mouse blood flow in the human capillaries. Therefore it is feasible to form an autologous tissue flap derived from a hiPSC EC capillary network assembled in vitro, and functionally connect to a vascular pedicle in vivo that could be utilized in complex wound repair for chronic or acute wounds.