4.5 Article

Repopulation of decellularized organ scaffolds with human pluripotent stem cell-derived pancreatic progenitor cells

期刊

BIOMEDICAL MATERIALS
卷 18, 期 2, 页码 -

出版社

IOP Publishing Ltd
DOI: 10.1088/1748-605X/acb7bf

关键词

decellularized; organ; scaffolds; decellularized organ; human pluripotent stem cell

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Diabetes is a global epidemic affecting more than 285 million people worldwide. Engineering endocrine pancreas tissue using regenerative cell source shows promise for diabetes therapy. Researchers demonstrate the feasibility of re-engineering decellularized organ scaffolds using human pluripotent stem cells (hPSC) to repopulate these scaffolds. The study finds that hPSCs cultured and differentiated as aggregates are more suitable for repopulation, especially in decellularized liver scaffolds, which also support the endocrine cell fate of the engrafted cells. This novel strategy has potential applications in preclinical testing, drug discovery, and diabetes therapy.
Diabetes is an emerging global epidemic that affects more that 285 million people worldwide. Engineering of endocrine pancreas tissue holds great promise for the future of diabetes therapy. Here we demonstrate the feasibility of re-engineering decellularized organ scaffolds using regenerative cell source. We differentiated human pluripotent stem cells (hPSC) toward pancreatic progenitor (PP) lineage and repopulated decellularized organ scaffolds with these hPSC-PP cells. We observed that hPSCs cultured and differentiated as aggregates are more suitable for organ repopulation than isolated single cell suspension. However, recellularization with hPSC-PP aggregates require a more extensive vascular support, which was found to be superior in decellularized liver over the decellularized pancreas scaffolds. Upon continued culture for nine days with chemical induction in the bioreactor, the seeded hPSC-PP aggregates demonstrated extensive and uniform cellular repopulation and viability throughout the thickness of the liver scaffolds. Furthermore, the decellularized liver scaffolds was supportive of the endocrine cell fate of the engrafted cells. Our novel strategy to engineer endocrine pancreas construct is expected to find potential applications in preclinical testing, drug discovery and diabetes therapy.

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