In vitro differentiation of human amniotic epithelial cells into insulin-producing 3D spheroids

Author:

Okere Bernard1,Alviano Francesco2,Costa Roberta2,Quaglino Daniela3,Ricci Francesca4,Dominici Massimo5,Paolucci Paolo1,Bonsi Laura2,Iughetti Lorenzo1

Affiliation:

1. Division of Pediatric Oncology, Hematology and Marrow Transplantation, Department of Medical and Surgical Sciences for Children & Adults, University of Modena and Reggio Emilia, Modena Policlinic, Modena, Italy

2. Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy

3. Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy

4. Immunohematology and Transfusion Medicine Service, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy

5. Division of Oncology, Department of Medical and Surgical Sciences for Children & Adults, University of Modena and Reggio Emilia, Modena Policlinic, Modena, Italy

Abstract

Regenerative medicine and stem cell therapy may represent the solution for the treatment of non-curable human diseases such as type 1 diabetes. In this context of growing demand for functional and safe stem cells, human amniotic epithelial cells (hAECs) from term placenta have attracted increasing interest for their wide availability, stem cell properties, and differentiation plasticity, which make them a promising tool for stem cell-based therapeutic applications. We initially assayed the stemness characteristics of hAECs in serum-free conditions. Subsequently we developed a culture procedure on extracellular matrix for the formation of three-dimensional (3D) spheroids. Finally, we tested the immunomodulation and differentiation potential of hAEC spheroids: the presence of pancreatic endocrine hormones was revealed with transmission electron microscopy and immunofluorescence analyses; the release of C-peptide in hyperglycemic conditions was assayed with ELISA. The serum-free culture conditions we applied proved to maintain the basic stemness characteristics of hAECs. We also demonstrated that 3D spheroids formed by hAECs in extracellular matrix can be induced to differentiate into insulin-producing cells. Finally, we proved that control and induced cells equally inhibit the proliferation of activated mononuclear cells. The results of this study highlight the properties of amnion derived epithelial cells as promising and abundant source for cell-based therapies. In particular we are the first group to show the in vitro pancreatic induction of hAECs cultured on extracellular matrix in a 3D fashion. We accordingly propose the outcomes of this study as a novel contribution to the development of future cell replacement therapies involving placenta-derived cells.

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

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