A hybrid construct of decellularized matrix and fibrin for differentiating adipose stem cells into insulin‐producing cells, an optimized in vitro assessment.

The generation of insulin‐producing cells (IPCs) is an attractive approach for replacing damaged β cells in diabetic patients. In the present work, we introduced a hybrid platform of decellularized amniotic membrane (dAM) and fibrin encapsulation for differentiating adipose tissue‐derived stem cells (ASCs) into IPCs. ASCs were isolated from healthy donors and characterized. Human AM was decellularized, and its morphology, DNA, collagen, glycosaminoglycan (GAG) contents, and biocompatibility were evaluated. ASCs were subjected to four IPC differentiation methods, and the most efficient method was selected for the experiment. ASCs were seeded onto dAM, alone or encapsulated in fibrin gel with various thrombin concentrations, and differentiated into IPCs according to a method applying serum‐free media containing 2‐mercaptoethanol, nicotinamide, and exendin‐4. PDX‐1, GLUT‐2 and insulin expression were evaluated in differentiated cells using real‐time PCR. Structural integrity and collagen and GAG contents of AM were preserved after decellularization, while DNA content was minimized. Cultivating ASCs on dAM augmented their attachment, proliferation, and viability and enhanced the expression of PDX‐1, GLUT‐2, and insulin in differentiated cells. Encapsulating ASCs in fibrin gel containing 2 mg/ml fibrinogen and 10 units/ml thrombin increased their differentiation into IPCs. dAM and fibrin gel synergistically enhanced the differentiation of ASCs into IPCs, which could be considered an appropriate strategy for replacing damaged β cells. Significance statement: Developing strategies for replacing lost or damaged β cells in diabetic patients is attractive in regenerative medicine. In the current work, we introduced a hybrid approach of using a biological scaffold (decellularized amniotic membrane) and encapsulating biomolecules (fibrin gel) to enhance the differentiation of adipose tissue stem cells into insulin‐producing cells under specific culture conditions. Both decellularized amniotic membrane and fibrin gel effectively increased β cell markers and insulin production in differentiated cells. [ABSTRACT FROM AUTHOR]