Silicon‐Enhanced Adipogenesis and Angiogenesis for Vascularized Adipose Tissue Engineering

The enhancement of adipogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) and sufficient vascularization remain great challenges for the successful reconstruction of engineered adipose tissue. Here, the bioactive effects of silicon (Si) ions on adipogenic differentiation of human BMSCs (HBMSCs) and the stimulation of vascularization during adipose tissue regeneration are reported. The results show that Si ions can enhance adipogenic differentiation of HBMSCs through the stimulation of the expression of adipogenic differentiation switches such as peroxisome proliferator‐activated receptor γ and CCAAT/enhancer‐binding protein α. Furthermore, Si ions can enhance both angiogenesis and adipogenesis, and inhibit dedifferentiation of cocultured adipocytes by regulating the interactions between HBMSC‐derived adipocytes and human umbilical vein endothelial cells, in which the promotion of the expression of insulin‐like growth factor 1 and vascular endothelial growth factor plays vital roles. The in vivo studies further demonstrate that the designed composite hydrogel with the ability to release bioactive Si ions clearly stimulates neovascularization and adipose tissue regeneration. The study suggests that Si ions released from biomaterials are important chemical cues for adipogenic differentiation and biomaterials with the ability to release Si ions can be designed for adipose tissue engineering. An adipose tissue engineering strategy is developed based on the bioactivity of silicon (Si) ions, which enhance adipogenic differentiation of human bone marrow mesenchymal stem cells (HBMSCs), and activate angiogenesis and adipogenesis via stimulation of the interactions of HBMSC‐derived adipocytes and human umbilical vein endothelial cells. A Si ion‐releasing hydrogel loaded with these two types of cells can stimulate vascularized adipose tissue regeneration.