Coordination between ECM and cell-cell adhesion regulates the development of islet aggregation, architecture, and functional maturation
Pancreatic islets are 3-dimensional cell aggregates consisting of unique cellular composition, cell-to-cell contacts, and interactions with blood vessels. Cell aggregation is essential for islet endocrine function; however, it remains unclear how developing islets establish aggregation. By combining genetic animal models, imaging tools, and gene expression profiling, we demonstrate that islet aggregation is regulated by extracellular matrix signaling and cell-cell adhesion. Islet endocrine cell-specific inactivation of extracellular matrix receptor Integrin {beta}1 disrupted blood vessel interactions but promoted cell-cell adhesion and the formation of larger islets. In contrast, ablation of cell-cell adhesion molecule -Catenin promoted blood vessel interactions yet compromised islet clustering. Simultaneous removal of Integrin {beta}1 and -Catenin disrupts islet aggregation and the endocrine cell maturation process, demonstrating that establishment of islet aggregates is essential for functional maturation. Our study provides new insights into understanding the fundamental self-organizing mechanism for islet aggregation, architecture, and functional maturation. HIGHLIGHTSO_LIIslet vascularization and aggregation are regulated via ECM-Itgb1 signaling C_LIO_LIECM-Itgb1 signaling negatively controls islet aggregation via regulation of cell-cell adhesion during development C_LIO_LICell-cell adhesion negatively regulates the interaction of endocrine cell-vasculature in islets C_LIO_LIDifferential cell adhesion regulates the establishment of islet architecture C_LIO_LIEndocrine functional maturation depends on islet aggregation regulated by the coordination of ECM-Itgb1 signaling and cell-cell adhesion C_LI