Basement membrane proteins modulate cell migration on bovine pericardium extracellular matrix scaffold

Native bovine pericardium (BP) exhibits anisotropy of its surface ECM niches, with the serous surface (i.e., parietal pericardium) containing basement membrane components (e.g., Laminin, Col IV) and the fibrous surface (i.e., mediastinal side) being composed primarily of type I collagen (Col I). Native BP surface ECM niche anisotropy is preserved in antigen removed BP (AR-BP) extracellular matrix (ECM) scaffolds. By exploiting sideness (serous or fibrous surface) of AR-BP scaffolds, this study aims to determine the mechanism by which ECM niche influences human mesenchymal stem cells (hMSCs) migration. Human mesenchymal stem cells (hMSC) seeding on serous surface promoted more rapid cell migration than fibrous surface seeding. Gene analysis revealed that expression of integrin alpha (3) and alpha (11) were increased in cells cultured on serous surface compared to those on the fibrous side. Monoclonal antibody blockade of alpha (3)beta (1) (i.e., laminin binding) inhibited early (i.e.<= 6 h) hMSC migration following serous seeding, while having no effect on migration of cells on the fibrous side. Blockade of alpha (3)beta (1) resulted in decreased expression of integrin alpha (3) by cells on serous surface. Monoclonal antibody blockade of alpha (11)beta (1) (i.e., Col IV binding) inhibited serous side migration at later time points (i.e., 6-24 h). These results confirmed the role of integrin alpha (3)beta (1) binding to laminin in mediating early rapid hMSCs migration and alpha (11)beta (1) binding to Col IV in mediating later hMSCs migration on the serous side of AR-BP, which has critical implications for rate of cellular monolayer formation and use of AR-BP as blood contacting material for clinical applications.

Automated summary

The study found that human mesenchymal stem cells migrated faster on the serous surface than on the fibrous surface, potentially due to increased expression of integrin alpha (3) and alpha (11). Blockade of integrin alpha (3)beta (1) inhibited early hMSC migration on the serous side, while blockade of alpha (11)beta (1) inhibited later hMSC migration.