Extracellular Matrix-Based Strategies for Immunomodulatory Biomaterials Engineering.
Andrew T RowleyRaji R NagallaSzu-Wen WangWendy F LiuPublished in: Advanced healthcare materials (2019)
The extracellular matrix (ECM) is a complex and dynamic structural scaffold for cells within tissues and plays an important role in regulating cell function. Recently it has become appreciated that the ECM contains bioactive motifs that can directly modulate immune responses. This review describes strategies for engineering immunomodulatory biomaterials that utilize natural ECM-derived molecules and have the potential to harness the immune system for applications ranging from tissue regeneration to drug delivery. A top-down approach utilizes full-length ECM proteins, including collagen, fibrin, or hyaluronic acid-based materials, as well as matrices derived from decellularized tissue. These materials have the benefit of maintaining natural conformation and structure but are often heterogeneous and encumber precise control. By contrast, a bottom-up approach leverages immunomodulatory domains, such as Arg-Gly-Asp (RGD), matrix metalloproteinase (MMP)-sensitive peptides, or leukocyte-associated immunoglobulin-like receptor-1(LAIR-1) ligands, by incorporating them into synthetic materials. These materials have tunable control over immune cell functions and allow for combinatorial approaches. However, the synthetic approach lacks the full natural context of the original ECM protein. These two approaches provide a broad range of engineering techniques for immunomodulation through material interactions and hold the potential for the development of future therapeutic applications.
Keyphrases
- extracellular matrix
- hyaluronic acid
- tissue engineering
- drug delivery
- immune response
- stem cells
- magnetic resonance
- induced apoptosis
- gene expression
- human health
- magnetic resonance imaging
- cell cycle arrest
- dendritic cells
- current status
- risk assessment
- wound healing
- binding protein
- cancer therapy
- small molecule
- inflammatory response
- cell death
- molecular dynamics simulations
- bone regeneration
- cell migration