Molecular mechanisms of dendritic cell migration in immunity and cancer.
Charlotte M de WindeClare MundaySophie E ActonPublished in: Medical microbiology and immunology (2020)
Dendritic cells (DCs) are a heterogeneous population of antigen-presenting cells that act to bridge innate and adaptive immunity. DCs are critical in mounting effective immune responses to tissue damage, pathogens and cancer. Immature DCs continuously sample tissues and engulf antigens via endocytic pathways such as phagocytosis or macropinocytosis, which result in DC activation. Activated DCs undergo a maturation process by downregulating endocytosis and upregulating surface proteins controlling migration to lymphoid tissues where DC-mediated antigen presentation initiates adaptive immune responses. To traffic to lymphoid tissues, DCs must adapt their motility mechanisms to migrate within a wide variety of tissue types and cross barriers to enter lymphatics. All steps of DC migration involve cell-cell or cell-substrate interactions. This review discusses DC migration mechanisms in immunity and cancer with a focus on the role of cytoskeletal processes and cell surface proteins, including integrins, lectins and tetraspanins. Understanding the adapting molecular mechanisms controlling DC migration in immunity provides the basis for therapeutic interventions to dampen immune activation in autoimmunity, or to improve anti-tumour immune responses.
Keyphrases
- dendritic cells
- immune response
- papillary thyroid
- regulatory t cells
- single cell
- gene expression
- cell therapy
- squamous cell
- toll like receptor
- stem cells
- cell surface
- induced apoptosis
- air pollution
- case report
- physical activity
- childhood cancer
- biofilm formation
- young adults
- endoplasmic reticulum stress
- staphylococcus aureus
- mesenchymal stem cells
- gram negative