Crosstalk between Macrophages and Mesenchymal Stem Cells Regulated by Biomaterials and Its Role in Bone Regeneration

Abstract

Impaired bone healing caused by severe trauma, infection, and tumor resection is an extremely common phenomenon. Therefore, the treatment of bone defects represents a major clinical challenge worldwide. In such situations, the application of biomaterials is necessary for filling defects and promoting bone regeneration. Bone repair biomaterials having osteoconductive and osteoinductive properties can act as an appropriate template for the formation of new bone and induce the osteogenic differentiation of preosteocytes and stem cells. Thus, the influence of biomaterials on the regulation of osteogenesis of mesenchymal stem cells (MSCs) has been widely studied. However, immune response is also critical in bone healing; macrophages play pivotal and dynamic roles in bone regeneration. The interfacial properties of biomaterials that affect the adsorption of proteins and the adhesion function of cells require great attention in the field of bone tissue engineering because they are related to the crosstalk with the immune and bone or stem cells. Thus, selection of biomaterials or specific surface coatings may reduce local undesirable inflammatory responses and promote bone regeneration. This review provides a detailed overview of bone regeneration mechanisms and the interaction between immune cells and MSCs. Moreover, the influence of biomaterials on the regulation of functions of MSCs and macrophages and the macrophage-related inflammatory response triggered by biomaterials and its specific role in osteogenesis are discussed.

The crosstalk between macrophages and bone marrow mesenchymal stem cells in bone healing

“…As antigen-presenting cells in immune system, Mϕs not only phagocytize pathogens or invaded foreign bodies, but also secrete cytokines to promote or inhibit inflammation [ 21 , 22 ]. After being stimulated by chemokines, monocytes migrate from bone marrow to target regions through the circulatory system and differentiate into Mϕs under the induction of macrophage colony-stimulating factor (M-CSF) and IL-4 [ 45 ]. In recent years, Mϕs are considered to be necessary for tissue regeneration in vivo [ 46 – 48 ], which is contrary to previous studies.…”