Macromechanics and polycaprolactone fiber organization drive macrophage polarization and regulate inflammatory activation of tendon in vitro and in vivo. (August 2020)

• Record Type: Journal Article
• Authors: Schoenenberger, Angelina D.; Tempfer, Herbert; Lehner, Christine; Egloff, Jasmin; Mauracher, Marita; Bird, Anna; Widmer, Jonas; Maniura-Weber, Katharina; Fucentese, Sandro F.; Traweger, Andreas; Silvan, Unai; Snedeker, Jess G.
• Is Part Of: Biomaterials. Volume 249(2020:Jul.)
• Publication Date: 2020-08
• Subjects: Topography -- Nanofibers -- Inflammation -- Macrophage -- Mechanobiology -- Tendon; Biomedical materials -- Periodicals; Biocompatible Materials -- Periodicals; Biomatériaux -- Périodiques; 610.28
• DOI: 10.1016/j.biomaterials.2020.120034
• Languages: English
• ISSNs: 0142-9612

Abstract

Abstract: Appropriate macrophage response to an implanted biomaterial is crucial for successful tissue healing outcomes. In this work we investigated how intrinsic topological cues from electrospun biomaterials and extrinsic mechanical loads cooperate to guide macrophage activation and macrophage-tendon fibroblast cross-talk. We performed a series of in vitro and in vivo experiments using aligned or randomly oriented polycaprolactone nanofiber substrates in both mechanically loaded and unloaded conditions. Across all experiments a disorganized biomaterial fiber topography was alone sufficient to promote a pro-inflammatory signature in macrophages, tendon fibroblasts, and tendon tissue. Extrinsic mechanical loading was found to strongly regulate the character of this signature by reducing pro-inflammatory markers both in vitro and in vivo . We observed that macrophages generally displayed a stronger response to biophysical cues than tendon fibroblasts, with dominant effects of cross-talk between these cell types observed in mechanical co-culture models. Collectively our data suggest that macrophages play a potentially important role as mechanosensory cells in tendon repair, and provide insight into how biological response might be therapeutically modulated by rational biomaterial designs that address the biomechanical niche of recruited cells. Graphical abstract: Image 1