Uniform 40‐µm‐pore diameter precision templated scaffolds promote a pro‐healing host response by extracellular vesicle immune communication. (1st December 2020)

• Record Type: Journal Article
• Authors: Hady, Thomas F.; Hwang, Billanna; Pusic, A. D.; Waworuntu, Racheal L.; Mulligan, Michael; Ratner, Buddy; Bryers, James D.
• Is Part Of: Journal of tissue engineering and regenerative medicine. Volume 15:Number 1(2021)
• Page Start: 24
• Page End: 36
• Publication Date: 2020-12-01
• Subjects: biomaterial implant -- extracellular vesicles -- immune polarization -- macrophages -- sEV -- T cells; Tissue engineering -- Periodicals; Regeneration (Biology) -- Periodicals; 610.28
• DOI: 10.1002/term.3160
• Languages: English
• ISSNs: 1932-6254

Abstract

Abstract: Implanted porous precision templated scaffolds (PTS) with 40‐µm spherical pores reduce inflammation and foreign body reaction (FBR) while increasing vascular density upon implantation. Larger or smaller pores, however, promote chronic inflammation and FBR. While macrophage (MØ) recruitment and polarization participates in perpetuating this pore‐size‐mediated phenomenon, the driving mechanism of this unique pro‐healing response is poorly characterized. We hypothesized that the primarily myeloid PTS resident cells release small extracellular vesicles (sEVs) that induce pore‐size‐dependent pro‐healing effects in surrounding T cells. Upon profiling resident immune cells and their sEVs from explanted 40‐µm‐ (pro‐healing) and 100‐µm‐pore diameter (inflammatory) PTS, we found that PTS pore size did not affect PTS resident immune cell population ratios or the proportion of myeloid sEVs generated from explanted PTS. However, quantitative transcriptomic assessment indicated cell and sEV phenotype were pore size dependent. In vitro experiments demonstrated the ability of PTS cell‐derived sEVs to stimulate T cells transcriptionally and proliferatively. Specifically, sEVs isolated from cells inhabiting explanted 100 μm PTS significantly upregulated Th1 inflammatory gene expression in immortalized T cells. sEVs isolated from cell inhabiting both 40‐ and 100‐μm PTS upregulated essential Treg transcriptional markers in both primary and immortalized T cells. Finally, we investigated the effects of Treg depletion on explanted PTS resident cells. FoxP3+ cell depletion suggests Tregs play a unique role in balancing T cell subset ratios, thus driving host response in 40‐μm PTS. These results indicate that predominantly 40‐µm PTS myeloid cell‐derived sEVs affect T cells through a distinct, pore‐size‐mediated modality. Abstract :