Abstract
Macrophages are immune cells involved in wound healing and tissue regeneration; however, the sustained presence of proinflammatory macrophages in wound sites impairs healing. In this study, we shifted peritoneal macrophage polarization away from a proinflammatory (M1) phenotype through exposure to stabilized interleukin-4 (IL-4) in poly (lactic-co-glycolic acid) films in combination with topographical guidance from electro spun poly-l-lactic acid fibers. To our knowledge, this was the first study to stabilize IL-4 with bovine serum albumin (BSA) within a biomaterial. When IL-4 was coloaded with BSA for stabilization, we saw increased IL-4 bioactivity compared to no added stabilization, trehalose stabilization, or murine serum albumin stabilization. We observed increased elongation of peritoneal macrophages, increased RNA expression of anti-inflammatory marker arginase-1, increased ratio of interleukin-10/interleukin-12 p40 RNA, and decreased protein expression of proinflammatory markers (interleukin-12 p40 and RANTES) compared to controls. Taken together, these results suggest the macrophages were less proinflammatory and were a more pro-resolving phenotype. When stabilized with BSA, IL-4-loaded films effectively shift macrophage polarization state and are thus promising scaffolds to reduce inflammation within in vivo injury models.
Recommended Citation
A. M. Ziemba et al., "Stabilized Interleukin-4-Loaded Poly(lactic- Co-glycolic) Acid Films Shift Proinflammatory Macrophages toward a Regenerative Phenotype in Vitro," ACS Applied Bio Materials, vol. 2, no. 4, pp. 1498 - 1508, American Chemical Society, Apr 2019.
The definitive version is available at https://doi.org/10.1021/acsabm.8b00769
Department(s)
Chemical and Biochemical Engineering
Keywords and Phrases
cytokine stabilization; inflammation; interleukin-4; macrophage; poly(lactic- co-glycolic acid)
International Standard Serial Number (ISSN)
2576-6422
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2025 American Chemical Society, All rights reserved.
Publication Date
15 Apr 2019
PubMed ID
31061988

Comments
National Science Foundation, Grant 1150125