journal article·2023-06-14

Heparin Affinity-Based IL-4 Delivery to Modulate Macrophage Phenotype and Endothelial Cell Activity In Vitro

Fan Zhang, Jessica M. Gluck, Ashley C. Brown, David A. Zaharoff, Martin W. King

ACS Applied Materials & Interfaces· Volume 15· Issue 23
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Abstract

Macrophages play a pivotal role in wound healing and tissue regeneration, as they are rapidly recruited to the site of injury or implanted foreign material. Depending on their interaction with the material, macrophages can develop different phenotypes, with the M1 pro-inflammatory and M2 pro-regenerative phenotypes being highly involved in tissue regeneration. M2 macrophages mitigate inflammation and promote tissue regeneration and extracellular matrix remodeling. In this study, we engineered a gelatin-heparin-methacrylate (GelMA-HepMA) hydrogel that gradually releases interleukin-4 (IL-4), a cytokine that modulates macrophages to adopt the M2 phenotype. Methacrylation of heparin improved the retention of both heparin and IL-4 within the hydrogel. The GelMA-HepMA hydrogel and IL-4 synergistically downregulated M1 gene expression and upregulated M2 gene expression in macrophages within 48 h of in vitro cell culture. However, the M2-like macrophage phenotype induced by the GelMA-HepMA-IL-4 hydrogel did not necessarily further improve endothelial cell proliferation and migration in vitro .
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Wound Healing and Treatments · Immune cells in cancer · Nerve injury and regeneration

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Wilson College of Textiles, North Carolina State University, Raleigh, North Carolina 27606, United States

Joint Department of Biomedical Engineering of University of North Carolina, Chapel Hill and North Carolina State University, Raleigh, North Carolina 27695, United States

Comparative Medicine Institute, North Carolina State University, Raleigh, North Carolina 27606, United States

Funding

North Carolina State University · Division of Biological Infrastructure · North Carolina Textile Foundation · American Association of Textile Chemists and Colorists

References (31)

Show source-provided references
1. 10.1126/sciadv.aay639110.1126/sciadv.aay6391 ↗
2. 10.1002/adhm.20220004510.1002/adhm.202200045 ↗
3. 10.1038/s41551-016-000710.1038/s41551-016-0007 ↗
4. 10.1038/s41536-021-00193-510.1038/s41536-021-00193-5 ↗
5. 10.1002/adhm.20170028910.1002/adhm.201700289 ↗
6. 10.1002/adhm.20190135810.1002/adhm.201901358 ↗
7. 10.1039/d2sm01190e10.1039/d2sm01190e ↗
8. 10.1002/adhm.20180145110.1002/adhm.201801451 ↗
9. 10.1038/s41467-020-15361-210.1038/s41467-020-15361-2 ↗
10. 10.1016/j.biomaterials.2015.10.02010.1016/j.biomaterials.2015.10.020 ↗
11. 10.1016/j.biomaterials.2019.01.04910.1016/j.biomaterials.2019.01.049 ↗
12. 10.1074/jbc.ra119.01241910.1074/jbc.ra119.012419 ↗
13. 10.1038/nprot.2016.03710.1038/nprot.2016.037 ↗
14. 10.1002/mabi.20170015810.1002/mabi.201700158 ↗
15. 10.1021/nn406019m10.1021/nn406019m ↗
16. 10.1088/1748-605x/aacdb210.1088/1748-605x/aacdb2 ↗
17. 10.1016/j.biomaterials.2008.08.01110.1016/j.biomaterials.2008.08.011 ↗
18. 10.1088/1748-605x/aca4b210.1088/1748-605x/aca4b2 ↗
19. 10.1016/j.biomaterials.2014.02.01210.1016/j.biomaterials.2014.02.012 ↗
20. 10.1016/j.actbio.2018.02.03210.1016/j.actbio.2018.02.032 ↗
21. 10.1172/jci8258510.1172/jci82585 ↗
22. 10.1371/journal.pone.019104010.1371/journal.pone.0191040 ↗
23. 10.2217/rme-2016-014110.2217/rme-2016-0141 ↗
24. 10.1007/s10456-018-9634-510.1007/s10456-018-9634-5 ↗
25. 10.1172/jci.insight.13544610.1172/jci.insight.135446 ↗
26. 10.1002/term.278910.1002/term.2789 ↗
27. 10.1158/1541-7786.mcr-11-050710.1158/1541-7786.mcr-11-0507 ↗
28. 10.1002/jcp.2170610.1002/jcp.21706 ↗
29. 10.1038/cr.2008.32610.1038/cr.2008.326 ↗
30. 10.1161/atvbaha.121.31378810.1161/atvbaha.121.313788 ↗
31. 10.1016/j.actbio.2021.04.01010.1016/j.actbio.2021.04.010 ↗