Assessing the response of human primary macrophages to defined fibrous architectures fabricated by melt electrowriting
Source abstract
Abstract
The dual role of macrophages in the healing process depends on macrophage ability to polarize into phenotypes that can propagate inflammation or exert anti-inflammatory and tissue-remodeling functions. Controlling scaffold geometry has been proposed as a strategy to influence macrophage behavior and favor the positive host response to implants. Here, we fabricated Polycaprolactone (PCL) scaffolds by Melt Electrowriting (MEW) to investigate the ability of scaffold architecture to modulate macrophage polarization. Primary human macrophages unpolarized (M0) or polarized into M1, M2a, and M2c phenotypes were cultured on PCL films and MEW scaffolds with pore geometries (square, triangle, and rhombus grid) characterized by different angles. M0, M2a, and M2c macrophages wrapped along the fibers, while M1 macrophages formed clusters with rounded cells. Cell bridges were formed only for angles up to 90°. No relevant differences were found among PCL films and 3D scaffolds in terms of surface markers. CD206 and CD163 were highly expressed by M2a and M2c macrophages, with M2a macrophages presenting also high levels of CD86. M1 macrophages expressed moderate levels of all markers. The rhombus architecture promoted an increased release by M2a macrophages of IL10, IL13, and sCD163 compared to PCL films. The proangiogenic factor IL18 was also upregulated by the rhombus configuration in M0 and M2a macrophages compared to PCL films. The interesting findings obtained for the rhombus architecture represent a starting point for the design of scaffolds able to modulate macrophage phenotype, prompting investigations addressed to verify their ability to facilitate the healing process in vivo.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Graphene and Nanomaterials Applications · Advanced Sensor and Energy Harvesting Materials · Dielectric materials and actuators
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (65)
Show source-provided references
1. Neutrophils and macrophages: the main partners of phagocyte cell systems10.3389/fimmu.2012.00174 ↗
2. Macrophages in inflammation, repair and regeneration10.1093/intimm/dxy054 ↗
3. Metabolic features of macrophages in inflammatory diseases and cancer10.1016/j.canlet.2017.10.044 ↗
4. Macrophage activation and polarization: nomenclature and experimental guidelines10.1016/j.immuni.2014.06.008 ↗
5. Macrophage activation and polarization10.2741/2692 ↗
6. The chemokine system in diverse forms of macrophage activation and polarization10.1016/j.it.2004.09.015 ↗
7. Protective and pathogenic functions of macrophage subsets10.1038/nri3073 ↗
8. Molecular mechanisms that influence the macrophage m1-m2 polarization balance10.3389/fimmu.2014.00614 ↗
9. Macrophage polarization in chronic inflammatory diseases: killers or builders?10.1155/2018/8917804 ↗
10. Arctigenin ameliorates inflammation in vitro and in vivo by inhibiting the PI3K/AKT pathway and polarizing M1 macrophages to M2-like macrophages10.1016/j.ejphar.2013.01.014 ↗
11. Guiding synovial inflammation by macrophage phenotype modulation: an in vitro study towards a therapy for osteoarthritis10.1016/j.joca.2016.04.013 ↗
12. Macrophages sequentially change their functional phenotype in response to changes in microenvironmental influences10.4049/jimmunol.175.1.342 ↗
13. Functional plasticity of macrophages: reversible adaptation to changing microenvironments10.1189/jlb.0504272 ↗
14. Physical and mechanical regulation of macrophage phenotype and function10.1007/s00018-014-1796-8 ↗
15. Engineering biomaterials to integrate and heal: the biocompatibility paradigm shifts10.1002/bit.24559 ↗
16. Modulation of macrophage phenotype by cell shape10.1073/pnas.1308887110 ↗
17. Biomaterial based modulation of macrophage polarization: a review and suggested design principles10.1016/j.mattod.2015.01.019 ↗
18. Deconstructing the third dimension: how 3D culture microenvironments alter cellular cues
19. Micro- and nanopatterned topographical cues for regulating macrophage cell shape and phenotype10.1021/acsami.5b10589 ↗
20. Electrospun fibers and their application in drug controlled release, biological dressings, tissue repair, and enzyme immobilization10.1039/C9RA05012D ↗
21. Porous implants modulate healing and induce shifts in local macrophage polarization in the foreign body reaction10.1007/s10439-013-0933-0 ↗
22. Macrophage functional polarization (M1/M2) in response to varying fiber and pore dimensions of electrospun scaffolds10.1016/j.biomaterials.2013.02.065 ↗
23. The effect of thick fibers and large pores of electrospun poly(epsilon-caprolactone) vascular grafts on macrophage polarization and arterial regeneration10.1016/j.biomaterials.2014.03.078 ↗
24. Electrospinning polydioxanone for biomedical applications10.1016/j.actbio.2004.09.003 ↗
25. Effect of electrospun fiber diameter and alignment on macrophage activation and secretion of proinflammatory cytokines and chemokines10.1021/bm200248h ↗
26. Impact of 3-D printed PLA- and chitosan-based scaffolds on human monocyte/macrophage responses: unraveling the effect of 3-D structures on inflammation10.1016/j.actbio.2013.10.035 ↗
27. Biomaterial microarchitecture: a potent regulator of individual cell behavior and multicellular organization10.1002/jbm.a.35914 ↗
28. Direct writing by way of melt electrospinning10.1002/adma.201103482 ↗
29. Additive manufacturing of scaffolds with sub-micron filaments via melt electrospinning writing10.1088/1758-5090/7/3/035002 ↗
30. Mediating human stem cell behaviour via defined fibrous architectures by melt electrospinning writing10.1016/j.actbio.2018.05.048 ↗
31. Precisely defined fiber scaffolds with 40 mum porosity induce elongation driven M2-like polarization of human macrophages10.1088/1758-5090/ab5f4e ↗
32. The next frontier in melt electrospinning: taming the jet10.1002/adfm.201904664 ↗
33. Arthritic and non-arthritic synovial fluids modulate IL10 and IL1RA gene expression in differentially activated primary human monocytes10.1016/j.joca.2015.06.003 ↗
34. Differential gene expression in human, murine, and cell line-derived macrophages upon polarization10.1016/j.yexcr.2015.10.017 ↗
35. A culture model to analyze the acute biomaterial-dependent reaction of human primary macrophages10.1016/j.bbrc.2013.02.054 ↗
36. In vitro modulation of the behavior of adhering macrophages by medications is biomaterial-dependent10.1088/1748-605X/aa5cbc ↗
37. Measurement of DNA concentration as a normalization strategy for metabolomic data from adherent cell lines10.1021/ac401559v ↗
38. Macrophages in inflammation10.2174/1568010054022024 ↗
39. Macrophage plasticity and polarization: in vivo veritas10.1172/JCI59643 ↗
40. Design of suspended melt electrowritten fiber arrays for schwann cell migration and neurite outgrowth10.1002/mabi.202000439 ↗
41. Polymers for melt electrowriting10.1002/adhm.202001232 ↗
42. Biodegradable poly-epsilon-caprolactone (PCL) for tissue engineering applications: a review
43. Design, fabrication and characterization of PCL electrospun scaffolds—a review10.1039/c0jm04502k ↗
44. Isolation of human monocytes by double gradient centrifugation and their differentiation to macrophages in teflon-coated cell culture bags10.3791/51554-v ↗
45. Cell size of alveolar macrophages: an interspecies comparison10.1289/ehp.97105s51261 ↗
46. M2b macrophage polarization and its roles in diseases10.1002/JLB.3RU1018-378RR ↗
47. Tumor-associated macrophages: recent insights and therapies10.3389/fonc.2020.00188 ↗
48. M1 and M2a polarization of human monocyte-derived macrophages inhibits HIV-1 replication by distinct mechanisms10.4049/jimmunol.0803447 ↗
49. Alternative activation of human macrophages is rescued by estrogen treatment in vitro and impaired by menopausal status10.1210/jc.2014-2751 ↗
50. Regulation of human macrophage M1-M2 polarization balance by hypoxia and the triggering receptor expressed on myeloid cells-110.3389/fimmu.2017.01097 ↗
51. M2 polarization of human macrophages favors survival of the intracellular pathogen Chlamydia pneumoniae10.1371/journal.pone.0143593 ↗
52. Strain-dependent modulation of macrophage polarization within scaffolds10.1016/j.biomaterials.2014.03.002 ↗
53. Hemodynamic loads distinctively impact the secretory profile of biomaterial-activated macrophages - implications for in situ vascular tissue engineering10.1039/C9BM01005J ↗
54. Classification of M1/M2-polarized human macrophages by label-free hyperspectral reflectance confocal microscopy and multivariate analysis10.1038/s41598-017-08121-8 ↗
55. The role of macrophage phenotype in vascularization of tissue engineering scaffolds10.1016/j.biomaterials.2014.02.012 ↗
56. Inducing healing-like human primary macrophage phenotypes by 3D hydrogel coated nanofibres10.1016/j.biomaterials.2012.02.050 ↗
57. Inflammatory priming enhances mesenchymal stromal cell secretome potential as a clinical product for regenerative medicine approaches through secreted factors and EV-miRNAs: the example of joint disease10.1186/s13287-020-01677-9 ↗
58. Cartilage inflammation and degeneration is enhanced by pro-inflammatory (M1) macrophages in vitro, but not inhibited directly by anti-inflammatory (M2) macrophages10.1016/j.joca.2016.07.018 ↗
59. Characterizing the macrophage response to immunomodulatory biomaterials through gene set analyses10.1089/ten.tec.2019.0309 ↗
60. Response of human macrophages to wound matrices in vitro10.1111/wrr.12423 ↗
61. Overview of the IL-1 family in innate inflammation and acquired immunity10.1111/imr.12621 ↗
62. The pro- and anti-inflammatory properties of the cytokine interleukin-610.1016/j.bbamcr.2011.01.034 ↗
63. YAP-mediated mechanotransduction tunes the macrophage inflammatory response10.1126/sciadv.abb8471 ↗
64. Biophysical regulation of macrophages in health and disease10.1002/JLB.MR0318-126R ↗
65. Spatial confinement downsizes the inflammatory response of macrophages10.1038/s41563-018-0190-6 ↗