Macrophage activation in response to shape memory polymer foam‐coated aneurysm occlusion devices

Brain aneurysms can be treated with embolic coils using minimally invasive approaches. It is advantageous to modulate the biologic response of platinum embolic coils. Our previous studies demonstrated that shape memory polymer (SMP) foam coated embolization coils (FCC) devices demonstrate enhanced h...

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Veröffentlicht in:Journal of biomedical materials research. Part B, Applied biomaterials Applied biomaterials, 2022-07, Vol.110 (7), p.1535-1544
Hauptverfasser: Chau, Sarah M., Herting, Scott M., Noltensmeyer, Dillon A., Ahmed, Hamzah, Maitland, Duncan J., Raghavan, Shreya
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container_issue 7
container_start_page 1535
container_title Journal of biomedical materials research. Part B, Applied biomaterials
container_volume 110
creator Chau, Sarah M.
Herting, Scott M.
Noltensmeyer, Dillon A.
Ahmed, Hamzah
Maitland, Duncan J.
Raghavan, Shreya
description Brain aneurysms can be treated with embolic coils using minimally invasive approaches. It is advantageous to modulate the biologic response of platinum embolic coils. Our previous studies demonstrated that shape memory polymer (SMP) foam coated embolization coils (FCC) devices demonstrate enhanced healing responses in animal models compared with standard bare platinum coil (BPC) devices. Macrophages are the most prevalent immune cell type that coordinate the greater immune response to implanted materials. Hence, we hypothesized that the highly porous SMP foam coatings on embolic coils activate a pro‐regenerative healing phenotype. To test this hypothesis, we analyzed the number and type of infiltrating macrophages in FCC or BPC devices implanted in a rabbit elastase aneurysm model. FCC devices elicited a great number of infiltration macrophages, skewed significantly to a pro‐regenerative M2‐like phenotype 90 days following implantation. We devised an in vitro assay, where monocyte‐derived macrophages were placed in close association with FCC or BPC devices for 6–72 h. Macrophages encountering SMP FCC‐devices demonstrated highly mixed activation phenotypes at 6 h, heavily skewing toward an M2‐like phenotype by 72 h, compared with macrophages encountering BPC devices. Macrophage activation was evaluated using gene expression analysis, and secreted cytokine evaluation. Together, our results demonstrate that FCC devices promoted a pro‐regenerative macrophage activation phenotype, compared with BPC devices. Our in vitro findings corroborate with in vivo observations that SMP‐based modification of embolic coils can promote better healing of the aneurysm site, by sustaining a pro‐healing macrophage phenotype.
doi_str_mv 10.1002/jbm.b.35015
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It is advantageous to modulate the biologic response of platinum embolic coils. Our previous studies demonstrated that shape memory polymer (SMP) foam coated embolization coils (FCC) devices demonstrate enhanced healing responses in animal models compared with standard bare platinum coil (BPC) devices. Macrophages are the most prevalent immune cell type that coordinate the greater immune response to implanted materials. Hence, we hypothesized that the highly porous SMP foam coatings on embolic coils activate a pro‐regenerative healing phenotype. To test this hypothesis, we analyzed the number and type of infiltrating macrophages in FCC or BPC devices implanted in a rabbit elastase aneurysm model. FCC devices elicited a great number of infiltration macrophages, skewed significantly to a pro‐regenerative M2‐like phenotype 90 days following implantation. We devised an in vitro assay, where monocyte‐derived macrophages were placed in close association with FCC or BPC devices for 6–72 h. Macrophages encountering SMP FCC‐devices demonstrated highly mixed activation phenotypes at 6 h, heavily skewing toward an M2‐like phenotype by 72 h, compared with macrophages encountering BPC devices. Macrophage activation was evaluated using gene expression analysis, and secreted cytokine evaluation. Together, our results demonstrate that FCC devices promoted a pro‐regenerative macrophage activation phenotype, compared with BPC devices. Our in vitro findings corroborate with in vivo observations that SMP‐based modification of embolic coils can promote better healing of the aneurysm site, by sustaining a pro‐healing macrophage phenotype.</description><identifier>ISSN: 1552-4973</identifier><identifier>EISSN: 1552-4981</identifier><identifier>DOI: 10.1002/jbm.b.35015</identifier><identifier>PMID: 35090200</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Aneurysm ; Aneurysms ; Animal models ; Animals ; biomaterials ; Biomedical materials ; Blood Vessel Prosthesis ; Cell activation ; Cerebral blood flow ; Coatings ; Coils ; Cytokines ; Elastase ; Embolization ; Embolization, Therapeutic ; Endovascular coiling ; Gene expression ; Genotype &amp; phenotype ; Healing ; Immune response ; Immune system ; implantable materials ; In vivo methods and tests ; Intracranial Aneurysm - surgery ; Ischemia ; Macrophage Activation ; Macrophages ; Materials research ; Materials science ; Monocytes ; Occlusion ; Phenotypes ; Platinum ; Polymers ; Rabbits ; Shape memory ; shape memory polymers ; Smart Materials</subject><ispartof>Journal of biomedical materials research. 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source MEDLINE; Wiley Journals
subjects Aneurysm
Aneurysms
Animal models
Animals
biomaterials
Biomedical materials
Blood Vessel Prosthesis
Cell activation
Cerebral blood flow
Coatings
Coils
Cytokines
Elastase
Embolization
Embolization, Therapeutic
Endovascular coiling
Gene expression
Genotype & phenotype
Healing
Immune response
Immune system
implantable materials
In vivo methods and tests
Intracranial Aneurysm - surgery
Ischemia
Macrophage Activation
Macrophages
Materials research
Materials science
Monocytes
Occlusion
Phenotypes
Platinum
Polymers
Rabbits
Shape memory
shape memory polymers
Smart Materials
title Macrophage activation in response to shape memory polymer foam‐coated aneurysm occlusion devices
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