TY - JOUR
T1 - Macrophage activation in response to shape memory polymer foam-coated aneurysm occlusion devices
AU - Chau, Sarah M.
AU - Herting, Scott M.
AU - Noltensmeyer, Dillon A.
AU - Ahmed, Hamzah
AU - Maitland, Duncan J.
AU - Raghavan, Shreya
N1 - Funding Information:
This work was supported by the NIH National Institute of Neurological Disorders and Stroke grant U01‐NS089692 (DJM), and the Texas A&M Engineering Experiment Station and the Department of Biomedical Engineering (SR). This project was also supported in part by a fellowship award through the National Defense Science and Engineering Graduate (NDSEG) Fellowship Program (SMH). Devices used for the in vitro studies in this article were supplied by Shape Memory Medical, Inc. Taryn Barry provided technical support in the staining and imaging of the in vivo study slides.
Funding Information:
National Institute of Neurological Disorders and Stroke, Grant/Award Number: U01‐NS089692; National Defense Science and Engineering Graduate (NDSEG) Fellowship Program (SMH); Texas A&M Engineering Experiment Station and the Department of Biomedical Engineering (SR) Funding information
Publisher Copyright:
© 2022 Wiley Periodicals LLC.
PY - 2022/7
Y1 - 2022/7
N2 - 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.
AB - 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.
KW - biomaterials
KW - immune response
KW - implantable materials
KW - macrophages
KW - shape memory polymers
KW - Rabbits
KW - Intracranial Aneurysm/surgery
KW - Blood Vessel Prosthesis
KW - Embolization, Therapeutic
KW - Macrophage Activation
KW - Animals
KW - Platinum
KW - Smart Materials
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U2 - 10.1002/jbm.b.35015
DO - 10.1002/jbm.b.35015
M3 - Article
C2 - 35090200
AN - SCOPUS:85123772511
SN - 1552-4973
VL - 110
SP - 1535
EP - 1544
JO - Journal of Biomedical Materials Research - Part B Applied Biomaterials
JF - Journal of Biomedical Materials Research - Part B Applied Biomaterials
IS - 7
ER -