壳聚糖
体内
体外
材料科学
巨噬细胞极化
生物材料
生物医学工程
炎症
巨噬细胞
植入
生物物理学
细胞生物学
免疫学
纳米技术
生物
医学
生物化学
外科
生物技术
作者
Ysander von Boxberg,Sylvia Soares,Camille Giraudon,Laurent David,Maud Viallon,Alexandra Montembault,Fatiha Nothias
摘要
Abstract We have previously shown that implantation of a fragmented chitosan hydrogel suspension (chitosan‐FPHS) into a traumatic spinal cord lesion in adult rats led to significant axon regrowth and functional recovery, which was associated to a modulation of inflammation. Using an in vitro culture system, we show here that polarization of bone marrow‐derived macrophages is indeed modified by direct contact with chitosan‐FPHS. Reducing the degree of acetylation (DA) and raising the concentration of chitosan (Cp, from 1.5% to 3%), favors macrophage polarization toward anti‐inflammatory subtypes. These latter also migrate and adhere efficiently on low, but not high DA chitosan‐FPHS, both in vitro and in vivo, while inflammatory macrophages rarely invade a chitosan‐FPHS implant in vivo, no matter the DA. Our in vitro model setup should prove a valuable tool for screening diverse biomaterial formulations and combinations thereof for their inflammatory potential prior to implantation in vivo.
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