Bioengineering Institute of Technology, Universitat Internacional de Catalunya, Sant Cugat del Vallès, Barcelona, Spain.
Sci Rep. 2021 Jun 3;11(1):11707. doi: 10.1038/s41598-021-91070-0.
Biomaterials and scaffolds for Tissue Engineering are widely used for an effective healing and regeneration. However, the implantation of these scaffolds causes an innate immune response in which the macrophage polarization from M1 (pro-inflammatory) to M2 (anti-inflammatory) phenotype is crucial to avoid chronic inflammation. Recent studies have showed that the use of bioactive ions such as cobalt (Co), copper (Cu) and magnesium (Mg) could improve tissue regeneration, although there is limited evidence on their effect on the macrophage response. Therefore, we investigated the immunomodulatory potential of Co, Cu and Mg in macrophage polarization. Our results indicate that Mg and concentrations of Cu lower than 10 μM promoted the expression of M2 related genes. However, higher concentrations of Cu and Co (100 μM) stimulated pro-inflammatory marker expression, indicating a concentration dependent effect of these ions. Furthermore, Mg were able to decrease M1 marker expression in presence of a mild pro-inflammatory stimulus, showing that Mg can be used to modulate the inflammatory response, even though their application can be limited in a strong pro-inflammatory environment.
用于组织工程的生物材料和支架被广泛用于有效治疗和再生。然而,这些支架的植入会引起固有免疫反应,其中巨噬细胞从 M1(促炎)向 M2(抗炎)表型的极化对于避免慢性炎症至关重要。最近的研究表明,使用钴(Co)、铜(Cu)和镁(Mg)等生物活性离子可以促进组织再生,尽管关于它们对巨噬细胞反应的影响的证据有限。因此,我们研究了 Co、Cu 和 Mg 对巨噬细胞极化的免疫调节潜力。我们的结果表明,Mg 和浓度低于 10 μM 的 Cu 促进了 M2 相关基因的表达。然而,较高浓度的 Cu 和 Co(100 μM)刺激了促炎标志物的表达,表明这些离子具有浓度依赖性效应。此外,在轻度促炎刺激存在的情况下,Mg 能够降低 M1 标志物的表达,表明 Mg 可用于调节炎症反应,尽管在强烈的促炎环境中其应用可能会受到限制。