Macrophage activity modulation via synergistic effect of a porous substrate and low-field laser therapy.

IF 0.8 Acta of bioengineering and biomechanics Pub Date : 2025-01-28 Print Date: 2024-06-01 DOI:10.37190/abb-02451-2024-02
Aleksandra Matuła, Amelia Lizak, Ewa Stodolak-Zych, Beata Stenka, Joanna Homa, Aneta Bac, Aneta Teległów, Anna Ścisłowska-Czarnecka
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Abstract

Purpose: The aim of this study was to investigate the effect of substrate - polycaprolactone (PCL)-based porous membrane modified with rosmarinic acid (RA), (PCL-RA) and to determine the optimal values of low field laser irradiation (LLLT) as stimulators of biological response of RAW 264.7 macrophages. Methods: The porous polymer membrane was obtained by the phase inversion method, the addition of rosmarinic acid was 1%wt. The reference material was pure polymer membrane. RAW 264.7 were deposited on the material and then irradiated with a laser with a wavelength of 808 nm, a power of 100 mW, an irradiation dose of 2 J/cm2/cell well, applied continuously (C), (100/2/C) or pulsed (I), (100/2/I). Results: Macrophage irradiation resulted in an increase in their adhesion. Modifying the PCL membranes with rosmarinic acid had no effect on cell viability on day 3 of the cell culture. Irradiation of macrophages cultured on PCL-RA material increased their viability. Irradiation of macrophages cultured on PCL-RA material decreased macrophage secretion of NO and protein and the increase in TNF and MCP-1 secretion was only transient on day 3 of culture. Conclusions: Macrophage irradiation had a positive effect on macrophage attachment. Modification of PCL membranes with rosmarinic acid influenced the biological activity of macrophages. Culture of macrophages on rosmarinic acid-modified PCL membranes and simultaneous irradiation of LLLT cells resulted in anti-inflammatory effects.

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通过多孔基质和低场激光治疗的协同作用调节巨噬细胞活性。
目的:研究迷迭香酸修饰的底物-聚己内酯(PCL)基多孔膜(PCL-RA)对raw264.7巨噬细胞生物反应的影响,并确定低场激光照射(LLLT)的最佳刺激值。方法:采用相转化法制备多孔聚合物膜,迷迭香酸添加量为1%wt。标准物质为纯高分子膜。将RAW 264.7沉积在材料上,然后用波长为808 nm,功率为100 mW,照射剂量为2 J/cm2/cell well的激光照射,连续(C), (100/2/C)或脉冲(I), (100/2/I)。结果:巨噬细胞照射使其黏附增强。用迷迭香酸修饰PCL膜对细胞培养第3天的细胞活力没有影响。在PCL-RA材料上培养的巨噬细胞辐照后,其活力增加。在PCL-RA材料上培养的巨噬细胞辐照后,巨噬细胞NO和蛋白质的分泌减少,TNF和MCP-1分泌的增加在培养第3天只是短暂的。结论:巨噬细胞辐照对巨噬细胞粘附有积极作用。迷迭香酸修饰PCL膜影响巨噬细胞的生物活性。巨噬细胞在迷迭香酸修饰的PCL膜上培养,同时照射LLLT细胞,可产生抗炎作用。
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