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电纺纤维表面粗糙度调节人单核细胞衍生巨噬细胞表型。

Electrospun Fiber Surface Roughness Modulates Human Monocyte-Derived Macrophage Phenotype.

作者信息

Alemifar Aidan, Burnette KaLia, Jandres Bryan, Hurt Samuel, Tse Hubert M, Robinson Jennifer L

机构信息

Department of Orthopaedic Surgery and Sports Medicine, University of Washington.

Bioengineering Graduate Program, University of Kansas.

出版信息

bioRxiv. 2024 Sep 3:2024.08.30.610568. doi: 10.1101/2024.08.30.610568.

DOI:10.1101/2024.08.30.610568
PMID:39282362
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11398424/
Abstract

Injuries to fibrous connective tissues have very little capacity for self-renewal and exhibit poor healing after injury. Phenotypic shifts in macrophages play a vital role in mediating the healing response, creating an opportunity to design immunomodulatory biomaterials which control macrophage polarization and promote regeneration. In this study, electrospun poly(-caprolactone) fibers with increasing surface roughness (SR) were produced by increasing relative humidity and inducing vapor-induced phase separation during the electrospinning process. The impact of surface roughness on macrophage phenotype was assessed using human monocyte-derived macrophages and using B6.Cg-Tg(Csf1r-EGFP)1Hume/J (MacGreen) mice. experiments showed that macrophages cultured on mesh with increasing SR exhibited decreased release of both pro- and anti-inflammatory cytokines potentially driven by increased protein adsorption and biophysical impacts on the cells. Further, increasing SR led to an increase in the expression of the pro-regenerative cell surface marker CD206 relative to the pro-inflammatory marker CD80. Mesh with increasing SR were implanted subcutaneously in MacGreen mice, again showing an increase in the ratio of cells expressing CD206 to those expressing CD80 visualized by immunofluorescence. SR on implanted biomaterials is sufficient to drive macrophage polarization, demonstrating a simple feature to include in biomaterial design to control innate immunity.

摘要

纤维结缔组织损伤后的自我更新能力非常有限,损伤后愈合不良。巨噬细胞的表型转变在介导愈合反应中起着至关重要的作用,这为设计能够控制巨噬细胞极化并促进再生的免疫调节生物材料创造了机会。在本研究中,通过在静电纺丝过程中提高相对湿度并诱导气相诱导相分离,制备了表面粗糙度(SR)不断增加的静电纺聚己内酯纤维。使用人单核细胞衍生的巨噬细胞和B6.Cg-Tg(Csf1r-EGFP)1Hume/J(MacGreen)小鼠评估表面粗糙度对巨噬细胞表型的影响。实验表明,在SR不断增加的网片上培养的巨噬细胞,其促炎和抗炎细胞因子的释放均减少,这可能是由蛋白质吸附增加和对细胞的生物物理影响所驱动的。此外,相对于促炎标记物CD80,SR的增加导致促再生细胞表面标记物CD206的表达增加。将SR不断增加的网片皮下植入MacGreen小鼠体内,通过免疫荧光观察再次显示,表达CD206的细胞与表达CD80的细胞的比例增加。植入生物材料上的SR足以驱动巨噬细胞极化,这表明在生物材料设计中纳入一个简单的特征来控制先天免疫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/4c6e59d73424/nihpp-2024.08.30.610568v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/57b7d230a6b5/nihpp-2024.08.30.610568v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/a86d40cdb61a/nihpp-2024.08.30.610568v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/43ca51228880/nihpp-2024.08.30.610568v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/5fd93960acbb/nihpp-2024.08.30.610568v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/b46a2a0d7be4/nihpp-2024.08.30.610568v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/4c6e59d73424/nihpp-2024.08.30.610568v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/57b7d230a6b5/nihpp-2024.08.30.610568v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/a86d40cdb61a/nihpp-2024.08.30.610568v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/43ca51228880/nihpp-2024.08.30.610568v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/5fd93960acbb/nihpp-2024.08.30.610568v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/b46a2a0d7be4/nihpp-2024.08.30.610568v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/11398424/4c6e59d73424/nihpp-2024.08.30.610568v1-f0007.jpg

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