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羟基磷灰石颗粒的形状和大小通过在胶原-羟基磷灰石支架中引导巨噬细胞表型来影响间充质干细胞的成骨作用。

Hydroxyapatite Particle Shape and Size Influence MSC Osteogenesis by Directing the Macrophage Phenotype in Collagen-Hydroxyapatite Scaffolds.

作者信息

Sridharan Rukmani, Genoud Katelyn J, Kelly Daniel J, O'Brien Fergal J

机构信息

Tissue Engineering Research Group, Department of Anatomy and Regenerative Medicine, Royal College of Surgeons in Ireland, Dublin 2 D02 YN77, Ireland.

Trinity Centre for Biomedical Engineering, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2 D02 PN40, Ireland.

出版信息

ACS Appl Bio Mater. 2020 Nov 16;3(11):7562-7574. doi: 10.1021/acsabm.0c00801. Epub 2020 Oct 23.

Abstract

The field of bone tissue engineering has seen the advancement of a variety of biomaterials with a diverse range of material properties. Biomaterial properties such as particle shape and size, stiffness, and pore size all influence the osteogenic capacity of biomaterials, typically evaluated by analyzing their potential to promote osteogenesis in mesenchymal stem cells (MSCs). There is now accumulating evidence highlighting the role of macrophages in driving bone regeneration responses. In this study, we evaluated the osteogenic capacity of collagen scaffolds functionalized with hydroxyapatite particles of varying shapes (needle vs spherical) and sizes (5 μm vs 100 μm) using an culture system of MSCs alone and in coculture with macrophages. We show that macrophage response to HA particles was elevated in the presence of a scaffold with 5 μm needle-shaped particles (Coll N), with an increase in the expression and secretion of both pro-inflammatory (TNFα, IL6, and MIP1α) and anti-inflammatory (IL10 and IL1Ra) factors. When MSCs alone were cultured on the scaffolds, we show that scaffolds with HA particles were highly osteogenic, with superior osteogenesis observed in scaffolds with large 30 μm spherical particles (Coll S) compared to small 5 μm needle-shaped particles (Coll N). A coculture of MSCs with macrophages increased osteogenesis in all groups, with the most dramatic increase on Coll N scaffolds, leading to an elimination of the differences observed during monoculture. Through gene expression analysis, we showed that this correlated with an enhanced pro-osteogenic macrophage phenotype on Coll N scaffolds. These results highlight the potential of modulating material properties such as particle shape and size to develop osteoimmunomodulatory materials that direct osteogenic responses by influencing macrophage response.

摘要

骨组织工程领域已经见证了具有各种材料特性的多种生物材料的发展。生物材料的特性,如颗粒形状和大小、硬度以及孔径,都会影响生物材料的成骨能力,通常通过分析它们促进间充质干细胞(MSC)成骨的潜力来评估。现在有越来越多的证据强调巨噬细胞在驱动骨再生反应中的作用。在本研究中,我们使用单独培养的MSC以及与巨噬细胞共培养的体系,评估了用不同形状(针状与球形)和大小(5μm与100μm)的羟基磷灰石颗粒功能化的胶原支架的成骨能力。我们发现,在存在5μm针状颗粒的支架(Coll N)时,巨噬细胞对HA颗粒的反应增强,促炎因子(TNFα、IL6和MIP1α)和抗炎因子(IL10和IL1Ra)的表达和分泌均增加。当单独将MSC培养在支架上时,我们发现带有HA颗粒的支架具有高度成骨能力,与5μm小针状颗粒的支架(Coll N)相比,在30μm大球形颗粒的支架(Coll S)中观察到更好的成骨效果。MSC与巨噬细胞的共培养增加了所有组的成骨作用,在Coll N支架上增加最为显著,导致消除了单培养期间观察到的差异。通过基因表达分析,我们表明这与Coll N支架上增强的促骨生成巨噬细胞表型相关。这些结果突出了调节颗粒形状和大小等材料特性以开发通过影响巨噬细胞反应来指导成骨反应的骨免疫调节材料的潜力。

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