用于组织再生的蚕丝纤维素和蚕丝纤维素/纳米羟基磷灰石支架的体外巨噬细胞反应研究

IF 5.4 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Biomaterials Science & Engineering Pub Date : 2024-11-11 Epub Date: 2024-10-09 DOI:10.1021/acsbiomaterials.4c00976
Kallista Wong, Xuan Hao Tan, Jun Li, James Hoi Po Hui, James Cho Hong Goh
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引用次数: 0

摘要

近年来,由于蚕丝纤维素(SF)的机械强度和纳米羟基磷灰石(nHA)的骨诱导特性,蚕丝纤维素(SF)与低结晶度的纳米羟基磷灰石(nHA)被用作支架,用于各种组织再生应用。然而,目前对 SF 与 nHA 复合材料植入后降解产物的免疫反应还缺乏了解。众所周知,生物材料降解产生的微粒碎片会引发免疫反应。由于支架由可降解材料制成,降解产物可能会导致炎症。因此,在本研究中,与对照 SF 支架相比,研究了 SF/nHA 支架的酶降解对巨噬细胞反应的影响。由于支架的降解产物可影响巨噬细胞的极化,因此可以假设,在体外使用蛋白酶 XIV 溶液降解 SF 和 SF/nHA 支架时,降解产物可促使 THP-1 衍生巨噬细胞从促炎 M1 表型极化为抗炎 M2 表型。结果表明,SF/nHA 支架的初始降解产物(第 1 天)会引起促炎反应,而 SF/nHA 支架的后期降解产物(第 24 天)则会引起抗炎反应。此外,由于 SF 支架降解速度较快,且降解溶液中氨基酸浓度较高,因此 SF 支架的降解产物可引起较高的抗炎反应。因此,本文有助于阐明 SF 和 SF/nHA 支架的降解产物对巨噬细胞反应的促进作用,并为设计具有可调降解率的丝基生物材料提供更深入的见解,从而调节巨噬细胞的反应,用于未来的组织再生应用。
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An In Vitro Macrophage Response Study of Silk Fibroin and Silk Fibroin/Nano-Hydroxyapatite Scaffolds for Tissue Regeneration Application.

In recent years, silk fibroin (SF) has been incorporated with low crystallinity nanohydroxyapatite (nHA) as a scaffold for various tissue regeneration applications due to the mechanical strength of SF and osteoconductive properties of nHA. However, currently, there is a lack of understanding of the immune response toward the degradation products of SF with nHA composite after implantation. It is known that particulate fragments from the degradation of a biomaterial can trigger an immune response. As the scaffold is made of degradable materials, the degradation products may contribute to the inflammation. Therefore, in this study, the effects of the enzymatic degradation of the SF/nHA scaffold on macrophage response were investigated in comparison to the control SF scaffold. Since the degradation products of a scaffold can influence macrophage polarization, it can be hypothesized that as the SF and SF/nHA scaffolds were degraded in vitro using protease XIV solution, the degradation products can contribute to the polarization of THP-1-derived macrophages from pro-inflammatory M1 to anti-inflammatory M2 phenotype. The results demonstrated that the initial (day 1) degradation products of the SF/nHA scaffold elicited a pro-inflammatory response, while the latter (day 24) degradation products of the SF/nHA scaffold elicited an anti-inflammatory response. Moreover, the degradation products from the SF scaffold elicited a higher anti-inflammatory response due to the faster degradation of the SF scaffold and a higher amino acid concentration in the degradation solution. Hence, this paper can help elucidate the contributory effects of the degradation products of SF and SF/nHA scaffolds on macrophage response and provide greater insights into designing silk-based biomaterials with tunable degradation rates that can modulate macrophage response for future tissue regeneration applications.

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来源期刊
ACS Biomaterials Science & Engineering
ACS Biomaterials Science & Engineering Materials Science-Biomaterials
CiteScore
10.30
自引率
3.40%
发文量
413
期刊介绍: ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics: Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture
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