在负载AuNPs/CdSe/ tanps的PLCL/ vpp基静电纺纳米纤维存在下内皮层的形成。

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Frontiers in Molecular Biosciences Pub Date : 2025-08-18 eCollection Date: 2025-01-01 DOI:10.3389/fmolb.2025.1638442
Magdalena Lasak, Viraj P Nirwan, Dorota Kuc-Ciepluch, Ryszard Tomasiuk, Igor Chourpa, Amir Fahmi, Karol Ciepluch
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引用次数: 0

摘要

背景:静电纺丝纳米纤维可以直接或间接地影响内皮层的性质和形成,在生物医学领域得到越来越广泛的应用。这种作用可能是有毒的,也可能是促刺激的。因此,在本研究中,研究了由可生物降解和生物相容性好的l -丙交酯嵌段-ϵ-caprolactone共聚物(PLCL, 70:30)与聚乙烯吡罗烷酮(PVP)共混而成的电纺丝纳米纤维PLCL/PVP,其中含有原位合成的PVP不同类型的纳米粒子-金(AuNPs)、硒化镉(CdSe QDs)或钽(TaNPs)。了解纳米纤维的不同修饰如何影响内皮层的形成对于将其作为组织再生的工具至关重要。方法:合成了含金(AuNPs)、硒化镉(CdSe)和钽(TaNPs)的静电纺丝纳米纤维,并对其进行了理化性质分析。采用显微和荧光技术研究了纳米纤维对人脐静脉内皮细胞的细胞毒性和促增殖作用。结果:内皮层在24 h后形成75%的融合,在没有纳米纤维存在的情况下,72 h后形成100%的融合。72小时后,PLCL/PVP纳米纤维的内皮层形成较慢(60%)和(80%)。在纳米纤维中引入各种纳米颗粒会改变内皮层的形态和形成速度。在AuNPs修饰的纳米纤维存在下,72 h后仅达到40%。PLCL/PVP-CdSe量子点也有类似的效果。对于PLCL/PVP-TaNPs, 48 h后为90%,72 h后为100%。测试的纳米纤维对形成的HUVEC细胞单层没有表现出毒性行为。除了PLCL/PVP-TaNPs外,所有测试的纳米纤维都诱导HUVEC细胞层通透性增加,导致荧光标记的葡聚糖转位从20%增加到50%。结论:纳米纤维对内皮层形成的影响可能是直接的,细胞与纳米纤维接触,从而阻碍内皮层的生长。此外,生物液体成分的摄取可间接影响内皮细胞的粘附和生长。在测试的纳米纤维中,无毒的PLCL/PVP-TaNPs似乎特别有前途,因为它们具有安全性问题,并且可以用作有效的支架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The endothelial layer formation in the presence of AuNPs/CdSe/TaNPs-loaded PLCL/PVP-based electrospun nanofibers.

Background: Electrospun nanofibers, which are becoming increasingly popular in biomedicine, can directly or indirectly affect the properties and formation of the edothelial layer. This effect can be both toxic and pro-stimulatory. Therefore, in this study, electrospun nanofibers PLCL/PVP composed of biodegradable and biocompatible L-lactide-block-ϵ-caprolactone copolymer (PLCL, 70:30) blended with polyvinylpyrrolidone (PVP), containing in situ synthesized PVP different types of nanoparticles - gold (AuNPs), cadmium selenide (CdSe QDs) or tantalum (TaNPs), were investigated. Understanding how different modifications of nanofibers can affect the formation of the endothelial layer is crucial to using them as tools in tissue regeneration.

Methods: electrospun nanofibers with gold (AuNPs), cadmium selenide (CdSe QDs) or tantalum (TaNPs), were synthesized and physico-chemical characteristic were caried out. Cytotoxicity and prostimulatory effect of nanofibers on Primary Human Umbilical Vein Endothelial Cells were tested by microscopic and spectrofluorescence techniques.

Results: The endothelial layer forms to 75% confluence (after 24 h) and reaches 100% after 72 h when no nanofibers are present. A slower formation of the endothelial layer is seen in the presence of PLCL/PVP nanofibers (60%) and (80%) after 72 h. The introduction of various nanoparticles into the nanofibers caused changes in the morphology and rate of endothelial layer formation. In the presence of nanofibers modified with AuNPs after 72 h it reached only 40%. A similar effect was obtained for PLCL/PVP-CdSe QDs. In the case of PLCL/PVP-TaNPs, after 48 h 90% and after 72 h 100%. The tested nanofibers did not show toxic behavior towards the formed HUVEC cell monolayer. All of the tested nanofibers, except PLCL/PVP-TaNPs, induced increased HUVEC cells layer permeability, which resulted in increased translocation of fluorescently labeled dextran from 20% to 50%.

Conclusion: It was estimated that the effect of nanofibers on the formation of the endothelial layer can be direct, where cells contact the nanofibers and thus the growth of the endothelium is hindered. Additionally, the uptake of biological fluid components can have an indirect effect on endothelial cells, their adhesion and growth. Among the tested nanofibers, non-toxic PLCL/PVP-TaNPs seem to be particularly promising due to safety issues and the possibility of using them as effective scaffolds.

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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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