Extending the Three-Dimensional Culture of Adipocytes Through Surface Coatings.

IF 3.8 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Sheetal Chowdhury, Komal Beeton, Zacchaeus Wallace, Maggie Moore, Gene L Bidwell, Amol V Janorkar
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引用次数: 0

Abstract

To mimic the important features of progressing adiposity, in vitro adipose cell culture models must allow gradual intracellular fat accumulation in the three-dimensional (3D) arrangement of adipose-derived stem cells (ASCs) over a long-term culture period. Previously, elastin-like polypeptide (ELP) and polyethyleneimine (PEI) have been used to culture human adipose-derived stem cells (hASCs) as 3D spheroids and to differentiate them to adipocytes over a relatively long culture period of up to 5 weeks. In this study, to further enhance the spheroid adhesion properties, ELP was fused with Arginine-Glycine-Aspartic Acid (RGD) residues, known for their role as cell-attachment sites. This study aimed to assess whether the addition of RGD to the C-or N-terminus of ELP would impact the spheroid-forming ability of ELP-PEI coatings. ELP-RGD conjugates were produced using genetically modified Escherichia coli to express ELP-(RGD)3 and (RGD)3-ELP, followed by chemical conjugation with PEI. SDS gel electrophoresis, FTIR spectroscopy, and turbidimetry analyses revealed that ELP was conjugated with RGD without much alteration in the molecular weight, functional groups present, and transition temperature of ELP. The addition of RGD to ELP also did not affect the chemical conjugation capacity of ELP to PEI. We observed that the ELP-PEI coating formed slightly larger spheroids (61.8 ± 3.2 µm) compared to the ELP-(RGD)3-PEI and (RGD)3-ELP-PEI coatings (56.6 ± 3.0 and 53.4 ± 2.4 µm, respectively). Despite the size difference, ELP-(RGD)3-PEI coatings exhibited superior spheroid retention during media changes, with minimal spheroid loss. DNA assay results confirmed a significant decrease in the DNA concentration (p < 0.05) after the 20 media changes for spheroids cultured on the ELP-PEI coating, indicating spheroid loss. However, there was no significant difference in DNA concentration before and after 20 media changes for spheroids cultured on the ELP-(RGD)3-PEI and (RGD)3-ELP-PEI coatings (p > 0.05). These findings suggest that RGD incorporation does not hinder the initial spheroid formation ability of the ELP-PEI coating and enhances spheroid retention under dynamic culture conditions.

为了模拟渐进性脂肪变性的重要特征,体外脂肪细胞培养模型必须允许脂肪来源干细胞(ASCs)在三维(3D)排列的长期培养过程中逐渐积累细胞内脂肪。在此之前,弹性蛋白样多肽(ELP)和聚乙烯亚胺(PEI)已被用于将人脂肪源性干细胞(hASCs)培养成三维球体,并在长达5周的相对较长培养期内将其分化为脂肪细胞。在本研究中,为了进一步增强球状粘附特性,ELP与精氨酸-甘氨酸-天冬氨酸(RGD)残基融合,RGD残基是众所周知的细胞粘附位点。本研究旨在评估在 ELP 的 C 端或 N 端添加 RGD 是否会影响 ELP-PEI 涂层的球形形成能力。利用转基因大肠杆菌表达 ELP-(RGD)3 和 (RGD)3-ELP 并与 PEI 化学共轭,制备出 ELP-RGD 共轭物。SDS 凝胶电泳、傅立叶变换红外光谱和浊度分析表明,ELP 与 RGD 共轭后,ELP 的分子量、存在的官能团和转变温度没有发生太大变化。在 ELP 中添加 RGD 也不会影响 ELP 与 PEI 的化学共轭能力。我们观察到,与 ELP-(RGD)3-PEI 和 (RGD)3-ELP-PEI 涂层(分别为 56.6 ± 3.0 和 53.4 ± 2.4 µm)相比,ELP-PEI 涂层形成的球体稍大(61.8 ± 3.2 µm)。尽管尺寸不同,ELP-(RGD)3-PEI 涂层在更换培养基时仍能保持较好的球形,球形丢失极少。DNA 检测结果证实,ELP-PEI 涂层上培养的球体在更换 20 次培养基后,DNA 浓度显著下降(p < 0.05),表明球体丢失。然而,在ELP-(RGD)3-PEI和(RGD)3-ELP-PEI涂层上培养的球体,DNA浓度在20次培养基变化前后没有明显差异(p > 0.05)。这些研究结果表明,RGD 的加入不会阻碍 ELP-PEI 涂层的初始球体形成能力,并能增强动态培养条件下的球体保持能力。
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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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