Collagen microgel to simulate the adipocyte microenvironment for in vitro research on obesity.

IF 1.5 4区 生物学 Q4 CELL BIOLOGY
Natalia Moreno-Castellanos, Elías Cuartas-Gómez, Oscar Vargas-Ceballos
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引用次数: 0

Abstract

Obesity is linked to adipose tissue dysfunction, a dynamic endocrine organ. Two-dimensional cultures present technical hurdles hampering their ability to follow individual or cell groups for metabolic disease research. Three-dimensional type I collagen microgels with embedded adipocytes have not been thoroughly investigated to evaluate adipogenic maintenance as instrument for studying metabolic disorders. We aimed to develop a novel tunable Col-I microgel simulating the adipocyte microenvironment to maintain differentiated cells with only insulin as in vitro model for obesity research. Adipocytes were cultured and encapsulated in collagen microgels at different concentrations (2, 3 and 4 mg/mL). Collagen microgels at 3 and 4 mg/mL were more stable after 8 days of culture. However, cell viability and metabolic activity were maintained at 2 and 3 mg/mL, respectively. Cell morphology, lipid mobilization and adipogenic gene expression demonstrated the maintenance of adipocyte phenotype in an in vitro microenvironment. We demonstrated the adequate stability and biocompatibility of the collagen microgel at 3 mg/mL. Cell and molecular analysis confirmed that adipocyte phenotype is maintained over time in the absence of adipogenic factors. These findings will help better understand and open new avenues for research on adipocyte metabolism and obesity. Insight box In the context of adipose tissue dysfunction research, new struggles have arisen owing to the difficulty of cellular maintenance in 2D cultures. Herein, we sought a novel approach using a 3D type I collagen-based biomaterial to adipocyte culture with only insulin. This component was tailored as a microgel in different concentrations to support the growth and survival of adipocytes. We demonstrate that adipocyte phenotype is maintained and key adipogenesis regulators and markers are over time. The cumulative results unveil the practical advantage of this microgel platform as an in vitro model to study adipocyte dysfunction and obesity.

胶原微凝胶模拟脂肪细胞微环境用于肥胖的体外研究。
肥胖与脂肪组织功能障碍有关,脂肪组织是一种动态内分泌器官。二维培养存在技术障碍,阻碍了它们追踪个体或细胞群进行代谢疾病研究的能力。嵌入脂肪细胞的三维I型胶原微凝胶尚未被充分研究,以评估脂肪形成维持作为研究代谢紊乱的工具。我们旨在开发一种新型的可调col - 1微凝胶,模拟脂肪细胞微环境,以维持仅用胰岛素的分化细胞作为肥胖研究的体外模型。将脂肪细胞培养并包被不同浓度(2、3、4 mg/mL)的胶原微凝胶。3和4 mg/mL的胶原微凝胶在培养8天后更加稳定。然而,在2和3 mg/mL浓度下,细胞活力和代谢活性保持不变。细胞形态、脂质动员和脂肪生成基因表达证明了脂肪细胞表型在体外微环境中的维持。我们证明了胶原微凝胶在3mg /mL时具有足够的稳定性和生物相容性。细胞和分子分析证实,脂肪细胞表型在缺乏脂肪形成因素的情况下维持一段时间。这些发现将有助于更好地理解并为脂肪细胞代谢和肥胖的研究开辟新的途径。在脂肪组织功能障碍研究的背景下,由于二维培养中细胞维持的困难,新的斗争已经出现。在此,我们寻求一种使用3D I型胶原基生物材料进行仅胰岛素脂肪细胞培养的新方法。该成分被定制为不同浓度的微凝胶,以支持脂肪细胞的生长和存活。我们证明脂肪细胞表型是维持的,关键的脂肪生成调节因子和标记是随时间变化的。累积的结果揭示了这种微凝胶平台作为研究脂肪细胞功能障碍和肥胖的体外模型的实际优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Integrative Biology
Integrative Biology 生物-细胞生物学
CiteScore
4.90
自引率
0.00%
发文量
15
审稿时长
1 months
期刊介绍: Integrative Biology publishes original biological research based on innovative experimental and theoretical methodologies that answer biological questions. The journal is multi- and inter-disciplinary, calling upon expertise and technologies from the physical sciences, engineering, computation, imaging, and mathematics to address critical questions in biological systems. Research using experimental or computational quantitative technologies to characterise biological systems at the molecular, cellular, tissue and population levels is welcomed. Of particular interest are submissions contributing to quantitative understanding of how component properties at one level in the dimensional scale (nano to micro) determine system behaviour at a higher level of complexity. Studies of synthetic systems, whether used to elucidate fundamental principles of biological function or as the basis for novel applications are also of interest.
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