Tissue engineered models of adipose tissue dysfunction to investigate obesity-related comorbidities.

IF 7.7 Q1 ENGINEERING, BIOMEDICAL
Lara Ece Celebi, Frank Ketchum, Dila Naz Bozkaya, Pinar Zorlutuna
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引用次数: 0

Abstract

Emerging evidence suggests that adipose tissue is not just a fat depot but a metabolically active organ that plays a central role in connecting obesity with its comorbidities. Understanding the complex interactions between adipocytes and neighboring cell types in obesity requires models that accurately replicate adipocyte behavior within their natural environment. Three-dimensional (3D) adipocyte cultures mimic the native tissue microenvironment by incorporating the spatial architecture as well as cell-cell and cell-extracellular matrix interactions presentin vivo, offering improved platforms for (patho)physiological adipose tissue modeling. 3D models of adipose tissue dysfunction enable the study of complex cellular crosstalk, such as adipocyte cancer cell interactions in breast, colorectal, bone, and pancreatic cancers; epicardial and pericardial adipocyte-myocardial cell dynamics in obesity-related cardiac dysfunction; and adipocyte-hepatocyte interactions in the development of non-alcoholic fatty liver disease, among other critical pathophysiological processes. In this review, we first discuss 3D models of adipose tissue and current strategies for mimicking the obesogenic microenvironment, including dietary stimulation of hyperlipidemia and hyperglycemia, as well as the incorporation of oxygen gradients, proinflammatory cytokines, and immune cells. Secondly, we examine 3D co-culture platforms that incorporate disease-associated/dysfunctional adipocytes with various cell types, such as cancer cells, cardiac cells, hepatocytes, immune cells, endothelial cells (EC), and fibroblasts, to model intercellular and interorgan crosstalk in obesity. Lastly, we provide insights into enhancing the physiological relevance of dysfunctional adipose tissue models and their co-culture systems while discussing future directions in tissue engineering aimed at improving clinical translation and reducing obesity related complications and mortality.

脂肪组织功能障碍的组织工程模型研究肥胖相关的合并症。
新出现的证据表明,脂肪组织不仅是脂肪储存库,而且是代谢活跃的器官,在肥胖及其合并症之间起着核心作用。要理解肥胖中脂肪细胞和邻近细胞类型之间复杂的相互作用,需要能够在自然环境中准确复制脂肪细胞行为的模型。三维(3D)脂肪细胞培养通过结合体内存在的空间结构以及细胞-细胞和细胞-细胞外基质(ECM)相互作用来模拟天然组织微环境,为(病理)生理脂肪组织建模提供了改进的平台。脂肪组织功能障碍的3D模型能够研究复杂的细胞串扰,例如乳腺癌、结直肠癌、骨癌和胰腺癌中的脂肪细胞癌细胞相互作用;肥胖相关性心功能障碍的心外膜和心包脂肪细胞-心肌细胞动力学以及脂肪细胞-肝细胞相互作用在非酒精性脂肪肝疾病发展中的作用,以及其他关键的病理生理过程。在这篇综述中,我们首先讨论了脂肪组织的3D模型和目前模拟肥胖微环境的策略,包括饮食刺激高脂血症和高血糖症,以及氧梯度、促炎细胞因子和免疫细胞的结合。其次,我们研究了将疾病相关/功能失调脂肪细胞与各种细胞类型(如癌细胞、心肌细胞、肝细胞、免疫细胞、内皮细胞和成纤维细胞)结合在一起的3D共培养平台,以模拟肥胖中的细胞间和器官间串音。最后,我们提供了增强功能失调脂肪组织模型及其共培养系统的生理相关性的见解,同时讨论了旨在改善临床翻译和减少肥胖相关并发症和死亡率的组织工程的未来方向。
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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CiteScore
9.40
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