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一种新型的人类原代乳腺脂肪细胞 3D 培养模型,用于研究在肥胖和消瘦状态下它们与乳腺癌的代谢串扰。

A novel 3D culture model for human primary mammary adipocytes to study their metabolic crosstalk with breast cancer in lean and obese conditions.

机构信息

Institut de Pharmacologie et de Biologie Structurale, CNRS/Université de Toulouse UMR 5089, 205 route de Narbonne, BP 64182, 31077, Toulouse, France.

Département de Chirurgie Gynécologique oncologique, CHU-Toulouse, Institut Universitaire du Cancer de Toulouse-Oncopole, 1 avenue Irène Joliot-Curie, 31059, Toulouse Cedex 9, France.

出版信息

Sci Rep. 2023 Mar 22;13(1):4707. doi: 10.1038/s41598-023-31673-x.

Abstract

Obesity is a negative prognosis factor for breast cancer. Yet, the biological mechanisms underlying this effect are still largely unknown. An emerging hypothesis is that the transfer of free fatty acids (FFA) between adipocytes and tumor cells might be altered under obese conditions, contributing to tumor progression. Currently there is a paucity of models to study human mammary adipocytes (M-Ads)-cancer crosstalk. As for other types of isolated white adipocytes, herein, we showed that human M-Ads die within 2-3 days by necrosis when grown in 2D. As an alternative, M-Ads were grown in a fibrin matrix, a 3D model that preserve their distribution, integrity and metabolic function for up to 5 days at physiological glucose concentrations (5 mM). Higher glucose concentrations frequently used in in vitro models promote lipogenesis during M-Ads culture, impairing their lipolytic function. Using transwell inserts, the matrix embedded adipocytes were cocultured with breast cancer cells. FFA transfer between M-Ads and cancer cells was observed, and this event was amplified by obesity. Together these data show that our 3D model is a new tool for studying the effect of M-Ads on tumor cells and beyond with all the components of the tumor microenvironment including the immune cells.

摘要

肥胖是乳腺癌的一个负面预后因素。然而,这种影响的生物学机制在很大程度上仍不清楚。一个新兴的假设是,在肥胖情况下,脂肪细胞和肿瘤细胞之间游离脂肪酸 (FFA) 的转移可能会发生改变,从而促进肿瘤的进展。目前,缺乏研究人类乳腺脂肪细胞 (M-Ads)-肿瘤相互作用的模型。与其他类型的分离的白色脂肪细胞不同,在这里,我们显示当在 2D 中生长时,人 M-Ads 在 2-3 天内通过坏死死亡。作为替代方案,M-Ads 在纤维蛋白基质中生长,这是一种 3D 模型,可在生理葡萄糖浓度(5mM)下将其分布、完整性和代谢功能保持长达 5 天。在体外模型中经常使用的较高葡萄糖浓度会促进 M-Ads 培养期间的脂肪生成,从而损害其脂肪分解功能。使用 Transwell 插入物,基质包埋的脂肪细胞与乳腺癌细胞共培养。观察到 M-Ads 和癌细胞之间的 FFA 转移,并且肥胖会放大这种转移。这些数据表明,我们的 3D 模型是研究 M-Ads 对肿瘤细胞影响的新工具,并且可以研究肿瘤微环境的所有成分,包括免疫细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b09a/10033714/a56f0cc97ded/41598_2023_31673_Fig1_HTML.jpg

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