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体外和离体脂肪细胞模型。

In vitro and ex vivo models of adipocytes.

机构信息

Inserm, Institute of Metabolic and Cardiovascular Diseases (I2MC), UMR1297, Toulouse, France.

Faculté de Médecine, I2MC, UMR1297, Université de Toulouse, Université Paul Sabatier, Toulouse, France.

出版信息

Am J Physiol Cell Physiol. 2021 May 1;320(5):C822-C841. doi: 10.1152/ajpcell.00519.2020. Epub 2021 Jan 13.

DOI:10.1152/ajpcell.00519.2020
PMID:33439778
Abstract

Adipocytes are specialized cells with pleiotropic roles in physiology and pathology. Several types of fat cells with distinct metabolic properties coexist in various anatomically defined fat depots in mammals. White, beige, and brown adipocytes differ in their handling of lipids and thermogenic capacity, promoting differences in size and morphology. Moreover, adipocytes release lipids and proteins with paracrine and endocrine functions. The intrinsic properties of adipocytes pose specific challenges in culture. Mature adipocytes float in suspension culture due to high triacylglycerol content and are fragile. Moreover, a fully differentiated state, notably acquirement of the unilocular lipid droplet of white adipocyte, has so far not been reached in two-dimensional culture. Cultures of mouse and human-differentiated preadipocyte cell lines and primary cells have been established to mimic white, beige, and brown adipocytes. Here, we survey various models of differentiated preadipocyte cells and primary mature adipocyte survival describing main characteristics, culture conditions, advantages, and limitations. An important development is the advent of three-dimensional culture, notably of adipose spheroids that recapitulate in vivo adipocyte function and morphology in fat depots. Challenges for the future include isolation and culture of adipose-derived stem cells from different anatomic location in animal models and humans differing in sex, age, fat mass, and pathophysiological conditions. Further understanding of fat cell physiology and dysfunction will be achieved through genetic manipulation, notably CRISPR-mediated gene editing. Capturing adipocyte heterogeneity at the single-cell level within a single fat depot will be key to understanding diversities in cardiometabolic parameters among lean and obese individuals.

摘要

脂肪细胞是具有多种生理和病理作用的特化细胞。在哺乳动物的各种解剖定义的脂肪组织中,存在着具有不同代谢特性的几种脂肪细胞。白色、米色和棕色脂肪细胞在处理脂质和产热能力方面存在差异,促进了它们在大小和形态上的差异。此外,脂肪细胞释放具有旁分泌和内分泌功能的脂质和蛋白质。脂肪细胞的内在特性在培养中带来了特殊的挑战。成熟脂肪细胞由于三酰基甘油含量高而在悬浮培养中漂浮,并且很脆弱。此外,在二维培养中,尚未达到完全分化状态,特别是白色脂肪细胞的单室脂质滴的获得。已经建立了小鼠和人分化前体脂肪细胞系和原代细胞的培养,以模拟白色、米色和棕色脂肪细胞。在这里,我们调查了各种分化前体脂肪细胞和原代成熟脂肪细胞的存活模型,描述了它们的主要特征、培养条件、优点和局限性。一个重要的发展是三维培养的出现,特别是脂肪球体的培养,这些球体在脂肪组织中再现了体内脂肪细胞的功能和形态。未来的挑战包括从不同解剖位置分离和培养动物模型和人类中的脂肪干细胞,这些细胞在性别、年龄、脂肪量和病理生理条件方面存在差异。通过基因操作,特别是 CRISPR 介导的基因编辑,进一步了解脂肪细胞的生理和功能障碍,将有助于实现这一目标。在单个脂肪组织中捕获脂肪细胞的单细胞异质性将是理解瘦人和肥胖个体中心血管代谢参数多样性的关键。

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