In vitro and ex vivo models of adipocytes

脂肪细胞 脂肪组织 旁分泌信号 生物 体内 脂滴 细胞生物学 细胞培养 干细胞 电池类型 离体 脂肪生成 细胞分化 白色脂肪组织 内科学 内分泌学 细胞 基因 遗传学 医学 受体
作者
Jérémy Dufau,Joanne X. Shen,Morgane Couchet,Thaís de Castro Barbosa,Niklas Mejhert,Lucas Massier,Elena Griseti,Étienne Mouisel,Ez‐Zoubir Amri,Volker M. Lauschke,Mikael Rydén,Dominique Langin
出处
期刊:American Journal of Physiology-cell Physiology [American Physical Society]
卷期号:320 (5): C822-C841 被引量:133
标识
DOI:10.1152/ajpcell.00519.2020
摘要

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.
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