In vitro and ex vivo models of adipocytes

Author:

Dufau Jérémy12,Shen Joanne X.3,Couchet Morgane4,De Castro Barbosa Thais4,Mejhert Niklas4,Massier Lucas4,Griseti Elena12,Mouisel Etienne12,Amri Ez-Zoubir5,Lauschke Volker M.3,Rydén Mikael4,Langin Dominique126ORCID

Affiliation:

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

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

3. Karolinska Institutet, Department of Physiology and Pharmacology, Stockholm, Sweden

4. Karolinska Institutet, Department of Medicine (H7), Stockholm, Sweden

5. Université Côte d’Azur, CNRS, Inserm, iBV, Nice, France

6. Toulouse University Hospitals, Department of Biochemistry, Toulouse, France

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.

Funder

EC | European Research Council

Fondation pour la Recherche Médicale

Agence Nationale de la Recherche

Publisher

American Physiological Society

Subject

Cell Biology,Physiology

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