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Adipocyte and Cell Biology

Identification of the ectoenzyme CD38 as a marker of committed preadipocytes

Abstract

Background/Objectives:

Characterisation of the adipocyte cellular lineage is required for a better understanding of white adipose tissue homoeostasis and expansion. Although several studies have focused on the phenotype of the most immature adipocyte progenitors, very few tools exist to identify committed cells. In haematopoiesis, the CD38 ectoenzyme is largely used to delineate various stages of stem cell lineage commitment. We hypothesise that this marker could be used to identify committed preadipocytes.

Methods:

Complementary strategies including flow cytometry, cell-sorting approaches, immunohistochemistry and primary cultures of murine adipose progenitors isolated from different fat pads of control or high-fat diet exposed C57BL/6 J mice were used to determine the molecular expression profile, proliferative and differentiation potentials of adipose progenitors expressing the CD38 molecule.

Results:

We demonstrate here that a subpopulation of CD45 CD31 CD34+ adipose progenitors express the cell surface protein CD38. Using a cell-sorting approach, we found that native CD45 CD31 CD34+ CD38+ (CD38+) adipose cells expressed lower CD34 mRNA and protein levels and higher levels of adipogenic genes such as Pparg, aP2, Lpl and Cd36 than did the CD45 CD31 CD34+ CD38 (CD38) population. When cultivated, CD38+ cells displayed reduced proliferative potential, assessed by BrdU incorporation and colony-forming unit assays, and greater adipogenic potential. In vitro, both CD38 mRNA and protein levels were increased during adipogenesis and CD38 cells converted into CD38+ cells when committed to the adipogenic differentiation programme. We also found that obesity development was associated with an increase in the number of CD38+ adipose progenitors, this effect being more pronounced in intra-abdominal than in subcutaneous fat, suggesting a higher rate of adipocyte commitment in visceral depots.

Conclusions:

Together, these data demonstrate that CD38 represents a new marker that identifies committed preadipocytes as CD45 CD31 CD34low CD38+ cells.

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Acknowledgements

We thank Dr Adriouch (Faculté de Médecine et de Pharmacie, Inserm U905, Institut de Recherche et d'Innovation Biomédicale, Université de Rouen, France), Dr Lund (Charles H. McCauley Professor and Chair Department of Microbiology, University of Alabama, Birmingham, United States) and Dr Pisani and Amri (Institut de Biologie Valrose, CNRS UMR7277, Inserm U1091, UNS Université Nice Sophia Antipolis, France) for fruitful discussions. We are grateful to the I2MC/UMR1048, GeT (Génome et Transcriptome) Platform, Génopole Toulouse. We also thank Dr D'Angelo and Zanoun for assistance and advice with imaging (Cellular Imaging Facility Rangueil-I2MC/TRI Platform). The authors thank the US006/CREFRE INSERM/UPS (Toulouse, France) and specifically the zootechnical core facility for animal care and the Toulouse RIO Imaging. We thank Mrs Zakaroff-Girard and Riant (Cytometry Core Facility, Inserm U1048, part of TRI Imaging Platform, Genotoul) for cell-sorting technical assistance. We especially thank Mrs Ducos for excellent technical assistance as well as Mrs Renoud, Achard, André and Mr De Vecchi (STROMALab) for their help in experiment management. This work was supported by the European Union Framework Programme 7 projects DIABAT [grant number HEALTH-F2-2011-278373] and METABOSTEM [grant number PCIG9-GA-2011-293720].

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Correspondence to A Carrière or L Casteilla.

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Carrière, A., Jeanson, Y., Côté, JA. et al. Identification of the ectoenzyme CD38 as a marker of committed preadipocytes. Int J Obes 41, 1539–1546 (2017). https://doi.org/10.1038/ijo.2017.140

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