Human Bone Marrow Is Comprised of Adipocytes with Specific Lipid Metabolism.


Journal

Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691

Informations de publication

Date de publication:
28 01 2020
Historique:
received: 01 08 2019
revised: 19 11 2019
accepted: 24 12 2019
entrez: 30 1 2020
pubmed: 30 1 2020
medline: 21 10 2020
Statut: ppublish

Résumé

Under caloric restriction, bone marrow adipocytes (BM-Ads) do not decrease in size compared to white adipocytes, suggesting they harbor unique metabolic properties. We compare human primary BM-Ads with paired subcutaneous adipocytes (SC-Ads) using proteomic and lipidomic approaches. We find that, although SC-Ads and BM-Ads share similar morphological features, they possess distinct lipid metabolism. Although BM-Ad shows enrichment in proteins involved in cholesterol metabolism, correlating with increased free cholesterol content, proteins involved in lipolysis were downregulated. In particular, monoacylglycerol lipase expression is strongly reduced in BM-Ads, leading to monoacylglycerol accumulation. Consequently, basal and induced lipolytic responses are absent in BM-Ads, affirming their differences in metabolic fitness upon caloric restriction. These specific metabolic features are not recapitulated in vitro using common protocols to differentiate bone marrow mesenchymal stem cells. Thus, contrary to classical SC-Ads, BM-Ads display a specific lipid metabolism, as they are devoid of lipolytic activity and exhibit a cholesterol-orientated metabolism.

Identifiants

pubmed: 31995765
pii: S2211-1247(19)31754-1
doi: 10.1016/j.celrep.2019.12.089
pii:
doi:

Substances chimiques

Proteome 0
Cholesterol 97C5T2UQ7J
Monoacylglycerol Lipases EC 3.1.1.23

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

949-958.e6

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Interests The authors declare no competing interests.

Auteurs

Camille Attané (C)

Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, UPS, Toulouse, France. Electronic address: camille.attane@ipbs.fr.

David Estève (D)

Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, UPS, Toulouse, France.

Karima Chaoui (K)

Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, UPS, Toulouse, France.

Jason S Iacovoni (JS)

Plateau de Bioinformatiques, Institut des Maladies Métaboliques et Cardiovasculaires (I2MC), Université de Toulouse, INSERM, UPS, Toulouse, France.

Jill Corre (J)

Centre de Recherches en Cancérologie de Toulouse (CRCT), Université de Toulouse, INSERM, UPS, Toulouse, France.

Mohamed Moutahir (M)

Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, UPS, Toulouse, France.

Philippe Valet (P)

Institut des Maladies Métaboliques et Cardiovasculaires (I2MC), Université de Toulouse, INSERM, UPS, Toulouse, France.

Odile Schiltz (O)

Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, UPS, Toulouse, France.

Nicolas Reina (N)

Département de Chirurgie Orthopédique et Traumatologique, Hôpital Pierre-Paul Riquet, CHU de Toulouse, Toulouse, France; Laboratoire AMIS, UMR 5288 CNRS, Université Toulouse III-Paul Sabatier, Toulouse, France.

Catherine Muller (C)

Institut de Pharmacologie et de Biologie Structurale (IPBS), Université de Toulouse, CNRS, UPS, Toulouse, France. Electronic address: muller@ipbs.fr.

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Classifications MeSH