Literature DB >> 32466532

Lipidomic Phenotyping Reveals Extensive Lipid Remodeling during Adipogenesis in Human Adipocytes.

Florian Miehle1,2, Gabriele Möller1, Alexander Cecil1, Jutta Lintelmann1, Martin Wabitsch3, Janina Tokarz1, Jerzy Adamski1,2,4,5, Mark Haid1.   

Abstract

Differentiation of preadipocytes into mature adipocytes is a highly complex cellular process. At lipidome level, the adipogenesis remains poorly characterized. To investigate the lipidomic changes during human adipogenesis, we used the LipidyzerTM assay, which quantified 743 lipid species from 11 classes. The undifferentiated human SGBS cell strain showed a heterogeneous lipid class composition with the most abundant classes, phosphatidylethanolamines (PE), phosphatidylcholines (PC), and sphingomyelins (SM). The differentiation process was accompanied by increased ceramide concentrations. After completion of differentiation around day 4, massive lipid remodeling occurred during maturation, characterized by substantial synthesis of diacylglycerols (DAG), lysophosphatidylethanolamines (LPE), PC, PE, SM, and triacylglycerols (TAG). Lipid species composition became more homogeneous during differentiation to highly concentrated saturated and monounsaturated long-chain fatty acids (LCFA), with the four most abundant being C16:0, C16:1, C18:0, and C18:1. Simultaneously, the amount of polyunsaturated and very long-chain fatty acids (VLCFA) markedly decreased. High negative correlation coefficients between PE and PC species containing VLCFA and TAG species as well as between ceramides and SM imply that PE, PC, and ceramides might have served as additional sources for TAG and SM synthesis, respectively. These results highlight the enormous remodeling at the lipid level over several lipid classes during adipogenesis.

Entities:  

Keywords:  Simpson-Golabi-Behmel syndrome (SGBS); adipocytes; adipogenesis; differential mobility spectrometry (DMS); lipidomics; lipidyzer; mass spectrometry; metabolomics; phenotyping

Year:  2020        PMID: 32466532     DOI: 10.3390/metabo10060217

Source DB:  PubMed          Journal:  Metabolites        ISSN: 2218-1989


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