A simple method for quantifying de novo lipogenesis rate and substrate selection in cell cultures by 13 C NMR isotopomer analysis of the crude lipid fraction

• Published in: NMR in biomedicine Vol. 35; no. 3; p. e4648
• Main Authors: Patrício, João S., Dias‐Pedroso, Daniela, Carvalho, Rui A., Viera, Helena L. A., Jones, John G.
• Format: Journal Article
• Language: English
• Published: England 01.03.2022
• Subjects: Acetyl Coenzyme A - metabolism; Animals; Carbon-13 Magnetic Resonance Spectroscopy - methods; Cells, Cultured; Glucose - metabolism; Lipogenesis; Mice; Microglia - metabolism; lipogenesis; fatty acids; 13C-isotopomer; microglia
• ISSN: 0952-3480; 1099-1492; 1099-1492
• DOI: 10.1002/nbm.4648

De novo lipogenesis (DNL) is critical for cell growth and maintenance, and acetyl-CoA precursors can be derived from different substrates. We developed a C NMR analysis of lipid extracts from cultured microglia cells administered with [U- C]glucose that informs overall lipogenic activity as well as the contribution of glucose to lipogenic acetyl-CoA. BV-2 microglial cell line cultured with glucose and glutamine was provided with [U- C]glucose and unlabeled glutamine for 24 h and studied in either the presence or absence of lipopolysaccharide (LPS). Cells were then extracted for lipids and the crude lipid fraction was analyzed by C NMR. C-isotopomer signals in the fatty acid ω - 1 and ω - 2 signals representing consecutive or non-consecutive enrichment of the fatty acid chain by [1,2- C ]acetyl-CoA were quantified and applied to a probabilistic model of acetyl-CoA precursor and fatty acid enrichment. Glucose contributed 72 ± 2% of lipogenic acetyl-CoA while DNL from all sources accounted for 16 ± 2% of lipid turnover. With LPS, there was a significant decrease in glucose contribution (59 ± 4%, p < 0.05) while DNL was unchanged (11 ± 3%). A simple C NMR analysis of the crude lipid fractions of BV-2 cells administered with [U- C]glucose informs DNL activity and the contribution of glucose to the acetyl-CoA precursors. While DNL was preserved in the presence of LPS, there was redirection of lipogenic acetyl-CoA sources from glucose to other substrates. Thus, in the present article, we describe a novel and simple C NMR analysis approach to disclose the overall lipogenic activity and substrate contribution to DNL, suitable for evaluating DNL rates in cell cultures.