Phosphoproteomic Analysis of Subcutaneous and Omental Adipose Tissue Reveals Increased Lipid Turnover in Dairy Cows Supplemented with Conjugated Linoleic Acid

• Published in: International journal of molecular sciences Vol. 22; no. 6; p. 3227
• Main Authors: Daddam, Jayasimha Rayalu, Hammon, Harald M, Tröscher, Arnulf, Vogel, Laura, Gnott, Martina, Kra, Gitit, Levin, Yishai, Sauerwein, Helga, Zachut, Maya
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI 22.03.2021; MDPI AG
• Subjects: adipose tissue; Adipose Tissue - metabolism; Animals; Biomarkers; Cattle; Computational Biology - methods; conjugated linoleic acid; Dietary Supplements; endocannabinoid system; fatty acid synthase; Gene Ontology; Linoleic Acids, Conjugated - administration & dosage; Linoleic Acids, Conjugated - metabolism; Lipid Metabolism; Lipogenesis; Milk; Omentum; Phosphoproteins - metabolism; phosphoproteomics; Proteome; Proteomics - methods; Subcutaneous Fat - metabolism; phosphoproteomics; conjugated linoleic acid; dairy cow; fatty acid synthase; lipid metabolism; adipose tissue; endocannabinoid system
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms22063227

Phosphoproteomics is a cutting-edge technique that can be utilized to explore adipose tissue (AT) metabolism by quantifying the repertoire of phospho-peptides (PP) in AT. Dairy cows were supplemented with conjugated linoleic acid (CLA, = 5) or a control diet (CON, = 5) from 63 d prepartum to 63 d postpartum; cows were slaughtered at 63 d postpartum and AT was collected. We performed a quantitative phosphoproteomics analysis of subcutaneous (SC) and omental (OM) AT using nanoUPLC-MS/MS and examined the effects of CLA supplementation on the change in the phosphoproteome. A total of 5919 PP were detected in AT, and the abundance of 854 (14.4%) were differential between CON and CLA AT ( ≤ 0.05 and fold change ± 1.5). The abundance of 470 PP (7.9%) differed between OM and SC AT, and the interaction treatment vs. AT depot was significant for 205 PP (3.5% of total PP). The integrated phosphoproteome demonstrated the up- and downregulation of PP from proteins related to lipolysis and lipogenesis, and phosphorylation events in multiple pathways, including the regulation of lipolysis in adipocytes, mTOR signaling, insulin signaling, AMPK signaling, and glycolysis. The differential regulation of phosphosite on a serine residue (S777) of fatty acid synthase (FASN) in AT of CLA-supplemented cows was related to lipogenesis and with more phosphorylation sites compared to acetyl-coenzyme A synthetase (ACSS2). Increased protein phosphorylation was seen in acetyl-CoA carboxylase 1 (ACACA;8 PP), FASN (9 PP), hormone sensitive lipase (LIPE;6 PP), perilipin (PLIN;3 PP), and diacylglycerol lipase alpha (DAGLA;1 PP) in CLA vs. CON AT. The relative gene expression in the SC and OM AT revealed an increase in and in CLA compared to CON AT. In addition, the expression of , which is a lipid metabolism enzyme related to the endocannabinoid system, was 1.6-fold higher in CLA vs. CON AT, and the expression of the cannabinoid receptor was reduced in CLA vs. CON AT. Immunoblots of SC and OM AT showed an increased abundance of FASN and a lower abundance of CB1 in CLA vs. CON. This study presents a complete map of the SC and the OM AT phosphoproteome in dairy cows following CLA supplementation and discloses many unknown phosphorylation sites, suggestive of increased lipid turnover in AT, for further functional investigation.