Journal Article

Lipocalin 2 regulates mitochondrial phospholipidome remodeling, dynamics, and function in brown adipose tissue in male mice

Qiu, Xiaoxue, Qin, Chao, Bernlohr, David A., Yong, Peter, Guo, Hong, Senders, Mark, Han, Xianlin, Su, Hongming, Lin, Te-Yueh, Celio, Gail, Chen, Xiaoli

2023

Overview

Mitochondrial function is vital for energy metabolism in thermogenic adipocytes. Impaired mitochondrial bioenergetics in brown adipocytes are linked to disrupted thermogenesis and energy balance in obesity and aging. Phospholipid cardiolipin (CL) and phosphatidic acid (PA) jointly regulate mitochondrial membrane architecture and dynamics, with mitochondria-associated endoplasmic reticulum membranes (MAMs) serving as the platform for phospholipid biosynthesis and metabolism. However, little is known about the regulators of MAM phospholipid metabolism and their connection to mitochondrial function. We discover that LCN2 is a PA binding protein recruited to the MAM during inflammation and metabolic stimulation. Lcn2 deficiency disrupts mitochondrial fusion-fission balance and alters the acyl-chain composition of mitochondrial phospholipids in brown adipose tissue (BAT) of male mice. Lcn2 KO male mice exhibit an increase in the levels of CLs containing long-chain polyunsaturated fatty acids (LC-PUFA), a decrease in CLs containing monounsaturated fatty acids, resulting in mitochondrial dysfunction. This dysfunction triggers compensatory activation of peroxisomal function and the biosynthesis of LC-PUFA-containing plasmalogens in BAT. Additionally, Lcn2 deficiency alters PA production, correlating with changes in PA-regulated phospholipid-metabolizing enzymes and the mTOR signaling pathway. In conclusion, LCN2 plays a critical role in the acyl-chain remodeling of phospholipids and mitochondrial bioenergetics by regulating PA production and its function in activating signaling pathways. Mitochondrial function is essential for energy metabolism in brown adipocytes. Here, the authors show that LCN2 plays a critical role as a phosphatidic acid binding protein in phospholipid acyl chain remodeling and mitochondrial bioenergetics, influencing signaling pathway activation.

• Publisher: Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
• Subject: 13 / 13/51 / 14 / 14/19 / 14/28 / 38 / 38/77 / 49 / 631/443/319/2723 / 631/443/319/333 / 631/443/319/333/1465 / 64/60 / Adipocytes / Adipocytes, Brown - metabolism / Adipose tissue / Adipose tissue (brown) / Adipose Tissue, Brown - metabolism / Animals / Bioenergetics / Biosynthesis / Body fat / Cardiolipin / Endoplasmic reticulum / Energy balance / Energy metabolism / Fatty acids / Humanities and Social Sciences / Lipid metabolism / Lipocalin / Lipocalin-2 - metabolism / Male / Males / Membranes / Metabolism / Mice / Mice, Inbred C57BL / Mice, Knockout / Mitochondria / Mitochondria - metabolism / multidisciplinary / Phosphatidic acid / Phospholipids / Plasmalogens - metabolism / Polyunsaturated fatty acids / Proteins / Science / Science (multidisciplinary) / Signal transduction / Thermogenesis / Thermogenesis - genetics / TOR protein