Mammalian Lipin Phosphatidic Acid Phosphatases in Lipid Synthesis and Beyond: Metabolic and Inflammatory Disorders
Overview
Authors
Affiliations
The regulation of cellular lipid storage and membrane lipid composition plays a critical role in metabolic homeostasis, and dysregulation may contribute to disorders such as obesity, fatty liver, type 2 diabetes, and cardiovascular disease. The mammalian lipin proteins (lipin 1, lipin 2, and lipin 3) are phosphatidic acid phosphatase (PAP) enzymes that modulate levels of cellular triacylglycerols and phospholipids, and also regulate lipid intermediates in cellular signaling pathways. Lipin proteins also have the ability to coactivate/corepress transcription. In humans and mice, lipin gene mutations cause severe metabolic phenotypes including rhabdomyolysis (lipin 1), autoinflammatory disease (lipin 2), and impaired intestinal lipoprotein assembly (lipin 2/lipin 3). Characterization of these diseases has revealed roles for lipin PAP activity in fundamental cellular processes such as autophagy, inflammasome activation, and lipoprotein assembly. Lipin protein activity is regulated at pre- and posttranscriptional levels, which suggests a need for their ordered response to specific physiological stimuli. Challenges for the future include better elucidation of the unique biochemical and physiological properties of individual lipin family members and determination of lipin protein structure-function relationships. Further research may propel exploration of lipin proteins as viable therapeutic targets in metabolic or inflammatory disorders.
Insights into phosphatidic acid phosphatase and its potential role as a therapeutic target.
Carman G, Stukey G, Jog R, Han G Adv Biol Regul. 2025; 95:101074.
PMID: 39788800 PMC: 11832324. DOI: 10.1016/j.jbior.2025.101074.
Stukey G, Breuer M, Burchat N, Jog R, Schultz K, Han G J Lipid Res. 2024; 66(1):100711.
PMID: 39577771 PMC: 11721541. DOI: 10.1016/j.jlr.2024.100711.
The Role of Cardiolipin in Brain Bioenergetics, Neuroinflammation, and Neurodegeneration.
Bradshaw P, Aldridge J, Jamerson L, McNeal C, Pearson A, Frasier C Mol Neurobiol. 2024; .
PMID: 39557801 DOI: 10.1007/s12035-024-04630-6.
Structural basis of respiratory complex adaptation to cold temperatures.
Shin Y, Latorre-Muro P, Djurabekova A, Zdorevskyi O, Bennett C, Burger N Cell. 2024; 187(23):6584-6598.e17.
PMID: 39395414 PMC: 11601890. DOI: 10.1016/j.cell.2024.09.029.
CDS2 expression regulates de novo phosphatidic acid synthesis.
Collins D, Janardan V, Barneda D, Anderson K, Niewczas I, Taylor D Biochem J. 2024; 481(20):1449-1473.
PMID: 39312194 PMC: 11555650. DOI: 10.1042/BCJ20240456.