Lipid-modifying enzymes dynamically regulate membrane architecture, signaling compartmentalization, and inter-organ metabolic communication, thereby influencing systemic glucose homeostasis. Advances in lipidomics and structural enzymology reveal how enzymatic remodeling of phospholipids, sphingolipids, and acyl chains governs insulin receptor organization, PI3K-AKT signaling, and GLUT4 trafficking. Dysregulated lipid flux mediated by factors such as FABP4, ceramides, and diacylglycerols disrupts membrane microdomains, impairs β-cell function, and promotes hepatic gluconeogenesis and skeletal muscle insulin resistance. Conversely, omega-3 polyunsaturated fatty acids enhance membrane fluidity and anti-inflammatory signaling. Integrating lipid enzymology with metabolic physiology establishes a unified mechanistic framework linking membrane remodeling to insulin responsiveness and diabetes pathogenesis.
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Nila Ganamurali
Sarvesh Sabarathinam
Navodi Sandamini Jayathilaka
Saveetha University
University of Sri Jayewardenepura
Dr. M.G.R. Educational and Research Institute
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Ganamurali et al. (Wed,) studied this question.
www.synapsesocial.com/papers/69ada885bc08abd80d5bb81c — DOI: https://doi.org/10.1002/cph4.70125