A new concept of cellular uptake and intracellular trafficking of long‐chain fatty acids

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Abstract
Fatty acids are the main structural and energy sources of the human body. Within the organism, they are presented to cells as fatty acid: albumin complexes. Dissociation from albumin represents the first step of the cellular uptake process, involving membrane proteins with high affinity for fatty acids, e.g., fatty acid translocase (FAT/CD 36) or the membrane fatty acid‐binding protein (FABPpm). According to the thus created transmembrane concentration gradient, uncharged fatty acids can flip‐flop from the outer leaflet across the phospholipid bilayer. At the cytosolic surface of the plasma membrane, fatty acids can associate with the cytosolic FABP (FABPc) or with caveolin‐1. Caveolins are constituents of caveolae, which are proposed to serve as lipid delivery vehicles for subcellular organelles. It is not known whether protein (FABPc)‐ and lipid (caveolae)‐mediated intracellular trafficking of fatty acids operates in conjunction, or in parallel. Channeling fatty acids to the different metabolic pathways requires activation to acyl‐CoA. For this process, the family of fatty acid transport proteins (FATP 1‐5/6) might be relevant because they have been shown to possess acyl‐CoA synthetase activity. Their variable N‐terminal signaling sequences suggest that they might be targeted to specific organelles by anchoring in the phospholipid bilayer of the different subcellular membranes. At the highly conserved cytosolic AMP‐binding site of FATP, fatty acids are activated to acyl‐CoA for subsequent metabolic disposition by specific organelles. Overall, fatty acid uptake represents a continuous flow involving the following: dissociation from albumin by membrane proteins with high affinity for fatty acids; passive flip‐flop across the phospholipid bilayer; binding to FABPc and caveolin‐1 at the cytosolic plasma membrane; and intracellular trafficking via FABPc and/or caveolae to sites of metabolic disposition. The uptake process is terminated after activation to acyl‐CoA by the members of the FATP family targeted intracellularly to different organelles.

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