DHA Modifies the Size and Composition of Raftlike Domains: A Solid-State 2H NMR Study

Docosahexaenoic acid is an omega-3 polyunsaturated fatty acid that relieves the symptoms of a wide variety of chronic inflammatory disorders. The structural mechanism is not yet completely understood. Our focus here is on the plasma membrane as a site of action. We examined the molecular organization of [H-2(31)]-N-palmitoylsphingomyelin (PSM-d(31)) mixed with 1-palmitoyl-2-docosahexaenoylphosphatylcholine (PDPC) or 1-palmitoyl-2-oleoylphosphatidylcholine (POPC), as a mono-unsaturated control, and cholesterol (chol) (1:1:1 mol) in a model membrane by solid-state H-2 NMR. The spectra were analyzed in terms of segregation into ordered SM-rich/chol-rich (raftlike) and disordered PC-rich/chol-poor (nonraft) domains that are nanoscale in size. An increase in the size of domains is revealed when POPC was replaced by PDPC. Spectra that are single-component, attributed to fast exchange between domains (<45 nm), for PSM-d(31) mixed with POPC and chol become two-component, attributed to slow exchange between domains (r>30 nm), for PSM-d(31) mixed with PDPC and chol. The resolution of separate signals from PSM-d(31), and correspondingly from [3 alpha-H-2(1)] cholesterol (chol-d(1)) and 1-[H-2(31)] palmitoyl-2-doco-sahexaenoylphosphatidylcholine (PDPC-d(31)), in raftlike and nonraft domains enabled us to determine the composition of the domains in the PDPC-containing membrane. Most of the lipid (28% SM, 29% chol, and 23% PDPC with respect to total lipid at 30 degrees C) was found in the raftlike domain. Despite substantial infiltration of PDPC into raftlike domains, there appears to be minimal effect on the order of SM, implying the existence of internal structure that limits contact between SM and PDPC. Our results suggest a significant refinement to the model by which DHA regulates the architecture of ordered, sphingolipid-chol-enriched domains (rafts) in membranes.