P4-ATPases translocate aminophospholipids, such as phosphatidylserine (PS), to the cytosolic leaflet of membranes. PS is highly enriched in recycling endosomes (REs) and is essential for endosomal membrane traffic. Here, we show that PS flipping by an RE-localized P4-ATPase is required for the recruitment of the membrane fission protein EHD1. Depletion of ATP8A1 impaired the asymmetric transbilayer distribution of PS in REs, dissociated EHD1 from REs, and generated aberrant endosomal tubules that appear resistant to fission. EHD1 did not show membrane localization in cells defective in PS synthesis. ATP8A2, a tissue-specific ATP8A1 paralogue, is associated with a neurodegenerative disease (CAMRQ). ATP8A2, but not the disease-causative ATP8A2 mutant, rescued the endosomal defects in ATP8A1-depleted cells. Primary neurons from Atp8a2−/− mice showed a reduced level of transferrin receptors at the cell surface compared to Atp8a2+/+ mice. These findings demonstrate the role of P4-ATPase in membrane fission and give insight into the molecular basis of CAMRQ.
Dynamic behaviors of liposomes caused by interactions between liposomal membranes and surfactant were studied by direct realtime observation by using high-intensity dark-field microscopy. Solubilization of liposomes by surfactants is thought to be a catastrophic event akin to the explosion of soap bubbles in the air; however, the actual process has not been clarified. We studied this process experimentally and found that liposomes exposed to various surfactants exhibited unusual behavior, namely continuous shrinkage accompanied by intermittent quakes, release of encapsulated liposomes, opening up, and inside-out topological inversion. L iposomes (which are closed membrane vesicles) have been well studied as simplified models of biological membranes (1-5) and are now used in a number of applications (5, 6), for example, as carriers of drug or DNA delivery or as artificial membranes for reconstructing membranous enzyme activities (7-9). Recently, many important phenomena affecting lipid bilayers, including their detergent solubilization, have been explored by using liposomes; such studies promote a better understanding of the biophysical properties of bilayer membranes and moreover will improve the handling of membrane proteins when they are isolated from or reconstructed into lipid bilayers (10-13). However, studies of intermediate stages in the detergent solubilization of liposomes are only now in progress (14-17), and the interaction mechanism between membranes and surfactants has remained unclear. Therefore, real-time approaches by using optical microscopy to study the dynamic behavior of liposomes are very important.High-intensity dark-field microscopy has enabled us to obtain real-time high-contrast images of giant unilamellar liposomes in aqueous solutions (18)(19)(20)(21)(22). In this study, we used such techniques to characterize the interactions between liposomal membranes and surfactants. Eight kinds of liposomes and various types of surfactants ( Fig. 1) were mixed in all possible combinations in a mixing chamber to generate a concentration gradient of each surfactant for microscope specimens, and morphological changes of liposomes exposed to those surfactants were monitored (18, 23). In the absence of surfactant, liposomal membranes were spherical, and thermal fluctuations of their spherical shape were largely suppressed by the surface tension of their membranes. Hereafter, this morphological state of liposomes will be called tense. In this study, we found several unusual behaviors of liposomes (which are published as supplemental data on the PNAS web site, www.pnas.org). Materials and MethodsPreparation and Observation of Liposomes. To prepare giant unilamellar liposome, liposome (total 1 mM lipid concentration) was made of phosphatidylcholine (PC) or of PC and one of seven other lipids (1:1, mol͞mol) in Hepes buffer (10 mM HepesNaOH, pH 7.0), as described previously (18,21,22). Lipids were dissolved in a chloroform͞methanol solution, 98:2 (vol͞vol), and mixed. The organic solvent was evaporated unde...
Substrate supported planar lipid bilayers (SPBs) are versatile models of the biological membrane in biophysical studies and biomedical applications. We previously developed a methodology for generating SPBs composed of polymeric and fluid phospholipid bilayers by using a photopolymerizable diacetylene phospholipid (DiynePC). Polymeric bilayers could be generated with micropatterns by conventional photolithography, and the degree of polymerization could be controlled by modulating UV irradiation doses. After removing nonreacted monomers, fluid lipid membranes could be integrated with polymeric bilayers. Herein, we report on a quantitative study of the morphology of polymeric bilayer domains and their obstruction toward lateral diffusion of membrane-associated molecules. Atomic force microscopy (AFM) observations revealed that polymerized DiynePC bilayers were formed as nanometer-sized domains. The ratio of polymeric and fluid bilayers could be modulated quantitatively by changing the UV irradiation dose for photopolymerization. Lateral diffusion coefficients of lipid molecules in fluid bilayers were measured by fluorescence recovery after photobleaching (FRAP) and correlated with the amount of polymeric bilayer domains on the substrate. Controlled domain structures, lipid compositions, and lateral mobility in the model membranes should allow us to fabricate model membranes that mimic complex features of biological membranes with well-defined structures and physicochemical properties.
Sphingomyelin (SM) is a major sphingolipid in mammalian cells and is reported to form specific lipid domains together with cholesterol. However, methods to examine the membrane distribution of SM are limited. We demonstrated in model membranes that fluorescent protein conjugates of 2 specific SM-binding toxins, lysenin (Lys) and equinatoxin II (EqtII), recognize different membrane distributions of SM; Lys exclusively binds clustered SM, whereas EqtII preferentially binds dispersed SM. Freeze-fracture immunoelectron microscopy showed that clustered but not dispersed SM formed lipid domains on the cell surface. Glycolipids and the membrane concentration of SM affect the SM distribution pattern on the plasma membrane. Using derivatives of Lys and EqtII as SM distribution-sensitive probes, we revealed the exclusive accumulation of SM clusters in the midbody at the time of cytokinesis. Interestingly, apical membranes of differentiated epithelial cells exhibited dispersed SM distribution, whereas SM was clustered in basolateral membranes. Clustered but not dispersed SM was absent from the cell surface of acid sphingomyelinasedeficient Niemann-Pick type A cells. These data suggest that both the SM content and membrane distribution are crucial for pathophysiological events bringing therapeutic perspective in the role of SM membrane distribution.-Makino, A., Abe, M., Murate, M., Inaba, T.,
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