ABSTRACT
The plasmalogens are a class of glycerophospholipids which contain a vinyl-ether and an ester bond at the sn-1 and sn-2 positions, respectively, in the glycerol backbone. They constitute 10 mol% of the total mass of phospholipids in humans, mainly as membrane structure components. Plasmalogens are important for the organization and stability of lipid raft microdomains and cholesterol-rich membrane regions involved in cellular signaling. In addition to their structural roles, a subset of ether lipids are thought to function as endogenous antioxidants and emerging studies suggest that they are involved in cell differentiation and signaling pathways. Although the clinical significance of plasmalogens is linked to peroxisomal disorders, the pathophysiological roles and their possible metabolic pathways are not fully understood since they present unique structural attributes for the different tissue types. Studies suggest that changes in plasmalogen metabolism may contribute to the development of various types of cancer. Here, we review the molecular characteristics of plasmalogens in order to significantly increase our understanding of the plasmalogen molecule and its involvement in gastrointestinal cancers as well as other types of cancers.
Subject(s)
Antineoplastic Agents/pharmacology , Gastrointestinal Neoplasms/etiology , Plasmalogens/metabolism , Plasmalogens/pharmacology , Antineoplastic Agents/chemistry , Biomarkers, Tumor/metabolism , Gastrointestinal Neoplasms/drug therapy , Humans , Lipid Metabolism , Phospholipid Ethers/pharmacologyABSTRACT
Cyclopropane fatty acid synthase (CFAS) catalyzes the transfer of a methylene group from S-adenosyl methionine to an unsaturated fatty acid, generating a cyclopropane fatty acid (CFA). The gene encoding CFAS is present in many bacteria and several Leishmania spp. including Leishmania mexicana, Leishmania infantum and Leishmania braziliensis. In this study, we characterised the CFAS-null and -overexpression mutants in L. mexicana, the causative agent for cutaneous leishmaniasis in Mexico and central America. Our data indicate that L. mexicana CFAS modifies the fatty acid chain of plasmenylethanolamine (PME), the dominant class of ethanolamine glycerophospholipids in Leishmania, generating CFA-PME. While the endogenous level of CFA-PME is extremely low in wild type L. mexicana, overexpression of CFAS results in a significant increase. CFAS-null mutants (cfas-) exhibit altered cell shape, increased sensitivity to acidic pH, and aberrant growth in serum-free media. In addition, the CFAS protein is preferentially expressed during the proliferative stage of L. mexicana and is required for the cell membrane targeting of lipophosphoglycan. Finally, the maturation and localization of CFAS protein are dependent upon the downstream sequence of the CFAS coding region. Without the downstream sequence, the mis-localised CFAS protein cannot fully rescue the defects of cfas-. Our data suggest that CFA modification of phospholipids can significantly affect the parasite's response to certain adverse conditions. These findings are distinct from the roles of CFAS in L. infantum, highlighting the functional divergence in lipid modification among Leishmania spp.
Subject(s)
Fatty Acids/biosynthesis , Leishmania mexicana/metabolism , Methyltransferases/metabolism , Animals , Blotting, Southern , Blotting, Western , Cyclopropanes , Hydrogen-Ion Concentration , Leishmania mexicana/cytology , Leishmania mexicana/drug effects , Leishmania mexicana/genetics , Leishmaniasis, Cutaneous/parasitology , Lipids/analysis , Macrophages/parasitology , Methyltransferases/chemistry , Methyltransferases/genetics , Mice , Mice, Inbred BALB C , Microscopy, Fluorescence , Plasmalogens/chemistry , Plasmalogens/metabolism , Spectrometry, Mass, Electrospray Ionization , Spectroscopy, Fourier Transform InfraredABSTRACT
Dietary rumen-protected polyunsaturated fatty acids (PUFAs) rich in linoleic acid (LA) may affect embryo yield, and LA can modulate the molecular mechanisms of lipid uptake in bovine blastocysts produced in vitro. In embryos, membrane lipids, such as phosphatidylcholines (PCs) and sphingomyelins (SMs), affect cryopreservation success. The aim of the present study was to evaluate embryonic developmental rates after the IVF of oocytes retrieved from Nellore heifers fed for approximately 90 days with rumen-protected PUFAs rich in LA. In addition, we evaluated embryo cryotolerance and the membrane structure lipid composition using matrix-assisted laser desorption ionisation mass spectrometry of fresh and vitrified embryos. Embryo development to the blastocyst stage (mean 43.2%) and embryo survival after vitrification and warming (mean 79.3%) were unaffected by diet. The relative abundance of one lipid species (PC ether (PCe; 38:2, which means that this lipid has 38 carbon atoms and 2 double bonds in the fatty acyl residues) was increased after PUFAs supplementation. However, 10 ions were affected by cryopreservation; ions consistent with PC 32:0, PC 34:1, SM 24:1, PC 40:6 or PC 42:9, PC plasmalogen (PCp) 44:10 or PC 42:7, triacylglycerol (TAG) 54:9 and a not assigned ion (m/z 833.2) were lower in blastocysts that survived to the cryopreservation process compared with fresh blastocysts, whereas the abundance of the ions PC 36:3 or PC 34:0, PCe 38:2 or PC 36:6 and PC 36:5 or PCe 38:1 were increased after cryopreservation. Thus, the results demonstrate that the mass spectrometry profiles of PC, SM and TAG species differ significantly in bovine blastocysts upon cryopreservation. Because the lipid ion abundances of fresh and vitrified-warmed embryos were distinct, they can be used as potential markers of post-cryopreservation embryonic survival.
Subject(s)
Cryopreservation/veterinary , Dietary Fats, Unsaturated/administration & dosage , Ectogenesis , Embryo, Mammalian/metabolism , Maternal Nutritional Physiological Phenomena , Membrane Lipids/metabolism , Oocysts/metabolism , Animals , Animals, Inbred Strains , Blastocyst , Brazil , Cattle , Cross-Over Studies , Embryo, Mammalian/cytology , Female , Fertilization in Vitro/veterinary , In Vitro Oocyte Maturation Techniques/veterinary , Linoleic Acid/administration & dosage , Linoleic Acid/metabolism , Male , Membrane Lipids/chemistry , Oocysts/cytology , Oocysts/isolation & purification , Oocyte Retrieval/veterinary , Plasmalogens/chemistry , Plasmalogens/metabolism , Semen Preservation/veterinary , VitrificationABSTRACT
Antigen tumor markers employed in monitoring therapeutical approaches are limited by their specificity (Sp) and sensitivity (Se). The aim of this study was to investigate the suitability of a lipid tumor marker derived from ether-linked phospholipids and to compare it with others usually assayed in clinical practice. Complex lipids from normal and pathological breast, lung, and prostate tissue were isolated and analyzed by TLC and c-GLC methods. Results were compared as pooled samples, or by means of the averaged percent changes with respect to the composition observed in the normal tissue of the same patient. Sp, Se, negative-predictive (NPV) and positive- predictive values (PPV) were established for conventional markers and for the proposed lipid-derived marker. Results demonstrated that the content of monoenoic fatty acyl chains was significantly increased in total lipids, phosphatidylethanolamine, and especially in ethanolamine-containing ether lipids of neoplastic tissues with respect to their corresponding normal ones. Major changes were observed in the plasmalogen sub-fraction where the ratio monoenoic/saturated fatty acids can distinguish with high Se normal tissues from either benign or neoplastic tissues from breast, lung, or prostate lesions. Analyses of fatty acyl chains from ethanolamine-containing plasmalogens provided a reliable tumor marker that correlated with high Se and linearity with metastases spreading. This fact may be useful in prognosis of the most frequently observed human cancers.
Subject(s)
Biomarkers, Tumor/blood , Neoplasms/blood , Neoplasms/diagnosis , Plasmalogens/blood , Aged , Aged, 80 and over , Ethanolamine/analysis , Female , Humans , Lipids/blood , Male , Middle Aged , Neoplasm Metastasis , Plasmalogens/chemistry , Predictive Value of Tests , Prognosis , Regression Analysis , Sensitivity and SpecificityABSTRACT
A novel phospholipid has been purified from strain Dm 28c of Trypanosoma cruzi, and characterized by fast atom bombardment mass spectrometry and nuclear magnetic resonance spectroscopy as a plasmenylethanolamine with a hexadec-l-enyl group in the sn-1 position and an approximately equimolar mixture of octadecenoate and octadecadienoate esterified to the sn-2 hydroxyl. The purified plasmenylethanolamine reacted positively when probed with sera from patients with chronic Chagas' disease. Since plasmenylethanolamines of similar structure are abundant in mammalian cardiac and neuronal tissues, cross reactions between these epitopes may be a factor in the mechanism of autoimmune pathology in the chronic phase of Chagas' disease.
Subject(s)
Phospholipids/chemistry , Plasmalogens/analysis , Trypanosoma cruzi/chemistry , Animals , Antibodies, Protozoan/blood , Chagas Disease/blood , Chromatography, High Pressure Liquid , Chromatography, Thin Layer , Clone Cells , Fatty Acids, Unsaturated/analysis , Gas Chromatography-Mass Spectrometry , Humans , Nuclear Magnetic Resonance, Biomolecular , Phospholipids/immunology , Plasmalogens/immunology , Spectrometry, Mass, Fast Atom Bombardment , Stearic Acids/analysisABSTRACT
Os fatores de risco para tromboses såo reconhecidos há muitos anos, mas os estudos laboratoriais até recentemente eram pouco informativos. Na última década, verificou-se que parte dos casos de tromboembolismos venosos está associada a deficiências dos sistemas de anticoagulaçåo matural e de plasminogênio. O objetivo deste trabalho é avaliar a incidência destes déficits em pacientes com tromboembolismo, no nosso meio. Cinqüenta e dois pacientes sem anticoagulaçåo oral foram investigados com testes funcionais por coagulaçåo para proteína C (PC) e antitrombina III (ATIII) e teste de imunológicos (Laurell) para proteína S (PS) e (Mancinni) para plaminogênio. Na presenca de déficits de PC, realizaram-se dosagens amidolíticas confirmatórias. Identificaram-se oito (15,4 por cento) pacientes com alteraçöes: um com déficit de ATIII, cinco de PC isolada e dois com deficiência combinada de PC e PS. Nenhum caso de deficiência de plasminogênio foi encontrado. Os testes funcionais hepáticos destes oito pacientes foram normais. Estudo familiar de triagem foi possível em três casos, comdetecçåo de novos portadores em dois. Houve atraso médio de 27 meses entre o episódio comprovado de tromboembolismo e o diagnóstico hematológico. Os pacientes deficientes parecem estar mais predispostos à recorrência tromboembólica do que os nåo-deficientes. A freqüência de alteraçöes de PC é superior à esperada, tal ocorrência podendo ser devida ao tipo de triagem (estudo monocêntrico) ou à prevalência maior desta alteraçåo no nosso meio
Subject(s)
Humans , Male , Female , Adult , Middle Aged , Blood Coagulation , Thromboembolism , Antithrombin III , Plasmalogens/blood , Protein C , ProteinsABSTRACT
Dietary deficiency of essential fatty acids of the n-3 and n-6 series is known to promote a compensatory increase in polyenoic fatty acids of the n-9 series in the lipids of mammalian tissues. In the present study long-chain n-9 polyenes were found to be normal components of the epididymis and especially of sperm isolated from that tissue, in healthy, well-fed, fertile rats maintained on essential fatty acid-sufficient diets. The n-9 polyenes occurred in large concentrations in the choline glycerophospholipids (CGP), the major phospholipid class of spermatozoa in epididymal cauda, and were highly concentrated in plasmenylcholine, the major subclass of CGP. The uncommon polyene 22:4n-9 was found in the highest proportion, followed in order of relative abundance by 22:3n-9, 20:3n-9 and 24:4n-9. These polyenes were probably derived from oleate (18:1n-9) in much the same way as long-chain polyenes of the n-6 and n-3 series are derived from linoleate (18:2n-6) and linolenate (18:3n-3), respectively.
Subject(s)
Epididymis/chemistry , Fatty Acids, Unsaturated/analysis , Spermatozoa/chemistry , Animals , Diet , Fertility/physiology , Male , Models, Biological , Phosphatidylcholines/analysis , Phosphatidylethanolamines/analysis , Plasmalogens/analysis , Rats , Rats, Inbred Strains , Rats, Wistar , Tissue DistributionABSTRACT
In their transit from the caput to the cauda segments of the epididymis, rat spermatozoa undergo significant modifications in lipid content and composition. The amount of lipid phosphorus per cell decreases, and most lipid classes show specific changes in their constituent fatty acids. A depletion of phosphatidylcholine and phosphatidylethanolamine, concomitant with a virtually unchanged amount of the corresponding plasmalogens, are the major alterations, plasmenylcholine thereby becoming the major phospholipid. Diphosphatidylglycerol, sphingomyelin and the phosphoinositides decrease to a lesser extent or do not change at all, also resulting in relative increases with sperm maturation. Concerning the fatty acids, the proportions of oleate (C18:1, n-9) and linoleate (C18:2, n-6) in most lipids decrease on movement of sperm from caput to cauda, augmenting in turn the proportions of longer-chain (C20 to C24) and more unsaturated fatty acids. Docosapentaenoate (C22:5, n-6) is a major acyl chain present in all lipids at both stages, but uncommon long-chain polyenoic fatty acids of the n-9 series are also present, being almost exclusively found in the choline glycerophospholipids. These fatty acids are found to undergo the most significant changes during sperm maturation. They are minor components of plasmenylcholine in immature spermatozoa, but increase severalfold on maturation, representing more than half of the acyl chains of this major lipid in cells from the cauda. The high concentration of n-9 polyenes in mature sperm plasmenylcholine raises intriguing questions on the possible role epididymal cells may play in providing spermatozoa with such an unusual phospholipid. These plasmenylcholines could contribute to the characteristic lipid domain organization of the mature spermatozoa plasma membrane.
Subject(s)
Epididymis/metabolism , Fatty Acids, Unsaturated/metabolism , Lipid Metabolism , Plasmalogens/metabolism , Spermatozoa/growth & development , Animals , Epididymis/growth & development , Epididymis/physiology , In Vitro Techniques , Male , Phosphatidylcholines/metabolism , Phospholipids/metabolism , Rats , Rats, Inbred Strains , Sexual Maturation/physiology , Spermatozoa/metabolismABSTRACT
Biochemical studies with emphasis on peroxisomal functions were conducted in six patients with well-documented rhizomelic chondrodysplasia punctata (RCDP) and compared with findings in patients with Zellweger syndrome and neonatal adrenoleukodystrophy (ALD). Patients with RCDP had three characteristic biochemical abnormalities: (1) profound defect in plasmalogen (ether lipid) synthesis, which is significantly greater than the analogous defect in Zellweger syndrome or neonatal ALD; (2) reduction of phytanic acid oxidation activity to 1% to 5% of control, similar to that observed in Refsum disease, Zellweger syndrome, and neonatal ALD; (3) presence of the unprocessed form of peroxisomal 3-oxoacyl-coenzyme A thiolase in the postmortem liver of two patients. Other peroxisomal functions were normal, including levels of very long chain fatty acids, pipecolic acid, and bile acid intermediates, and immunoblot studies of peroxisomal acyl-CoA oxidase and bifunctional enzyme in postmortem liver. Unlike what is observed in Zellweger syndrome and neonatal ALD, catalase activity in cultured skin fibroblasts was sedimentable, indicating that peroxisome structure is not grossly deficient in RCDP. The biochemical abnormalities in RCDP were consistent and set it apart from all the other known peroxisomal disorders.
Subject(s)
Chondrodysplasia Punctata/metabolism , Microbodies/metabolism , Acetyl-CoA C-Acyltransferase/metabolism , Adrenoleukodystrophy/metabolism , Female , Fibroblasts/metabolism , Humans , Infant , Infant, Newborn , Liver/metabolism , Male , Phytanic Acid/metabolism , Plasmalogens/biosynthesis , Refsum Disease/metabolismABSTRACT
The level and proportion of lipids and their fatty acid composition were analyzed in highly purified transverse tubule membranes of amphibian skeletal muscle. Tubule membranes show (a) a higher content of lipids, (b) a higher phospholipid/cholesterol ratio and (c) a different phospholipid composition from other subcellular fractions, such as the light and heavy membranes from sarcoplasmic reticulum, which are similar in lipid profile. Transverse tubule membranes are characterized by a high percentage of phosphatidylserine and sphingomyelin and a low proportion of phosphatidylcholine compared with the other membranes. All three show a high proportion of ethanolamine plasmalogens (50% of the total ethanolamine glycerophospholipid). Transverse tubule membrane lipids contain a high proportion of 20- and 22-carbon polyunsaturated fatty acids, predominantly 20:4, 20:5, 22:5 and 22:6. Arachidonate predominates in phosphatidylinositol, eicosapentaenoate and docosahexaenoate in ethanolamine and serine glycerophospholipids.
Subject(s)
Intracellular Membranes/analysis , Membrane Lipids/analysis , Muscles/analysis , Animals , Anura , Arachidonic Acid , Arachidonic Acids/analysis , Cholesterol/analysis , Fatty Acids/analysis , Fatty Acids, Unsaturated/analysis , Muscles/ultrastructure , Phosphatidylserines/analysis , Phospholipids/analysis , Plasmalogens/analysis , Sphingomyelins/analysisSubject(s)
Bile Acids and Salts/blood , Hepatorenal Syndrome/complications , Kidney Diseases/complications , Metabolism, Inborn Errors/complications , Microbodies/metabolism , Plasmalogens/blood , Skull/abnormalities , Chromosome Aberrations/blood , Chromosome Aberrations/diagnosis , Chromosome Disorders , Hepatorenal Syndrome/diagnosis , Hepatorenal Syndrome/genetics , Humans , Infant, Newborn , Metabolism, Inborn Errors/diagnosis , Metabolism, Inborn Errors/genetics , Prenatal Diagnosis , SyndromeABSTRACT
A boy with psychomotor retardation and Leber congenital amaurosis, sensory hearing loss, and hepatomegaly is reported. Accumulation of bile acid precursors and very long chain fatty acids together with impaired biosynthesis of plasmalogens in cultured fibroblasts (similar to those in the cerebrohepatorenal syndrome of Zellweger) were detected, but the clinical picture was distinctly different. Defective oxidation of phytanic acid was measured in fibroblasts. The virtual lack of peroxisomes in a liver biopsy specimen lends further support to the contention that at least some patients with Leber congenital amaurosis may have one of the recently defined "peroxisomal disorders." The biochemical findings indicate the possibility of prenatal diagnosis.