Neutral glycolipids of atherosclerotic plaques and unaffected human aorta tissue

The composition, structure and localization of neutral glycosphingolipids of human aorta taken from subjects who had died after myocardial infarction were studied. Individual glycosphingolipids were purified by high‐performance liquid chromatography and were characterized on the basis of their chrom...

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Published inEuropean journal of biochemistry Vol. 180; no. 1; pp. 167 - 171
Main Authors PROKAZOVA, Nina V., MUKHIN, Dmitry N., OREKHOV, Alexander N., GLADKAYA, Elena M., VASILEVSKAYA, Valentina V., MIKHAILENKO, Irina A., SADOVSKAYA, Valentina L., BUSHUEV, Valery N., BERGELSON, Lev D.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.03.1989
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Abstract The composition, structure and localization of neutral glycosphingolipids of human aorta taken from subjects who had died after myocardial infarction were studied. Individual glycosphingolipids were purified by high‐performance liquid chromatography and were characterized on the basis of their chromatographic mobility, carbohydrate composition, methylation analysis and by 1H‐NMR spectroscopy. The main aortic glycosphingolipids were identified as glucosylceramide, lactosylceramide, globotriaosylceramide and globotetraosylceramide. Significant differences in the neutral glycosphingolipid composition of intima and media were detected. The neutral glycosphingolipid profile of medial plaques resembled that of unaffected media; however, significant differences were detected between intimal plaques and unaffected intima. Whereas the latter contained trihexosylceramide and globoside as the only neutral glycolipids, the intimal plaque glycolipids consisted mainly of glucosylceramide and also contained appreciable amounts of lactosylceramide which were completely absent in the unaffected intima. In comparison to intimal plaques, unaffected intima is characterized by a much higher content of cerebrosides terminating by β‐galactosyl residues which are known to interact with growth factors and other external stimuli. It thus seems possible that the proliferative activity of smooth muscle cells in atherosclerotic diseases is to some extent associated with their neutral glycolipid profile.
AbstractList The composition, structure and localization of neutral glycosphingolipids of human aorta taken from subjects who had died after myocardial infarction were studied. Individual glycosphingolipids were purified by high-performance liquid chromatography and were characterized on the basis of their chromatographic mobility, carbohydrate composition, methylation analysis and by 1H-NMR spectroscopy. The main aortic glycosphingolipids were identified as glucosylceramide, lactosylceramide, globotriaosylceramide and globotetraosylceramide. Significant differences in the neutral glycosphingolipid composition of intima and media were detected. The neutral glycosphingolipid profile of medial plaques resembled that of unaffected media; however, significant differences were detected between intimal plaques and unaffected intima. Whereas the latter contained trihexosylceramide and globoside as the only neutral glycolipids, the intimal plaque glycolipids consisted mainly of glucosylceramide and also contained appreciable amounts of lactosylceramide which were completely absent in the unaffected intima. In comparison to intimal plaques, unaffected intima is characterized by a much higher content of cerebrosides terminating by beta-galactosyl residues which are known to interact with growth factors and other external stimuli. It thus seems possible that the proliferative activity of smooth muscle cells in atherosclerotic diseases is to some extent associated with their neutral glycolipid profile.
The composition, structure and localization of neutral glycosphingolipids of human aorta taken from subjects who had died after myocardial infarction were studied. Individual glycosphingolipids were purified by high‐performance liquid chromatography and were characterized on the basis of their chromatographic mobility, carbohydrate composition, methylation analysis and by 1 H‐NMR spectroscopy. The main aortic glycosphingolipids were identified as glucosylceramide, lactosylceramide, globotriaosylceramide and globotetraosylceramide. Significant differences in the neutral glycosphingolipid composition of intima and media were detected. The neutral glycosphingolipid profile of medial plaques resembled that of unaffected media; however, significant differences were detected between intimal plaques and unaffected intima. Whereas the latter contained trihexosylceramide and globoside as the only neutral glycolipids, the intimal plaque glycolipids consisted mainly of glucosylceramide and also contained appreciable amounts of lactosylceramide which were completely absent in the unaffected intima. In comparison to intimal plaques, unaffected intima is characterized by a much higher content of cerebrosides terminating by β‐galactosyl residues which are known to interact with growth factors and other external stimuli. It thus seems possible that the proliferative activity of smooth muscle cells in atherosclerotic diseases is to some extent associated with their neutral glycolipid profile.
The composition, structure and localization of neutral glycosphingolipids of human aorta taken from subjects who had died after myocardial infarction were studied. Individual glycosphingolipids were purified by high‐performance liquid chromatography and were characterized on the basis of their chromatographic mobility, carbohydrate composition, methylation analysis and by 1H‐NMR spectroscopy. The main aortic glycosphingolipids were identified as glucosylceramide, lactosylceramide, globotriaosylceramide and globotetraosylceramide. Significant differences in the neutral glycosphingolipid composition of intima and media were detected. The neutral glycosphingolipid profile of medial plaques resembled that of unaffected media; however, significant differences were detected between intimal plaques and unaffected intima. Whereas the latter contained trihexosylceramide and globoside as the only neutral glycolipids, the intimal plaque glycolipids consisted mainly of glucosylceramide and also contained appreciable amounts of lactosylceramide which were completely absent in the unaffected intima. In comparison to intimal plaques, unaffected intima is characterized by a much higher content of cerebrosides terminating by β‐galactosyl residues which are known to interact with growth factors and other external stimuli. It thus seems possible that the proliferative activity of smooth muscle cells in atherosclerotic diseases is to some extent associated with their neutral glycolipid profile.
The composition, structure and localization of neutral glycosphingolipids of human aorta taken from subjects who had died after myocardial infarction were studied. Individual glycosphingolipids were purified by high-performance liquid chromatography and were characterized on the basis of their chromatographic mobility, carbohydrate composition, methylation analysis and by super(1)H-NMR spectroscopy. The main aortic glycosphingolipids were identified as glucosylceramide, lactosylceramide, globotriaosylceramide and globotetraosylceramide.
The composition, structure and localization of neutral glycosphingolipids of human aorta taken from subjects who had died after myocardial infarction were studied. Individual glycosphingolipids were purified by high-performance liquid chromatography and were characterized on the basis of their chromatographic mobility, carbohydrate composition, methylation analysis and by 1H-NMR spectroscopy. The main aortic glycosphingolipids were identified as glucosylceramide, lactosylceramide, globotriaosylceramide and globotetraosylceramide. Significant differences in the neutral glycosphingolipid composition of intima and media were detected. The neutral glycosphingolipid profile of medial plaques resembled that of unaffected media; however, significant differences were detected between intimal plaques and unaffected intima. Whereas the latter contained trihexosylceramide and globoside as the only neutral glycolipids, the intimal plaque glycolipids consisted mainly of glucosylceramide and also contained appreciable amounts of lactosylceramide which were completely absent in the unaffected intima. In comparison to intimal plaques, unaffected intima is characterized by a much higher content of cerebrosides terminating by beta-galactosyl residues which are known to interact with growth factors and other external stimuli. It thus seems possible that the proliferative activity of smooth muscle cells in atherosclerotic diseases is to some extent associated with their neutral glycolipid profile.The composition, structure and localization of neutral glycosphingolipids of human aorta taken from subjects who had died after myocardial infarction were studied. Individual glycosphingolipids were purified by high-performance liquid chromatography and were characterized on the basis of their chromatographic mobility, carbohydrate composition, methylation analysis and by 1H-NMR spectroscopy. The main aortic glycosphingolipids were identified as glucosylceramide, lactosylceramide, globotriaosylceramide and globotetraosylceramide. Significant differences in the neutral glycosphingolipid composition of intima and media were detected. The neutral glycosphingolipid profile of medial plaques resembled that of unaffected media; however, significant differences were detected between intimal plaques and unaffected intima. Whereas the latter contained trihexosylceramide and globoside as the only neutral glycolipids, the intimal plaque glycolipids consisted mainly of glucosylceramide and also contained appreciable amounts of lactosylceramide which were completely absent in the unaffected intima. In comparison to intimal plaques, unaffected intima is characterized by a much higher content of cerebrosides terminating by beta-galactosyl residues which are known to interact with growth factors and other external stimuli. It thus seems possible that the proliferative activity of smooth muscle cells in atherosclerotic diseases is to some extent associated with their neutral glycolipid profile.
Author GLADKAYA, Elena M.
MUKHIN, Dmitry N.
VASILEVSKAYA, Valentina V.
BUSHUEV, Valery N.
OREKHOV, Alexander N.
BERGELSON, Lev D.
MIKHAILENKO, Irina A.
SADOVSKAYA, Valentina L.
PROKAZOVA, Nina V.
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Cites_doi 10.1007/BF01108615
10.1111/j.1432-1033.1977.tb11778.x
10.1146/annurev.bi.50.070181.003505
10.1007/BF02533559
10.1016/0009-3084(74)90055-3
10.1016/0167-4889(88)90004-3
10.1139/v81-111
10.1159/000145868
10.1515/bchm2.1973.354.1.21
10.1038/325574a0
10.1111/j.1432-1033.1987.tb13343.x
10.4049/jimmunol.133.2.835
10.1021/bi00565a030
10.1016/0003-9861(87)90600-X
10.1042/bj2150261
10.1016/S0021-9258(18)32304-4
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Keywords Human
Atherosclerosis
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Aortic disease
Glycolipid
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References 1983; 215
1983; 258
1987; 167
1974; 12
1987; 256
1980; 19
1979; 14
1987; 325
1973; 35
1986; 3
1984; 10
1984; 33
1984; 79
1984; 115
1981; 46
1964; 55
1984; 119
1981; 59
1977; 79
1980
1981; 50
1988; 968
1989
1977; 81
e_1_2_2_3_2
e_1_2_2_24_2
e_1_2_2_23_2
e_1_2_2_5_2
e_1_2_2_22_2
e_1_2_2_21_2
e_1_2_2_20_2
e_1_2_2_2_2
Dyatlovitskaya E. V. (e_1_2_2_11_2) 1981; 46
e_1_2_2_19_2
e_1_2_2_18_2
e_1_2_2_7_2
e_1_2_2_16_2
e_1_2_2_15_2
Dyatlovitskaya E. V. (e_1_2_2_8_2) 1980
e_1_2_2_14_2
e_1_2_2_25_2
Prokazova N. V. (e_1_2_2_12_2) 1984; 10
Kavamura N. (e_1_2_2_9_2) 1977; 81
Orekhov A. N. (e_1_2_2_6_2) 1984; 115
Hakomori S.‐I. (e_1_2_2_13_2) 1964; 55
Wissler R. W. (e_1_2_2_4_2) 1984; 79
Urdal D. L. (e_1_2_2_17_2) 1983; 258
Okada Y. (e_1_2_2_10_2) 1984; 33
References_xml – volume: 33
  start-page: 835
  year: 1984
  end-page: 842
  publication-title: J. Immunol.
– volume: 55
  start-page: 205
  year: 1964
  end-page: 208
  publication-title: J. Biochem. (Tokyo)
– volume: 14
  start-page: 9
  year: 1979
  end-page: 14
  publication-title: Lipids
– volume: 115
  start-page: 17
  year: 1984
  end-page: 24
  publication-title: Am. J. Pathol.
– volume: 258
  start-page: 6869
  year: 1983
  end-page: 6874
  publication-title: J. Biol. Chem.
– volume: 325
  start-page: 574
  year: 1987
  end-page: 575
  publication-title: Nature (Lond.)
– volume: 968
  start-page: 167
  year: 1988
  end-page: 171
  publication-title: Biochim. Biophys. Acta
– start-page: 244
  year: 1980
– volume: 59
  start-page: 412
  year: 1981
  end-page: 417
  publication-title: Can. J. Biochem.
– volume: 81
  start-page: 1217
  year: 1977
  end-page: 1225
  publication-title: J. Biochem. (Tokyo)
– year: 1989
– volume: 215
  start-page: 261
  year: 1983
  end-page: 272
  publication-title: Biochem. J.
– volume: 79
  start-page: 11
  year: 1977
  end-page: 12
  publication-title: Eur. J. Biochem.
– volume: 19
  start-page: 5652
  year: 1980
  end-page: 5658
  publication-title: Biochemistry
– volume: 12
  start-page: 271
  year: 1974
  end-page: 284
  publication-title: Chem. Phys. Lipids
– volume: 3
  start-page: 95
  year: 1986
  end-page: 108
  publication-title: Glycoconjugate J.
– volume: 256
  start-page: 435
  year: 1987
  end-page: 445
  publication-title: Arch. Biochem. Biophys.
– volume: 50
  start-page: 733
  year: 1981
  end-page: 764
  publication-title: Annu. Rev. Biochem.
– volume: 10
  start-page: 238
  year: 1984
  end-page: 243
  publication-title: Bioorg. Khim.
– volume: 46
  start-page: 2004
  year: 1981
  end-page: 2010
  publication-title: Biokhimia
– volume: 79
  start-page: 5
  year: 1984
  end-page: 20
  publication-title: NATO Adv. Study Inst. Ser. Ser. A, Life Sci.
– volume: 119
  start-page: 99
  year: 1984
  end-page: 105
  publication-title: Acta Anat.
– volume: 35
  start-page: 21
  year: 1973
  end-page: 31
  publication-title: Hoppe-Seyler's Z. Physiol. Chem. B.
– volume: 167
  start-page: 349
  year: 1987
  end-page: 352
  publication-title: Eur. J. Biochem.
– ident: e_1_2_2_2_2
  doi: 10.1007/BF01108615
– volume: 46
  start-page: 2004
  year: 1981
  ident: e_1_2_2_11_2
  publication-title: Biokhimia
– ident: e_1_2_2_25_2
  doi: 10.1111/j.1432-1033.1977.tb11778.x
– ident: e_1_2_2_3_2
  doi: 10.1146/annurev.bi.50.070181.003505
– volume: 79
  start-page: 5
  year: 1984
  ident: e_1_2_2_4_2
  publication-title: NATO Adv. Study Inst. Ser. Ser. A, Life Sci.
– ident: e_1_2_2_20_2
  doi: 10.1007/BF02533559
– ident: e_1_2_2_18_2
  doi: 10.1016/0009-3084(74)90055-3
– ident: e_1_2_2_24_2
  doi: 10.1016/0167-4889(88)90004-3
– volume: 81
  start-page: 1217
  year: 1977
  ident: e_1_2_2_9_2
  publication-title: J. Biochem. (Tokyo)
– ident: e_1_2_2_19_2
  doi: 10.1139/v81-111
– ident: e_1_2_2_7_2
  doi: 10.1159/000145868
– volume: 10
  start-page: 238
  year: 1984
  ident: e_1_2_2_12_2
  publication-title: Bioorg. Khim.
– ident: e_1_2_2_15_2
  doi: 10.1515/bchm2.1973.354.1.21
– start-page: 244
  volume-title: Lipid biochemical preparations
  year: 1980
  ident: e_1_2_2_8_2
– ident: e_1_2_2_21_2
  doi: 10.1038/325574a0
– ident: e_1_2_2_5_2
  doi: 10.1111/j.1432-1033.1987.tb13343.x
– volume: 33
  start-page: 835
  year: 1984
  ident: e_1_2_2_10_2
  publication-title: J. Immunol.
  doi: 10.4049/jimmunol.133.2.835
– volume: 115
  start-page: 17
  year: 1984
  ident: e_1_2_2_6_2
  publication-title: Am. J. Pathol.
– ident: e_1_2_2_16_2
  doi: 10.1021/bi00565a030
– ident: e_1_2_2_22_2
  doi: 10.1016/0003-9861(87)90600-X
– ident: e_1_2_2_14_2
  doi: 10.1042/bj2150261
– volume: 55
  start-page: 205
  year: 1964
  ident: e_1_2_2_13_2
  publication-title: J. Biochem. (Tokyo)
– volume: 258
  start-page: 6869
  year: 1983
  ident: e_1_2_2_17_2
  publication-title: J. Biol. Chem.
  doi: 10.1016/S0021-9258(18)32304-4
– ident: e_1_2_2_23_2
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Snippet The composition, structure and localization of neutral glycosphingolipids of human aorta taken from subjects who had died after myocardial infarction were...
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crossref
wiley
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StartPage 167
SubjectTerms Adult
Antigens, CD
aorta
Aorta, Thoracic - metabolism
Arteriosclerosis - complications
Arteriosclerosis - metabolism
Atherosclerosis (general aspects, experimental research)
Biological and medical sciences
Blood and lymphatic vessels
Cardiology. Vascular system
Chromatography, High Pressure Liquid
Chromatography, Thin Layer
Fatty Acids - analysis
Female
Globosides - analysis
glycolipids
Glycolipids - analysis
Glycosphingolipids - analysis
Humans
Lactosylceramides
Magnetic Resonance Spectroscopy
Male
Mass Spectrometry
Medical sciences
Middle Aged
Muscle, Smooth, Vascular - metabolism
Myocardial Infarction - complications
Myocardial Infarction - metabolism
Title Neutral glycolipids of atherosclerotic plaques and unaffected human aorta tissue
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1432-1033.1989.tb14628.x
https://www.ncbi.nlm.nih.gov/pubmed/2707259
https://www.proquest.com/docview/15280586
https://www.proquest.com/docview/78935807
Volume 180
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