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      역상HPLC컬럼을 이용한 생체 내 단당세라마이드 분석 = Determination of Monoglycoceramides in Biological Samples using Enzymatic Deacylation and Reverse-phase HPLC

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      https://www.riss.kr/link?id=A100412920

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Glycosphingolipids are structural components of mammalian cell membranes and are involved in essential cellular physiology such as cell-cell interaction, recognition, transmembrane signaling, proliferation and cell death. In this study, the simple quantitative method of monoglycoceramides-containing glucosylceramide and galactosylceramide was developed. The glycosylceramides extracted from culture cells and rat plasma were resolved by TLC, deacylated by SCDase and analyzed by HPLC-fluorescence detector at an excitation wavelength of 340 nm and an emission wavelength of 455 nm. Limit of detection was approximately 0.1 pmol and limit of quantification was about 1 pmol for both monoglycoceramide standards. The recoveries of standard glucosylceramides from intra- and inter-day assays were 113.8 and 88.8% and those of galactosylceramides were 110.7 and 123.9%, respectively. The monoglycoceramide contents of SW-620 cells and rat plasma were 141.5±5 pmol/1×106 cells and 3.9±0.3 μM, respectively. The present analytical method provides a reproducible quantification and total content of monoglycoceramide which may be as a potential biomarker for lipid imbalance-related human diseases.
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      Glycosphingolipids are structural components of mammalian cell membranes and are involved in essential cellular physiology such as cell-cell interaction, recognition, transmembrane signaling, proliferation and cell death. In this study, the simple qua...

      Glycosphingolipids are structural components of mammalian cell membranes and are involved in essential cellular physiology such as cell-cell interaction, recognition, transmembrane signaling, proliferation and cell death. In this study, the simple quantitative method of monoglycoceramides-containing glucosylceramide and galactosylceramide was developed. The glycosylceramides extracted from culture cells and rat plasma were resolved by TLC, deacylated by SCDase and analyzed by HPLC-fluorescence detector at an excitation wavelength of 340 nm and an emission wavelength of 455 nm. Limit of detection was approximately 0.1 pmol and limit of quantification was about 1 pmol for both monoglycoceramide standards. The recoveries of standard glucosylceramides from intra- and inter-day assays were 113.8 and 88.8% and those of galactosylceramides were 110.7 and 123.9%, respectively. The monoglycoceramide contents of SW-620 cells and rat plasma were 141.5±5 pmol/1×106 cells and 3.9±0.3 μM, respectively. The present analytical method provides a reproducible quantification and total content of monoglycoceramide which may be as a potential biomarker for lipid imbalance-related human diseases.

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      참고문헌 (Reference)

      1 Pewzner-Jung, Y, "When do Lasses (longevity assurance genes) become CerS (ceramide synthases)?: Insights into the regulation of ceramide synthesis" 281 : 25001-, 2006

      2 Tafesse, F. G, "The multigenic sphingomyelin synthase family" 281 : 29421-, 2006

      3 Hakomori, S, "The hapten structure of a developmentally regulated glycolipid antigen (SSEA-1) isolated from human erythrocytes and adenocarcinoma: a preliminary note" 100 : 1578-, 1981

      4 Chakrabandhu, K, "The extracellular glycosphingolipid-binding motif of Fas defines its internalization route, mode and outcome of signals upon activation by ligand" 15 : 1824-, 2008

      5 Hannun, Y. A, "The Ceramide-centric universe of lipid-mediated cell regulation: stress encounters of the lipid kind" 277 : 25847-, 2002

      6 Wijesinghe, D. S, "Substrate specificity of human ceramide kinase" 46 : 2706-, 2005

      7 Levery, S. B, "Structure elucidation of sphingolipids from the mycopathogen Paracoccidioides brasiliensis: an immunodominant betagalactofuranose residue is carried by a novel glycosylinositol phosphorylceramide antigen" 37 : 8764-, 1998

      8 Hakomori, S. I, "Structure and function of glycosphingolipids and sphingolipids: recollections and future trends" 1780 : 325-, 2008

      9 Zama, K, "Simultaneous quantification of glucosylceramide and galactosylceramide by normal-phase HPLC using O-phtalaldehyde derivatives prepared with sphingolipid ceramide N-deacylase" 19 : 767-, 2009

      10 Zhang, X, "Review: Glycosphingolipids in health and disease" 34 : 3-, 2004

      1 Pewzner-Jung, Y, "When do Lasses (longevity assurance genes) become CerS (ceramide synthases)?: Insights into the regulation of ceramide synthesis" 281 : 25001-, 2006

      2 Tafesse, F. G, "The multigenic sphingomyelin synthase family" 281 : 29421-, 2006

      3 Hakomori, S, "The hapten structure of a developmentally regulated glycolipid antigen (SSEA-1) isolated from human erythrocytes and adenocarcinoma: a preliminary note" 100 : 1578-, 1981

      4 Chakrabandhu, K, "The extracellular glycosphingolipid-binding motif of Fas defines its internalization route, mode and outcome of signals upon activation by ligand" 15 : 1824-, 2008

      5 Hannun, Y. A, "The Ceramide-centric universe of lipid-mediated cell regulation: stress encounters of the lipid kind" 277 : 25847-, 2002

      6 Wijesinghe, D. S, "Substrate specificity of human ceramide kinase" 46 : 2706-, 2005

      7 Levery, S. B, "Structure elucidation of sphingolipids from the mycopathogen Paracoccidioides brasiliensis: an immunodominant betagalactofuranose residue is carried by a novel glycosylinositol phosphorylceramide antigen" 37 : 8764-, 1998

      8 Hakomori, S. I, "Structure and function of glycosphingolipids and sphingolipids: recollections and future trends" 1780 : 325-, 2008

      9 Zama, K, "Simultaneous quantification of glucosylceramide and galactosylceramide by normal-phase HPLC using O-phtalaldehyde derivatives prepared with sphingolipid ceramide N-deacylase" 19 : 767-, 2009

      10 Zhang, X, "Review: Glycosphingolipids in health and disease" 34 : 3-, 2004

      11 Linn, S. C, "Regulation of de novo sphingolipid biosynthesis and the toxic consequences of its disruption" 29 : 831-, 2001

      12 Vance, D. E, "Quantitative determination of the neutral glycosyl ceramides in human blood" 8 : 621-, 1967

      13 Hannun, Y. A, "Principles of bioactive lipid signalling: lessons from sphingolipids" 9 : 139-, 2008

      14 Hoffmann, P, "On the structural diversity of Shiga toxin glycosphingolipid receptors in lymphoid and myeloid cells determined by nanoelectrospray ionization tandem mass spectrometry" 24 : 2295-, 2010

      15 Wheeler, S. F, "Negative ion mass spectrometry of sialylated carbohydrates: discrimination of Nacetylneuraminic acid linkages by MALDI-TOF and ESI-TOF mass spectrometry" 72 : 5027-, 2000

      16 Coetzee, T, "Myelination in the absence of galactocerebroside and sulfatide: normal structure with abnormal function and regional instability" 86 : 209-, 1996

      17 Raas-Rothschild, A, "Glycosphingolipidoses: beyond the enzymatic defect" 21 : 295-, 2004

      18 Yanagisawa, M, "Glycosphingolipid synthesis inhibitor represses cytokine-induced activation of the Ras-MAPK pathway in embryonic neural precursor cells" 138 : 285-, 2005

      19 Ledeen, R. W, "Gangliosides: structure, isolation,and analysis" 83 : 139-, 1982

      20 Causeret, C, "Further characterization of rat dihydroceramide desaturase: tissue distribution, subcellular localization, and substrate specificity" 35 : 1117-, 2000

      21 Schwarz, A, "Distinct roles for ceramide and glucosylceramide at different stages of neuronal growth" 17 : 2929-, 1997

      22 Kannagi, R, "Current relevance of incomplete synthesis and neo-synthesis for cancer-associated alteration of carbohydrate determinants--Hakomori's concepts revisited" 1780 : 525-, 2008

      23 Deshmukh, G. D, "Abnormalities of glycosphingolipid, sulfatide,and ceramide in the polycystic (cpk/cpk) mouse" 35 : 1611-, 1994

      24 Folch, J, "A simple method for the isolation and purification of total lipides from animal tissues" 226 : 497-, 1957

      25 Bligh, E. G, "A rapid method of total lipid extraction and purification" 37 : 911-, 1959

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      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
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      2002-01-01 평가 등재후보학술지 유지 (등재후보1차) KCI등재후보
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.2 0.2 0.22
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.23 0.18 0.403 0.02
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