Literature DB >> 4075230

Triacylglycerol as a precursor in phospholipid biosynthesis in cultured neuroblastoma cells: studies with labeled glucose, fatty acid, and triacylglycerol.

H W Cook, M W Spence.   

Abstract

Neuroblastoma cells rapidly incorporate exogenous fatty acids into cellular triacylglycerol and relationships between triacylglycerol and phospholipid biosynthesis have been indicated by the relative time course of labeling of these lipids. To evaluate this further, neuroblastoma cells were labeled using potential precursors of phospholipid including radiolabeled triacyglycerol, glycerol, glucose, and fatty acid. With [2-3H]glycerol or a mixture of [2-3H]glycerol trioleate and glycerol tri[1-14C]oleate, phospholipids were labeled at very low levels (less than 0.1 and less than 0.5%, respectively). With [6-3H]glucose, labeling of lipids (0.5-3.5%) was greatest in medium containing 19 mM fructose, whereas labeling with [1-14C]18:2(n-6) was similar in media containing either 19 mM fructose or 25 mM glucose. Labeling of the glycerol moiety of triacylglycerol with [6-3H]glucose increased with 40-200 microM 18:2(n-6) present and occurred predominantly in 2 h. Some [6-3H]glucose label was in fatty acyl chains (chiefly 16:0) of triacylglycerol by 16 h, but was unaffected by exogenous 18:2(n-6). Triacylglycerol was the only lipid to increase in mass (threefold with 200 microM 18:2(n-6)). During the chase of cells pulsed with [6-3H]glucose, label in triacylglycerol declined within 0.5 h, whereas in phospholipid it increased transiently up to 2 h and then declined. Changes were inversely proportional to 18:2(n-6) levels in the chase medium and labeled acyl chains moved in parallel with the glycerol moiety. Thus, a major portion of acyl chain transfer from triacylglycerol was accompanied by glycerol.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1985        PMID: 4075230     DOI: 10.1139/o85-114

Source DB:  PubMed          Journal:  Can J Biochem Cell Biol        ISSN: 0714-7511


  7 in total

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Authors:  Sona Rajakumari; Günther Daum
Journal:  J Biol Chem       Date:  2010-03-23       Impact factor: 5.157

2.  IDENTIFYING CANCER SPECIFIC METABOLIC SIGNATURES USING CONSTRAINT-BASED MODELS.

Authors:  A Schultz; S Mehta; C W Hu; F W Hoff; T M Horton; S M Kornblau; A A Qutub
Journal:  Pac Symp Biocomput       Date:  2017

3.  Uptake and incorporation of docosahexaenoic acid (DHA) into neuronal cell body and neurite/nerve growth cone lipids: evidence of compartmental DHA metabolism in nerve growth factor-differentiated PC12 cells.

Authors:  R E Martin; J Q Wickham; A S Om; J Sanders; N Ceballos
Journal:  Neurochem Res       Date:  2000-05       Impact factor: 3.996

4.  Cell-specific fatty acylation of proteins in cultured cells of neuronal and glial origin.

Authors:  D M Byers; H W Cook; F B Palmer; M W Spence
Journal:  Neurochem Res       Date:  1989-06       Impact factor: 3.996

5.  Lipidomic analyses reveal enhanced lipolysis in planthoppers feeding on resistant host plants.

Authors:  Xiaohong Zheng; Yeyun Xin; Yaxin Peng; Junhan Shan; Ning Zhang; Di Wu; Jianping Guo; Jin Huang; Wei Guan; Shaojie Shi; Cong Zhou; Rongzhi Chen; Bo Du; Lili Zhu; Fang Yang; Xiqin Fu; Longping Yuan; Guangcun He
Journal:  Sci China Life Sci       Date:  2020-11-05       Impact factor: 6.038

6.  Metabolism of n-6 fatty acids by NIH-3T3 cells transfected with the ras oncogene.

Authors:  R J de Antueno; R C Cantrill; Y S Huang; G W Ells; M Elliot; D F Horrobin
Journal:  Mol Cell Biochem       Date:  1994-10-12       Impact factor: 3.396

7.  Arachidonic acid uptake by phospholipids and triacylglycerols of rat brain subcellular membranes.

Authors:  T N Lin; R MacQuarrie; G Y Sun
Journal:  Lipids       Date:  1988-10       Impact factor: 1.880

  7 in total

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