Literature DB >> 6438392

Dolichol metabolism in cultured skin fibroblasts from patients with "neuronal" ceroid lipofuscinosis (Batten's disease).

B C Paton, A Poulos.   

Abstract

Dolichol metabolism was investigated in skin fibroblast cultures from normal individuals and patients with Batten's disease. Incorporation of [3H]mevalonolactone and [14C]acetate into the dolichol fraction of total lipid extracts was similar in cells from normal individuals and patients with Batten's disease. [14C]Acetate incorporation into dolichol in non-saponifiable lipid extracts was compared with incorporation into dolichol in total lipid extracts, and no difference in the proportion of dolichol esterified to fatty acids was found in Batten's cells as compared to normal cells. The rate of loss of radioactivity from the dolichol pool after prelabelling with [14C]acetate was also similar in cells from Batten's and normal individuals. Thus, in the fibroblast system used, no evidence was found to support the hypothesis that Batten's disease is due to a defect in dolichol metabolism.

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Year:  1984        PMID: 6438392     DOI: 10.1007/bf01801766

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  32 in total

1.  Diagnostic significance of myeloperoxidase assay in neuronal ceroid-lipofuscinoses (Batten-Vogt syndrome).

Authors:  H Pilz; G Schwendemann; H H Goebel
Journal:  Neurology       Date:  1978-09       Impact factor: 9.910

2.  Specific involvement of muscle, nerve, and skin in late infantile and juvenile amaurotic idiocy.

Authors:  S Carpenter; G Karpati; F Andermann
Journal:  Neurology       Date:  1972-02       Impact factor: 9.910

3.  Presidential address: Studies in the neuronal ceroid-lipofuscinoses.

Authors:  W Zeman
Journal:  J Neuropathol Exp Neurol       Date:  1974-01       Impact factor: 3.685

4.  A dominant form of neuronal ceroid-lipofuscinosis.

Authors:  D H Boehme; J C Cottrell; S C Leonberg; W Zeman
Journal:  Brain       Date:  1971       Impact factor: 13.501

5.  Late infantile progressive encephalopathy with disturbed poly-unsaturated fat metabolism.

Authors:  B Hagberg; P Sourander; L Svennerholm
Journal:  Acta Paediatr Scand       Date:  1968-11

6.  [Anomalies in fatty acids distribution and superoxide dismutase activity in lymphocytes of an adult with atypical ceroid lipofuscinosis].

Authors:  L Rumbach; J M Warter; G Coquillat; C Marescaux; M Collard; F Rohmer; R Bieth; R Zawislak
Journal:  Rev Neurol (Paris)       Date:  1983       Impact factor: 2.607

7.  Polyunsaturated fatty acid lipidosis. II. Lipid biochemical studies.

Authors:  L Svennerholm; B Hagberg; M Haltia; P Sourander; M T Vanier
Journal:  Acta Paediatr Scand       Date:  1975-05

8.  Dolichols in brain and urinary sediment in neuronal ceroid lipofuscinosis.

Authors:  L S Wolfe; N M Ng Ying Kin; J Palo; M Haltia
Journal:  Neurology       Date:  1983-01       Impact factor: 9.910

9.  Accumulation of dolichols in brains of elderly.

Authors:  R K Pullarkat; H Reha
Journal:  J Biol Chem       Date:  1982-06-10       Impact factor: 5.157

10.  High levels of brain dolichols in neuronal ceroid-lipofuscinosis and senescence.

Authors:  N M Ng Ying Kin; J Palo; M Haltia; L S Wolfe
Journal:  J Neurochem       Date:  1983-05       Impact factor: 5.372

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  2 in total

1.  Mevalonic aciduria: pathobiochemical effects of mevalonate kinase deficiency on cholesterol metabolism in intact fibroblasts.

Authors:  G Hoffmann; K M Gibson; W L Nyhan; L Sweetman
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

2.  Normal dolichol concentration in urine sediments from four patients with neuronal ceroid lipofuscinosis (Batten's disease).

Authors:  B C Paton; A Poulos
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

  2 in total

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