Literature DB >> 7618436

Sphingolipid activator proteins in the neuronal ceroid-lipofuscinoses: an immunological study.

J Tyynelä1, M Baumann, M Henseler, K Sandhoff, M Haltia.   

Abstract

The molecular defects underlying neuronal ceroid-lipofuscinoses (NCL) are still unknown. However, more data exist on the composition of the hydrophobic storage material characteristic of NCL. Accumulation of subunit c of the mitochondrial ATP synthase has been shown in most forms of human NCL with the exception of the infantile NCL (INCL) for which we have recently demonstrated storage of sphingolipid activator proteins (SAP). In the present study we raised an antiserum against storage cytosomes purified from INCL brain. Using the anti-INCL antiserum and monospecific SAP antisera, we studied storage material isolated from the brains of patients affected with NCL by Western analysis, and found a 12-kDa protein showing a SAP-like immunoreactivity not only in INCL, but also in all the childhood forms of NCL. Furthermore, using the anti-sap-D antiserum for immunohistochemistry, we observed strong immunoreactivity of the storage cytosomes in all major forms of NCL, and also in tissues of non-neuroectodermal origin. From these data we conclude that the presence of SAP within the storage bodies is a phenomenon common to all major forms of human NCL.

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Year:  1995        PMID: 7618436     DOI: 10.1007/BF00307641

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  35 in total

1.  A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples.

Authors:  M A Markwell; S M Haas; L L Bieber; N E Tolbert
Journal:  Anal Biochem       Date:  1978-06-15       Impact factor: 3.365

2.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

3.  [A cerebrosidesulfatase from swine kidney].

Authors:  E Mehl; H Jatzkewitz
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1964

4.  A variant of Jansky-Bielschowsky disease.

Authors:  P Santavuori; J Rapola; K Sainio; C Raitta
Journal:  Neuropediatrics       Date:  1982-08       Impact factor: 1.947

5.  Glycosphingolipid specificity of the human sulfatide activator protein.

Authors:  A Vogel; G Schwarzmann; K Sandhoff
Journal:  Eur J Biochem       Date:  1991-09-01

6.  Mutational analysis in a patient with a variant form of Gaucher disease caused by SAP-2 deficiency.

Authors:  M A Rafi; G de Gala; X L Zhang; D A Wenger
Journal:  Somat Cell Mol Genet       Date:  1993-01

7.  Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common gene.

Authors:  D Schnabel; M Schröder; W Fürst; A Klein; R Hurwitz; T Zenk; J Weber; K Harzer; B C Paton; A Poulos
Journal:  J Biol Chem       Date:  1992-02-15       Impact factor: 5.157

8.  Batten disease: past, present, and future.

Authors:  J A Rider; D L Rider
Journal:  Am J Med Genet Suppl       Date:  1988

9.  Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis.

Authors:  J Tyynelä; D N Palmer; M Baumann; M Haltia
Journal:  FEBS Lett       Date:  1993-09-06       Impact factor: 4.124

10.  Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis).

Authors:  N A Hall; B D Lake; N N Dewji; A D Patrick
Journal:  Biochem J       Date:  1991-04-01       Impact factor: 3.857

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  7 in total

Review 1.  Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses.

Authors:  Sara E Mole; Ruth E Williams; Hans H Goebel
Journal:  Neurogenetics       Date:  2005-09-28       Impact factor: 2.660

2.  Accumulation of sphingolipid activator proteins (SAPs) A and D in granular osmiophilic deposits in miniature Schnauzer dogs with ceroid-lipofuscinosis.

Authors:  D N Palmer; J Tyynelä; H C van Mil; V J Westlake; R D Jolly
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

3.  A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration.

Authors:  J Tyynelä; I Sohar; D E Sleat; R M Gin; R J Donnelly; M Baumann; M Haltia; P Lobel
Journal:  EMBO J       Date:  2000-06-15       Impact factor: 11.598

4.  The juvenile Batten disease protein, CLN3, and its role in regulating anterograde and retrograde post-Golgi trafficking.

Authors:  Susan L Cotman; John F Staropoli
Journal:  Clin Lipidol       Date:  2012-02

5.  Recent advances in the molecular genetics of the neuronal ceroid lipofuscinoses.

Authors:  S E Mole
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

6.  Aberrant upregulation of the glycolytic enzyme PFKFB3 in CLN7 neuronal ceroid lipofuscinosis.

Authors:  Irene Lopez-Fabuel; Marina Garcia-Macia; Costantina Buondelmonte; Olga Burmistrova; Nicolo Bonora; Paula Alonso-Batan; Brenda Morant-Ferrando; Carlos Vicente-Gutierrez; Daniel Jimenez-Blasco; Ruben Quintana-Cabrera; Emilio Fernandez; Jordi Llop; Pedro Ramos-Cabrer; Aseel Sharaireh; Marta Guevara-Ferrer; Lorna Fitzpatrick; Christopher D Thompton; Tristan R McKay; Stephan Storch; Diego L Medina; Sara E Mole; Peter O Fedichev; Angeles Almeida; Juan P Bolaños
Journal:  Nat Commun       Date:  2022-01-27       Impact factor: 17.694

7.  Neuronal ceroid lipofuscinosis in the Russian population: Two novel mutations and the prevalence of heterozygous carriers.

Authors:  Anastasiya A Kozina; Elena G Okuneva; Natalia V Baryshnikova; Olga B Kondakova; Ekaterina A Nikolaeva; Inessa D Fedoniuk; Svetlana V Mikhailova; Anna Y Krasnenko; Ivan F Stetsenko; Nikolay A Plotnikov; Olesia I Klimchuk; Yaroslav V Popov; Ekaterina I Surkova; Peter A Shatalov; Alexander S Rakitko; Valery V Ilinsky
Journal:  Mol Genet Genomic Med       Date:  2020-05-15       Impact factor: 2.473

  7 in total

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