Literature DB >> 3939596

A method for enrichment of hybrid somatic cells: complementation studies in certain lysosomal enzymopathies.

P V Nelson, W F Carey.   

Abstract

An improved method, which combined a number of published techniques, is described for the polyethylene-glycol-induced fusion of mononuclear human skin fibroblasts in the presence of phytohaemagglutinin-P and for the subsequent isolation of polynuclear cells by Ficoll gradient sedimentation. Enriched cultures contain between 60 and 75% multinucleated cells and may be maintained in culture without fetal calf serum for up to 14 days without significant overgrowth by the few contaminating mononuclear parental cells. Complementation appears not to occur between GM1 gangliosidosis and mucopolysaccharidosis, type VI B (Morquio) cell strains; this experimental observation provides support for the earlier hypothesis that the mutations for these conditions are allelic. Earlier observations that complementation does not occur between selected phenotypic variants (viz., neuronopathic forms and those without neurological involvement) of sphingomyelin storage (Niemann-Pick) disease or Gaucher's disease are confirmed.

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Year:  1985        PMID: 3939596     DOI: 10.1007/bf01819286

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


  16 in total

1.  Phytohemagglutinin enhancement of cell fusion reduces polyethylene glycol cytotoxicity.

Authors:  W E Mercer; R A Schlegel
Journal:  Exp Cell Res       Date:  1979-05       Impact factor: 3.905

2.  Early alterations in amino acid pools and protein synthesis of diploid fibroblasts stimulated to synthesize DNA by addition of serum.

Authors:  F Wiebel; R Baserga
Journal:  J Cell Physiol       Date:  1969-10       Impact factor: 6.384

3.  Mucolipidosis I: increased sialic acid content and deficiency of an alpha-N-acetylneuraminidase in cultured fibroblasts.

Authors:  M Cantz; J Gehler; J Spranger
Journal:  Biochem Biophys Res Commun       Date:  1977-01-24       Impact factor: 3.575

4.  Enzymatic diagnosis of the mucopolysaccharidoses: experience of 96 cases diagnosed in a five-year period.

Authors:  J J Hopwood; V Muller; J R Harrison; W F Carey; H Elliott; E F Robertson; A C Pollard
Journal:  Med J Aust       Date:  1982-03-20       Impact factor: 7.738

5.  Enzymatic activities on purine pyrimidine metabolism in nine mycoplasma species contaminating cell cultures.

Authors:  M Hamet; C Bonissol; P Cartier
Journal:  Clin Chim Acta       Date:  1980-04-11       Impact factor: 3.786

6.  Enrichment of human heterokaryons by Ficoll gradient for complementation analysis of iduronate sulfatase deficiency.

Authors:  L R Eisenberg; B R Migeon
Journal:  Somatic Cell Genet       Date:  1979-11

7.  Mutations of glucocerebrosidase: discrimination of neurologic and non-neurologic phenotypes of Gaucher disease.

Authors:  E I Ginns; R O Brady; S Pirruccello; C Moore; S Sorrell; F S Furbish; G J Murray; J Tager; J A Barranger
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

8.  Enzymological diagnosis of a group of lysosomal storage diseases. Review of 5-year experience of 1600 patient-sample referrals.

Authors:  A C Pollard; W F Carey; P V Nelson; A Poulos; G N Hill
Journal:  Med J Aust       Date:  1980-11-15       Impact factor: 7.738

9.  Rapid clonal growth and serial passage of human diploid fibroblasts in a lipid-enriched synthetic medium supplemented with epidermal growth factor, insulin, and dexamethasone.

Authors:  W J Bettger; S T Boyce; B J Walthall; R G Ham
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

10.  Correction of I-cell defect by hybridization with lysosomal enzyme deficient human fibroblasts.

Authors:  A d'Azzo; D J Halley; A Hoogeveen; H Galjaard
Journal:  Am J Hum Genet       Date:  1980-07       Impact factor: 11.025

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  6 in total

1.  Genetic complementation analysis of mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency in cultured fibroblasts.

Authors:  O Søvik; J M Saudubray; A Munnich; L Sweetman
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders.

Authors:  B T Poll-The; O H Skjeldal; O Stokke; A Poulos; F Demaugre; J M Saudubray
Journal:  Hum Genet       Date:  1989-01       Impact factor: 4.132

3.  Mucolipidosis IV consists of one complementation group.

Authors:  E Goldin; A Cooney; C R Kaneski; R O Brady; R Schiffmann
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-20       Impact factor: 11.205

4.  Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.

Authors:  Y Suzuki; N Shimozawa; S Yajima; S Tomatsu; N Kondo; Y Nakada; S Akaboshi; M Lai; Y Tanabe; T Hashimoto
Journal:  Am J Hum Genet       Date:  1994-01       Impact factor: 11.025

5.  Genetic heterogeneity in Niemann-Pick C disease: a study using somatic cell hybridization and linkage analysis.

Authors:  M T Vanier; S Duthel; C Rodriguez-Lafrasse; P Pentchev; E D Carstea
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

6.  Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects.

Authors:  B C Paton; P C Sharp; D I Crane; A Poulos
Journal:  J Clin Invest       Date:  1996-02-01       Impact factor: 14.808

  6 in total

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