Literature DB >> 7122633

Pathology of the Gaucher cell.

J L Parkin, R D Brunning.   

Abstract

The Gaucher cell results from the accumulation of excessive glucocerebroside in cells of the monocyte-macrophage system. It is characterized ultrastructurally by the presence of cytoplasmic inclusions which consist of tubule-like structures measuring 130 to 150 Ao in diameter. Utilizing freeze fracture and x-ray diffraction techniques these structures appear to be bilayers measuring 6 nm in thickness, 40 to 60 nm wide and up to 600 nm in length. The Gaucher cell contains isoenzyme 5 of acid phosphatase which is resistant to prior incubation in tartaric acid. The bone marrow smears from patients with Gaucher's disease contain monocytes and monocytoid cells which contain inclusions which are acid phosphatase positive and resemble the acid phosphatase positive inclusions in the Gaucher cells. Ultrastructural studies of monocytes from Gaucher patients demonstrated membrane-bound inclusions containing tubule-like structures identical to those in Gaucher cells. These monocytic cells appear to represent precursors of Gaucher cells.

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Year:  1982        PMID: 7122633

Source DB:  PubMed          Journal:  Prog Clin Biol Res        ISSN: 0361-7742


  12 in total

1.  Photo Essay: Retinal Changes in Type 3 Gaucher Disease.

Authors:  Shweta Anand; Desmond Kidd; Derralynn Hughes
Journal:  Neuroophthalmology       Date:  2018-02-05

2.  Gaucher Disease-Induced Pluripotent Stem Cells Display Decreased Erythroid Potential and Aberrant Myelopoiesis.

Authors:  Judi A Sgambato; Tea Soon Park; Diana Miller; Leelamma M Panicker; Ellen Sidransky; Yu Lun; Ola Awad; Søren M Bentzen; Elias T Zambidis; Ricardo A Feldman
Journal:  Stem Cells Transl Med       Date:  2015-06-10       Impact factor: 6.940

3.  Biotherapeutic target or sink: analysis of the macrophage mannose receptor tissue distribution in murine models of lysosomal storage diseases.

Authors:  Xin Sheen Zhang; William Brondyk; John T Lydon; Beth L Thurberg; Peter A Piepenhagen
Journal:  J Inherit Metab Dis       Date:  2011-03-17       Impact factor: 4.982

4.  Alleles with more than one mutation can complicate genotype/phenotype studies in Mendelian disorders: Lessons from Gaucher disease.

Authors:  Shahzeb Hassan; Grisel Lopez; Barbara K Stubblefield; Nahid Tayebi; Ellen Sidransky
Journal:  Mol Genet Metab       Date:  2018-06-28       Impact factor: 4.797

Review 5.  Type 2 Gaucher disease: phenotypic variation and genotypic heterogeneity.

Authors:  N Gupta; I M Oppenheim; E F Kauvar; N Tayebi; E Sidransky
Journal:  Blood Cells Mol Dis       Date:  2010-09-28       Impact factor: 3.039

6.  Gaucher disease: genetic heterogeneity within and among the subtypes detected by immunoblotting.

Authors:  D Fabbro; R J Desnick; G A Grabowski
Journal:  Am J Hum Genet       Date:  1987-01       Impact factor: 11.025

7.  MR imaging in adults with Gaucher disease type I: evaluation of marrow involvement and disease activity.

Authors:  G Hermann; R S Shapiro; I F Abdelwahab; G Grabowski
Journal:  Skeletal Radiol       Date:  1993       Impact factor: 2.199

8.  Posttranslational processing of human lysosomal acid beta-glucosidase: a continuum of defects in Gaucher disease type 1 and type 2 fibroblasts.

Authors:  J E Bergmann; G A Grabowski
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

Review 9.  Glucocerebrosidase and its relevance to Parkinson disease.

Authors:  Jenny Do; Cindy McKinney; Pankaj Sharma; Ellen Sidransky
Journal:  Mol Neurodegener       Date:  2019-08-29       Impact factor: 14.195

10.  Reduced glucocerebrosidase activity in monocytes from patients with Parkinson's disease.

Authors:  Farzaneh Atashrazm; Deborah Hammond; Gayathri Perera; Carol Dobson-Stone; Nicole Mueller; Russell Pickford; Woojin Scott Kim; John B Kwok; Simon J G Lewis; Glenda M Halliday; Nicolas Dzamko
Journal:  Sci Rep       Date:  2018-10-18       Impact factor: 4.379

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