Literature DB >> 4001945

Defect in vitamin B12 release from lysosomes: newly described inborn error of vitamin B12 metabolism.

D S Rosenblatt, A Hosack, N V Matiaszuk, B A Cooper, R Laframboise.   

Abstract

Cultured diploid fibroblasts from a patient with a previously undescribed inborn error of cobalamin metabolism accumulate unmetabolized, nonprotein-bound vitamin B12 in lysosomes. These cells are able to endocytose the transcobalamin II-B12 complex and to release B12 from transcobalamin II. The freed vitamin B12 is not released from lysosomes into the cytoplasm of the cell. This suggests that there is a specific lysosomal transport mechanism for vitamin B12 in the human.

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Year:  1985        PMID: 4001945     DOI: 10.1126/science.4001945

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  34 in total

1.  Clinical and biochemical observations in a patient with combined Pompe disease and cblC mutation.

Authors:  F A Wijburg; D S Rosenblatt; G D Vos; J W Oorthuys; L G van't Hek; B J Poorthuis; M K Sanders; R B Schutgens
Journal:  Eur J Pediatr       Date:  1992-02       Impact factor: 3.183

Review 2.  Insights into lysosomal cobalamin trafficking: lessons learned from cblF disease.

Authors:  Susann Gailus; Wolfgang Höhne; Bruno Gasnier; Peter Nürnberg; Brian Fowler; Frank Rutsch
Journal:  J Mol Med (Berl)       Date:  2010-02-20       Impact factor: 4.599

Review 3.  Lysosomal membrane proteomics and biogenesis of lysosomes.

Authors:  Richard D Bagshaw; Don J Mahuran; John W Callahan
Journal:  Mol Neurobiol       Date:  2005-08       Impact factor: 5.590

Review 4.  Age-related lysosomal dysfunction: an unrecognized roadblock for cobalamin trafficking?

Authors:  Hua Zhao; Ulf T Brunk; Brett Garner
Journal:  Cell Mol Life Sci       Date:  2011-10-21       Impact factor: 9.261

Review 5.  Molecular physiology and pathophysiology of lysosomal membrane transporters.

Authors:  C Sagné; B Gasnier
Journal:  J Inherit Metab Dis       Date:  2008-04-15       Impact factor: 4.982

Review 6.  Navigating the B(12) road: assimilation, delivery, and disorders of cobalamin.

Authors:  Carmen Gherasim; Michael Lofgren; Ruma Banerjee
Journal:  J Biol Chem       Date:  2013-03-28       Impact factor: 5.157

7.  Failure of lysosomal release of vitamin B12: a new complementation group causing methylmalonic aciduria (cblF).

Authors:  D Watkins; D S Rosenblatt
Journal:  Am J Hum Genet       Date:  1986-09       Impact factor: 11.025

8.  Processing of alkylcobalamins in mammalian cells: A role for the MMACHC (cblC) gene product.

Authors:  Luciana Hannibal; Jihoe Kim; Nicola E Brasch; Sihe Wang; David S Rosenblatt; Ruma Banerjee; Donald W Jacobsen
Journal:  Mol Genet Metab       Date:  2009-04-16       Impact factor: 4.797

Review 9.  Genetic disorders of vitamin B₁₂ metabolism: eight complementation groups--eight genes.

Authors:  D Sean Froese; Roy A Gravel
Journal:  Expert Rev Mol Med       Date:  2010-11-29       Impact factor: 5.600

10.  Defective glucuronic acid transport from lysosomes of infantile free sialic acid storage disease fibroblasts.

Authors:  H J Blom; H C Andersson; R Seppala; F Tietze; W A Gahl
Journal:  Biochem J       Date:  1990-06-15       Impact factor: 3.857

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