Literature DB >> 662919

Receptor-mediated uptake of lysosomal enzymes.

W S Sly, A Kaplan, D T Achord, F E Brot, C E Bell.   

Abstract

This paper reviews the evidence for two different forms of carbohydrate-mediated recognition of lysosomal enzymes by cell surface receptors. The recognition marker on lysosomal enzymes which are rapidly pinocytosed by fibroblasts contains phosphate, probably linked to D-mannose as a phosphomannosyl moiety. The fraction of lysosomal hydrolases bearing this recognition marker for fibroblasts varies, depending on the tissue source. Another form of recognition accounts for rapid plasma clearance of infused lysosomal enzymes in the rat. This rapid clearance is mediated by receptors on Kupffer cells and other reticuloendothelial cells that recognize mannosyl residues on the glycoprotein hydrolases.

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Year:  1978        PMID: 662919

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


  6 in total

Review 1.  Lysosomal storage diseases.

Authors:  Frances M Platt; Alessandra d'Azzo; Beverly L Davidson; Elizabeth F Neufeld; Cynthia J Tifft
Journal:  Nat Rev Dis Primers       Date:  2018-10-01       Impact factor: 52.329

Review 2.  Management of non-neuronopathic Gaucher disease with special reference to pregnancy, splenectomy, bisphosphonate therapy, use of biomarkers and bone disease monitoring.

Authors:  T M Cox; J M F G Aerts; N Belmatoug; M D Cappellini; S vom Dahl; J Goldblatt; G A Grabowski; C E M Hollak; P Hwu; M Maas; A M Martins; P K Mistry; G M Pastores; A Tylki-Szymanska; J Yee; N Weinreb
Journal:  J Inherit Metab Dis       Date:  2008-05-23       Impact factor: 4.982

3.  Characterization of the complex formed by β-glucocerebrosidase and the lysosomal integral membrane protein type-2.

Authors:  Friederike Zunke; Lisa Andresen; Sophia Wesseler; Johann Groth; Philipp Arnold; Michelle Rothaug; Joseph R Mazzulli; Dimitri Krainc; Judith Blanz; Paul Saftig; Michael Schwake
Journal:  Proc Natl Acad Sci U S A       Date:  2016-03-21       Impact factor: 11.205

4.  Enhanced delivery of α-glucosidase for Pompe disease by ICAM-1-targeted nanocarriers: comparative performance of a strategy for three distinct lysosomal storage disorders.

Authors:  Janet Hsu; Laura Northrup; Tridib Bhowmick; Silvia Muro
Journal:  Nanomedicine       Date:  2011-09-09       Impact factor: 5.307

5.  Using Bibliometric Analysis and Machine Learning to Identify Compounds Binding to Sialidase-1.

Authors:  Jennifer J Klein; Nancy C Baker; Daniel H Foil; Kimberley M Zorn; Fabio Urbina; Ana C Puhl; Sean Ekins
Journal:  ACS Omega       Date:  2021-01-20

6.  Human recombinant lysosomal β-Hexosaminidases produced in Pichia pastoris efficiently reduced lipid accumulation in Tay-Sachs fibroblasts.

Authors:  Angela J Espejo-Mojica; Alexander Rodríguez-López; Rong Li; Wei Zheng; Carlos J Alméciga-Díaz; Cindy Dulcey-Sepúlveda; Germán Combariza; Luis A Barrera
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-10-27       Impact factor: 3.359

  6 in total

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