Literature DB >> 3160696

Synthesis and transport of lysosomal acid phosphatase in normal and I-cell fibroblasts.

P Lemansky, V Gieselmann, A Hasilik, K von Figura.   

Abstract

The biosynthesis, proteolytic processing, and transport of lysosomal acid phosphatase in normal and I-cell human skin fibroblasts was studied by metabolic labeling of the cells and isolation of acid phosphatase by immunoprecipitation. Several forms of the enzyme were identified in pulse-chase experiments. The largest precursor form had a Mr of 110,000. It was accompanied by several smaller polypeptides (Mr = 84,000-62,000), which were localized to light membranes containing the markers of endoplasmic reticulum and Golgi complex. These polypeptides were further processed to mature forms with apparent Mr of 57,000, 48,000, and 43,000 that accumulated in the cells and were associated with dense lysosomes. Less than 10% of newly synthesized acid phosphatase was secreted mainly as Mr = 112,000 and 74,000 forms. The processing of acid phosphatase was inhibited by NH4Cl and by a peptidyldiazomethyl ketone inhibitor of cysteine proteinases. The intracellular Mr = 110,000, 57,000, and 48,000 and the secreted Mr = 112,000 and 64,000 forms contained phosphorylated oligosaccharides cleavable by endo-beta-N-acetylglucosaminidase H. Transport of acid phosphatase into lysosomes was sensitive to NH4Cl and dependent on mannose 6-phosphate specific receptors by the following criteria: (i) inhibition of endocytosis of acid phosphatase by mannose 6-phosphate, (ii) enhancement of the secretion of acid phosphatase in the presence of antibodies to the mannose 6-phosphatase specific receptor, and (iii) secretion of about two-thirds of newly synthesized acid phosphatase in I-cell fibroblasts. Obviously, the mechanism of transport of acid phosphatase into lysosomes is indistinguishable from that operating for other lysosomal enzymes in fibroblasts. In contrast to other lysosomal enzymes, acid phosphatase appears to be subjected to an early proteolytic processing, presumably within the endoplasmic reticulum, which results in secretion of several processed forms of the enzyme.

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Year:  1985        PMID: 3160696

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  15 in total

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Authors:  A D Agyei; I V Herbert; N W Runham
Journal:  Parasitol Res       Date:  1991       Impact factor: 2.289

2.  Inhibitor studies indicate that active cathepsin L is probably essential to its own processing in cultured fibroblasts.

Authors:  A Salminen; M M Gottesman
Journal:  Biochem J       Date:  1990-11-15       Impact factor: 3.857

3.  Mannose 6 dephosphorylation of lysosomal proteins mediated by acid phosphatases Acp2 and Acp5.

Authors:  Georgia Makrypidi; Markus Damme; Sven Müller-Loennies; Maria Trusch; Bernhard Schmidt; Hartmut Schlüter; Joerg Heeren; Torben Lübke; Paul Saftig; Thomas Braulke
Journal:  Mol Cell Biol       Date:  2011-12-12       Impact factor: 4.272

4.  Cellular Uptake and Delivery of Myeloperoxidase to Lysosomes Promote Lipofuscin Degradation and Lysosomal Stress in Retinal Cells.

Authors:  Gouri Yogalingam; Amanda R Lee; Donald S Mackenzie; Travis J Maures; Agnes Rafalko; Heather Prill; Geoffrey Y Berguig; Chuck Hague; Terri Christianson; Sean M Bell; Jonathan H LeBowitz
Journal:  J Biol Chem       Date:  2017-01-23       Impact factor: 5.157

5.  Synthesis of a truncated Mr 46,000 mannose 6-phosphate receptor that is secreted and retains ligand binding.

Authors:  M Wendland; A Hille; G Nagel; A Waheed; K von Figura; R Pohlmann
Journal:  Biochem J       Date:  1989-05-15       Impact factor: 3.857

6.  The biochemical diagnosis of lysosomal storage diseases--a review of five years experience.

Authors:  I J Wallace; C A McCusker; D McCormick
Journal:  Ir J Med Sci       Date:  1990-07       Impact factor: 1.568

7.  Restoration of arylsulphatase B activity in human mucopolysaccharidosis-type-VI fibroblasts by retroviral-vector-mediated gene transfer.

Authors:  C Peters; W Rommerskirch; S Modaressi; K von Figura
Journal:  Biochem J       Date:  1991-06-01       Impact factor: 3.857

8.  Targeting of a lysosomal membrane protein: a tyrosine-containing endocytosis signal in the cytoplasmic tail of lysosomal acid phosphatase is necessary and sufficient for targeting to lysosomes.

Authors:  C Peters; M Braun; B Weber; M Wendland; B Schmidt; R Pohlmann; A Waheed; K von Figura
Journal:  EMBO J       Date:  1990-11       Impact factor: 11.598

9.  Human lysosomal acid phosphatase: cloning, expression and chromosomal assignment.

Authors:  R Pohlmann; C Krentler; B Schmidt; W Schröder; G Lorkowski; J Culley; G Mersmann; C Geier; A Waheed; S Gottschalk
Journal:  EMBO J       Date:  1988-08       Impact factor: 11.598

10.  Human lysosomal acid phosphatase is transported as a transmembrane protein to lysosomes in transfected baby hamster kidney cells.

Authors:  A Waheed; S Gottschalk; A Hille; C Krentler; R Pohlmann; T Braulke; H Hauser; H Geuze; K von Figura
Journal:  EMBO J       Date:  1988-08       Impact factor: 11.598

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