Literature DB >> 2430918

Multivesicular bodies isolated from rat hepatocytes. Cytochemical evidence for transformation into secondary lysosomes by fusion with primary lysosomes.

E Jost-Vu, R L Hamilton, C A Hornick, J D Belcher, R J Havel.   

Abstract

Plasma lipoproteins (and other ligands) are endocytosed by hepatocytes and appear in multivesicular bodies (MVBs) in the Golgi-lysosome region of the cell prior to their degradation. We have isolated MVB fractions from livers of estradiol-treated rats, permitting studies of their properties (Hornick et al. 1985). Here we report our cytochemical studies of lysosomal enzyme activity in partially and highly purified MVB fractions and in MVBs in hepatocytes in situ. Only about 15% of partially or highly purified MVBs were positive for acid phosphatase and arylsulfatase, consistent with the prelysosomal nature of this compartment. Partially purified MVB fractions contained small round vesicles, 70-120 nm in diameter, which stained intensely for these enzymes; occasionally these vesicles appeared to fuse with MVBs, suggesting that these structures are primary lysosomes. Such stained vesicles were rarely seen in highly purified MVB preparations. Acid phosphatase reaction product with cerium as capture reagent appeared as uniform precipitates surrounding endocytosed plasma lipoproteins in positively stained MVBs. Arylsulfatase reaction product, however, appeared as distinctive arc or plaque-like deposits just inside the MVB-limiting membrane, often in continuity with intense reaction product contained in a fusing primary lysosome. Similar putative primary lysosomes were occasionally observed in isolated, "intact" Golgi fractions from the same livers. Similar histochemical reactivities of MVBs and putative primary lysosomes were observed in thin sections of hepatocytes in situ. These observations support the conclusion that, in hepatocytes, MVBs represent the immediate prelysosomal compartment in the endocytic pathway of macromolecular catabolism, and suggest that MVBs are converted to secondary lysosomes by direct fusion with primary lysosomes arising from closely adjacent Golgi compartments.

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Year:  1986        PMID: 2430918     DOI: 10.1007/bf00508427

Source DB:  PubMed          Journal:  Histochemistry        ISSN: 0301-5564


  25 in total

1.  Increased binding of low density lipoprotein to liver membranes from rats treated with 17 alpha-ethinyl estradiol.

Authors:  P T Kovanen; M S Brown; J L Goldstein
Journal:  J Biol Chem       Date:  1979-11-25       Impact factor: 5.157

2.  Inorganic trimetaphosphatase as a histochemical marker for lysosomes in light and electron microscopy.

Authors:  S B Doty; C E Smith; A R Hand; C Oliver
Journal:  J Histochem Cytochem       Date:  1977-12       Impact factor: 2.479

3.  The cytochemical demonstration of lysosomal aryl sulfatase activity by light and electron microscopy.

Authors:  S Goldfischer
Journal:  J Histochem Cytochem       Date:  1965 Jul-Aug       Impact factor: 2.479

Review 4.  Receptor-mediated endocytosis: concepts emerging from the LDL receptor system.

Authors:  J L Goldstein; M S Brown; R G Anderson; D W Russell; W J Schneider
Journal:  Annu Rev Cell Biol       Date:  1985

5.  Autoradiographic localization of the sites of uptake, cellular transport, and catabolism of low density lipoproteins in the liver of normal and estrogen-treated rats.

Authors:  Y S Chao; A L Jones; G T Hradek; E E Windler; R J Havel
Journal:  Proc Natl Acad Sci U S A       Date:  1981-01       Impact factor: 11.205

6.  Hepatic catabolism of rat and human lipoproteins in rats treated with 17 alpha-ethinyl estradiol.

Authors:  Y S Chao; E E Windler; G C Chen; R J Havel
Journal:  J Biol Chem       Date:  1979-11-25       Impact factor: 5.157

7.  The discovery of lysosomes.

Authors:  D F Bainton
Journal:  J Cell Biol       Date:  1981-12       Impact factor: 10.539

8.  Differentiation of monocytes. Origin, nature, and fate of their azurophil granules.

Authors:  B A Nichols; D F Bainton; M G Farquhar
Journal:  J Cell Biol       Date:  1971-08       Impact factor: 10.539

9.  Uptake of gold- and [3H]cholesteryl linoleate-labeled human low density lipoprotein by cultured rat granulosa cells: cellular mechanisms involved in lipoprotein metabolism and their importance to steroidogenesis.

Authors:  L G Paavola; J F Strauss; C O Boyd; J E Nestler
Journal:  J Cell Biol       Date:  1985-04       Impact factor: 10.539

10.  Receptor-mediated endocytosis of epidermal growth factor by hepatocytes in the perfused rat liver: ligand and receptor dynamics.

Authors:  W A Dunn; A L Hubbard
Journal:  J Cell Biol       Date:  1984-06       Impact factor: 10.539

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  4 in total

1.  Effect of colchicine on lysosomal structures in maturation-ameloblasts of the rat incisor.

Authors:  A H Salama; D R Eisenmann; A E Zaki
Journal:  Cell Tissue Res       Date:  1990-05       Impact factor: 5.249

2.  Isolation and characterization of three endosomal fractions from the liver of estradiol-treated rats.

Authors:  J D Belcher; R L Hamilton; S E Brady; C A Hornick; S Jaeckle; W J Schneider; R J Havel
Journal:  Proc Natl Acad Sci U S A       Date:  1987-10       Impact factor: 11.205

3.  Identification and distribution of proteins in isolated endosomal fractions of rat liver: involvement in endocytosis, recycling and transcytosis.

Authors:  A Pol; D Ortega; C Enrich
Journal:  Biochem J       Date:  1997-04-15       Impact factor: 3.857

4.  The cytoplasmic domain mediates localization of furin to the trans-Golgi network en route to the endosomal/lysosomal system.

Authors:  H Bosshart; J Humphrey; E Deignan; J Davidson; J Drazba; L Yuan; V Oorschot; P J Peters; J S Bonifacino
Journal:  J Cell Biol       Date:  1994-09       Impact factor: 10.539

  4 in total

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