Literature DB >> 3943118

Evidence for a decreased membrane recycling in the cells of renal proximal tubules exposed to high concentrations of ferritin.

E I Christensen.   

Abstract

The present study was performed to investigate whether membrane recycling via the dense apical tubules in cells of renal proximal tubules could be modified after exposure to large amounts of cationized ferritin. Proximal tubules in the rat kidney were microinfused in vivo with cationized ferritin for 10 or 30 min and then fixed with glutaraldehyde by microinfusion, or proximal tubules were microinfused with ferritin for 30 min and then fixed 2 h thereafter. The tubules were processed for electron microscopy, and the surface density and the volume density of the different cell organelles involved in endocytosis were determined by morphometry. The morphometric analyses showed that after loading of the endocytic vesicles with ferritin the surface density of dense apical tubules decreased to about 50% of the original value. However, 2 h later when ferritin had accumulated in the lysosomes the surface density of dense apical tubules had returned to control values. Furthermore, cationized ferritin was virtually absent from the Golgi region, indicating that the Golgi apparatus in these cells does not participate in membrane recycling. In conclusion, the present study shows that membrane recycling in renal proximal tubule cells can in part be inhibited by loading the endocytic vacuoles with ferritin.

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Year:  1986        PMID: 3943118     DOI: 10.1007/bf00221857

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  19 in total

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Journal:  Annu Rev Biochem       Date:  1977       Impact factor: 23.643

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Review 5.  Membrane recycling in secretory cells: implications for traffic of products and specialized membranes within the Golgi complex.

Authors:  M G Farquhar
Journal:  Methods Cell Biol       Date:  1981       Impact factor: 1.441

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Authors:  E Holtzman
Journal:  Methods Cell Biol       Date:  1981       Impact factor: 1.441

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Authors:  C Oliver; A R Hand
Journal:  Methods Cell Biol       Date:  1981       Impact factor: 1.441

8.  Membrane flow during pinocytosis. A stereologic analysis.

Authors:  R M Steinman; S E Brodie; Z A Cohn
Journal:  J Cell Biol       Date:  1976-03       Impact factor: 10.539

9.  Microdomains of distinctive glycoprotein composition in the kidney proximal tubule brush border.

Authors:  D Kerjaschki; L Noronha-Blob; B Sacktor; M G Farquhar
Journal:  J Cell Biol       Date:  1984-04       Impact factor: 10.539

10.  Pinocytosis in mouse L-fibroblasts: ultrastructural evidence for a direct membrane shuttle between the plasma membrane and the lysosomal compartment.

Authors:  B Van Deurs; K Nilausen
Journal:  J Cell Biol       Date:  1982-08       Impact factor: 10.539

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