HEMOGLOBIN ABSORPTION BY THE CELLS OF THE PROXIMAL CONVOLUTED TUBULE IN MOUSE KIDNEY
Open Access
- 1 December 1960
- journal article
- research article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 8 (3) , 689-718
- https://doi.org/10.1083/jcb.8.3.689
Abstract
The formation of protein absorption droplets in the cells of the proximal convolution was studied in mouse kidney. Ox hemoglobin was administered intraperitoneally and kidney specimens were collected at intervals of 30 minutes to 4 days after injection. In the lumen of the nephron, hemoglobin was concentrated to an opaque mass whose relations with the brush border and the epithelium could be easily followed. It was found that hemoglobin passes through the brush border in between the microvilli, enters the channels of tubular invaginations at the bases of the brush border, and is transported in bulk into vacuoles in the intermediate cell zone. These vacuoles increase in size and are transformed through further concentration into dense absorption droplets. Using the opaque hemoglobin content of the nephron as a tracer, functional continuity of the system of the tubular invaginations with the lumen on one side and the vacuoles on the other was demonstrated. Mitochondria lie closely apposed to vacuoles and droplets, but are not primarily involved in droplet formation. 15 hours after injection and later, ferritin and systems of layered membranes become visible in the droplets as their density decreases. These membranes are interpreted as lipoprotein membranes; similar membranes are found in the lumen of the tubuli. It is suggested that phospholipids enter into the vacuoles together with hemoglobin from the tubular lumen and form membrane systems of lipoproteins in the droplets. At 3 to 4 days the droplets contain aggregates of ferritin, and the iron reaction becomes positive in the tubule cells. No significant changes were found in the Golgi apparatus or in the microbodies during hemoglobin absorption. At all time points investigated, the terminal bars seal the intercellular spaces against penetration by hemoglobin in the proximal and distal convolutions and in the collecting ducts.Keywords
This publication has 49 references indexed in Scilit:
- Segregation of Ferritin in Glomerular Protein Absorption DropletsThe Journal of cell biology, 1960
- Changes in the Fine Structure of Rat Liver Cells Brought about by DimethylnitrosamineThe Journal of cell biology, 1960
- An Electron Microscope Study of the Salamander Thyroid during Hormonal StimulationThe Journal of cell biology, 1960
- Staining of Tissue Sections for Electron Microscopy with Heavy MetalsThe Journal of cell biology, 1958
- REDUCTION OF HEATING ARTIFACTS IN THIN SECTIONS EXAMINED IN THE ELECTRON MICROSCOPEThe Journal of cell biology, 1957
- CELLULAR MECHANISMS OF PROTEIN METABOLISM IN THE NEPHRONThe Journal of Experimental Medicine, 1955
- FINE STRUCTURES OF THE KIDNEY SEEN BY ELECTRON MICROSCOPYJournal of Histochemistry & Cytochemistry, 1955
- CELLULAR MECHANISMS OF PROTEIN METABOLISM IN THE NEPHRONThe Journal of Experimental Medicine, 1954
- CELLULAR MECHANISMS OF PROTEIN METABOLISM IN THE NEPHRONThe Journal of Experimental Medicine, 1954
- CELLULAR MECHANISMS OF PROTEIN METABOLISM IN THE NEPHRONThe Journal of Experimental Medicine, 1954