Apical endosomes isolated from kidney collecting duct principal cells lack subunits of the proton pumping ATPase.
Open Access
- 1 October 1992
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 119 (1) , 111-122
- https://doi.org/10.1083/jcb.119.1.111
Abstract
Endocytic vesicles that are involved in the vasopressin-stimulated recycling of water channels to and from the apical membrane of kidney collecting duct principal cells were isolated from rat renal papilla by differential and Percoll density gradient centrifugation. Fluorescence quenching measurements showed that the isolated vesicles maintained a high, HgCl2-sensitive water permeability, consistent with the presence of vasopressin-sensitive water channels. They did not, however, exhibit ATP-dependent luminal acidification, nor any N-ethylmaleimide-sensitive ATPase activity, properties that are characteristic of most acidic endosomal compartments. Western blotting with specific antibodies showed that the 31- and 70-kD cytoplasmically oriented subunits of the vacuolar proton pump were not detectable in these apical endosomes from the papilla, whereas they were present in endosomes prepared in parallel from the cortex. In contrast, the 56-kD subunit of the proton pump was abundant in papillary endosomes, and was localized at the apical pole of principal cells by immunocytochemistry. Finally, an antibody that recognizes the 16-kD transmembrane subunit of oat tonoplast ATPase cross-reacted with a distinct 16-kD band in cortical endosomes, but no 16-kD band was detectable in endosomes from the papilla. This antibody also recognized a 16-kD band in affinity-purified H+ ATPase preparations from bovine kidney medulla. Therefore, early endosomes derived from the apical plasma membrane of collecting duct principal cells fail to acidify because they lack functionally important subunits of a vacuolar-type proton pumping ATPase, including the 16-kD transmembrane domain that serves as the proton-conducting channel, and the 70-kD cytoplasmic subunit that contains the ATPase catalytic site. This specialized, non-acidic early endosomal compartment appears to be involved primarily in the hormonally induced recycling of water channels to and from the apical plasma membrane of vasopressin-sensitive cells in the kidney collecting duct.Keywords
This publication has 54 references indexed in Scilit:
- The role of membrane turnover in the water permeability response to antidiuretic hormoneThe Journal of Membrane Biology, 1988
- Apical membrane endocytosis via coated pits is stimulated by removal of antidiuretic hormone from isolated, perfused rabbit cortical collecting tubuleThe Journal of Membrane Biology, 1988
- Endosomes from kidney collecting tubule cells contain the vasopressin-sensitive water channelNature, 1988
- Proton translocating ATPases: Issues in structure and functionKidney International, 1988
- [11] Coupled assay of Na+,K+-ATPase activityPublished by Elsevier ,1988
- Structure of the novel membrane-coating material in proton-secreting epithelial cells and identification as an H+ATPase.The Journal of cell biology, 1987
- Apical membrane area of rabbit urinary bladder increases by fusion of intracellular vesicles: An electrophysiological studyThe Journal of Membrane Biology, 1984
- Vasopressin stimulates formation of coated pits in rat kidney collecting ductsNature, 1983
- Fluorescence Microscopy: Reduced Photobleaching of Rhodamine and Fluorescein Protein Conjugates by n -Propyl GallateScience, 1982
- A high yield preparation for rat kidney brush border membranes Different behaviour of lysosomal markersBiochimica et Biophysica Acta (BBA) - Biomembranes, 1981