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Cellular and subcellular distribution of exogenously administered renal renin in rat liver and kidney

Journal Article · · American Journal of Physiology; (USA)
OSTI ID:7025843
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  1. Osaka City Univ. Medical School (Japan) Kagawa Medical School (Japan) Tokyo Medical and Dental Univ. (Japan)

Using highly purified {sup 125}I-labeled rat renal renin, the authors have demonstrated that both the liver and kidney are responsible for clearance of renal renin. In the present study, light and electron microscope autoradiography of intravenously administered {sup 125}I-labeled rat renal renin was performed in rat liver and kidney to observe the cellular and subcellular distribution of the renin. Autoradiography was performed. In the liver, silver grains were mainly localized in Kupffer cells and not in hepatocytes. In the kidney, silver grains were evident in the proximal tubule cells. In both liver and kidney cells, silver grains were mainly located over the lysosomes. Gel permeation high-performance liquid chromatography analysis of the liver and kidney extracts indicated two main fractions, including immunoreactive {sup 125}I-renin and the breakdown products (free {sup 125}I and {sup 125}I-tyrosine). In conclusion, circulating renal renin is mainly taken up by Kupffer cells and proximal tubule cells and is subsequently transported to the lysosomes to be degraded. These results, taken together with the previous finding that nonglycosylated submaxillary renin does not distribute in the liver, suggest that the carbohydrate moieties of renal renin are necessary for the recognition by Kupffer cells.

OSTI ID:
7025843
Journal Information:
American Journal of Physiology; (USA), Journal Name: American Journal of Physiology; (USA) Vol. 253:6; ISSN 0002-9513; ISSN AJPHA
Country of Publication:
United States
Language:
English