1. Subcellular fractions of rat kidney cortex generated angiotensin I continuously over 2h when incubated at 37degreesC with rat renin, indicating the presence of renin substrate within cells in the renal cortex. 2. Renin substrate was located in highest specific concentration in particulate fractions. The particles containing renin substrate had a sedimentation velocity slightly lower than mitochondria and renin granules but greater than the microsomal fraction. 3. Isopycnic gradient centrifugation indicated a density of 1.190g/ml for the particles containing renin substrate, compared with 1.201 for renin granules, 1.177 for mitochondria, and 1.170 and 1.230 for lysosomes in the heavy-granule fraction. 4. In the liver, renin substrate was also found in particles, but these had a lower sedimentation rate than those from the kidney. 5. The molecular weights of renin substrate in kidney and liver granules and rat plasma were similar, namely 61000-62000. 6. On the basis of these biochemical findings, a mechanism for the intrarenal production of angiotensin, incorporating a subcellular reaction scheme, is proposed.
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March 1976
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Research Article|
March 15 1976
Renin substrate in granules from rat kidney cortex
B J. Morris;
B J. Morris
1Monash University Department of Medicine, Prince Henry's Hospital, St. Kilda Road, Melbourne, Vic. 3004, Australia
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C I. Johnston
C I. Johnston
1Monash University Department of Medicine, Prince Henry's Hospital, St. Kilda Road, Melbourne, Vic. 3004, Australia
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Publisher: Portland Press Ltd
Online ISSN: 1470-8728
Print ISSN: 0264-6021
© 1976 London: The Biochemical Society
1976
Biochem J (1976) 154 (3): 625–637.
Citation
B J. Morris, C I. Johnston; Renin substrate in granules from rat kidney cortex. Biochem J 15 March 1976; 154 (3): 625–637. doi: https://doi.org/10.1042/bj1540625
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