Compartmentation of multiple forms of creatine kinase in the distal nephron of the rat kidney
Creatine kinase enzymes are present in tissues such as muscle and brain to interconvert creatine phosphate and ADP, thus providing a system to interconnect energy production and utilization (Bessman, S. P., and Carpenter, C. L. (1985) Annu. Rev. Biochem. 54, 831-862). Creatine kinase isoenzymes in k...
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Veröffentlicht in: | The Journal of biological chemistry 1991-11, Vol.266 (33), p.22404-22410 |
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Zusammenfassung: | Creatine kinase enzymes are present in tissues such as muscle and brain to interconvert creatine phosphate and ADP, thus providing
a system to interconnect energy production and utilization (Bessman, S. P., and Carpenter, C. L. (1985) Annu. Rev. Biochem.
54, 831-862). Creatine kinase isoenzymes in kidney have received little attention since kidney contains relatively low creatine
kinase activity compared with muscle and brain and because there is disagreement regarding the identity of the specific isoforms
expressed in kidney. Using a combination of chromatographic and immunological techniques, we have identified two isoforms
of creatine kinase in rat kidney supernatants, B creatine kinase, and the non-sarcomeric form of the mitochondrial creatine
kinase, which represent 82 and 15%, respectively, of the total creatine kinase activity in this tissue. The identity of the
non-muscle form of the mitochondrial creatine kinase was confirmed by N-terminal sequence analysis and compared with recently
published cDNA sequences (Haas, R. C., and Strauss, A. W. (1990) J. Biol. Chem. 265, 6921-6927). We prepared multiple antisera
specific for each isoform using synthetic peptide immunogens based upon nonhomologous regions from the primary sequence of
each creatine kinase isoform. Immunocytochemical results demonstrate that both creatine kinase isoforms are colocalized in
the inner stripe of the outer medulla in tubules of the distal nephron. A similar distribution of creatine kinase isoforms
was obtained when different layers of the renal cortex and medulla were examined for creatine kinase activity and isozyme
content using nondenaturing electrophoresis. In general, the distribution of creatine kinase enzymes in kidney corresponds
to the regions of greatest ATP utilization, oxygen consumption, and sodium transport. These results suggest a role for creatine
kinase enzymes in the coupling of ion transport and oxidative phosphorylation in the distal nephron of the mammalian kidney. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1016/s0021-9258(18)54587-7 |