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Am J Physiol Renal Physiol 284: F358-F364, 2003. First published October 29, 2002; doi:10.1152/ajprenal.00100.2002
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Vol. 284, Issue 2, F358-F364, February 2003

Dissociation of spectrin-ankyrin complex as a basis for loss of Na-K-ATPase polarity after ischemia

Robert Woroniecki1, Jean R. Ferdinand1, Jon S. Morrow2, and Prasad Devarajan1,3

1 Division of Pediatric Nephrology, Albert Einstein College of Medicine, New York, New York 10467; 2 Division of Pathology, Yale University School of Medicine, New Haven, Connecticut 06520; and 3 Department of Nephrology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229-3039

The polarized distribution of Na-K-ATPase at the basolateral membranes of renal tubule epithelial cells is maintained via a tethering interaction with the underlying spectrin-ankyrin cytoskeleton. In this study, we have explored the mechanism underlying the loss of Na-K-ATPase polarity after ischemic injury in Madin-Darby canine kidney (MDCK) cells, utilizing a novel antibody raised against a recently described kidney-specific isoform of ankyrin. In control MDCK cells, ankyrin was colocalized with Na-K-ATPase at the basolateral membrane. ATP depletion resulted in a duration-dependent mislocation of Na-K-ATPase and ankyrin throughout the cytoplasm. Colocalization studies showed a partial overlap between the distribution of ankyrin and Na-K-ATPase at all periods after ATP depletion. By immunoprecipitation with anti-ankyrin antibody, the mislocated Na-K-ATPase remained bound to ankyrin at all time points after ATP depletion. However, the interaction between ankyrin and spectrin was markedly diminished within 3 h of ATP depletion and was completely lost after 6 h. In solution binding assays using a fusion peptide of glutathione S-transferase with the ankyrin binding domain of Na-K-ATPase, a complex with ankyrin was detected at all time points after ATP depletion, but spectrin was lost from the complex in a duration-dependent manner. The loss of spectrin binding was not attributable to spectrin degradation but was associated with hyperphosphorylation of ankyrin. The results suggest that a dissociation of the membrane-cytoskeleton complex at the spectrin-ankyrin interface may contribute to the loss of Na-K-ATPase polarity after ischemic injury and reaffirm a critical adapter role for ankyrin in the normal maintenance of Na-K-ATPase polarity.

phosphorylation; Madin-Darby canine kidney; adenosine 5'-triphosphatase depletion


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