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cotransporter expression in rat skeletal muscle
Department of Physiology, College of Medicine, University of Tennessee, Memphis 38163
Doubt has been raised about the expression
of a functional
Na+-K+-2Cl
cotransporter in rat skeletal muscle. In this study we present molecular and functional evidence for expression of a protein having
the characteristics of a cotransporter. RT-PCR of RNA isolated from rat
soleus muscle with primers to a conserved putative membrane-spanning domain resulted in a single product of predicted size. Sequencing of
the product showed that it bears >90% homology with known rodent NKCC1 (BSC2) cotransporters. RNase protection assay of RNA isolated from the rat soleus muscle also identified this sequence. Immunologic detection of the cotransporter with two different antibodies indicated the presence of cotransporter protein, perhaps more than one, in blots
of total muscle protein. Immunohistochemical detection by confocal
microscopy localized the majority of expression of the protein to the
muscle fibers. Functional studies of cotransport activity also indicate
the appropriate sensitivity to inhibitors and ion dependence. Taken
together, these data support the presence and function of
Na+-K+-2Cl
cotransporter activity in the soleus muscle of the rat.
Na+-K+-2Cl
cotransporter; bumetanide-sensitive cotransporter 2; NKCC1; ion
transport; soleus muscle
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