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1 University of Bristol
2 University College London
3 Cambridge Institute for Medical Research
* To whom correspondence should be addressed. E-mail: ash.m.toye{at}bristol.ac.uk.
Rhesus glycoprotein homologs, RhAG, RhBG and RhCG, comprise a recently identified branch of the Mep/Amt ammonia transporter family. Animal studies have shown that RhBG and RhCG are present in the kidney distal tubules. Studies on mouse and rat tissue suggest a basolateral localization for RhBG in cells of the distal tubules including the
-intercalated cells (
-IC), but no localization of RhBG has been reported in human tissue. To date RhCG localization has been described as exclusively apical plasma membrane in mouse and rat kidney, or apical and basolateral in human, and some mouse and rat tissue studies. We raised novel antibodies to RhBG and RhCG to examine their localization in the human kidney. MDCKI cell lines stably expressing human GFP tagged RhBG or RhCG and human tissue lysates were used to demonstrate the specificity of these antibodies for detecting RhBG and RhCG. Using immunoperoxidase staining and antigen liberation techniques, both apical and basolateral RhCG localization was observed in the majority of the cells of the distal convoluted tubule and intercalated cells of the connecting tubule and collecting duct. Confocal microscopy imaging of normal human kidney cryosections showed that RhCG staining was predominantly localized to the apical membrane in these cells with some basolateral and intracellular staining evident. A proportion of RhCG staining labelled kAE1 positive cells, confirming that RhCG is localized to the
-IC cells. Surprisingly, no RhBG protein was detectable in human kidney by western blot analysis of tissue lysates using immunohistochemistry or confocal microscopy of tissue sections. The same antibodies however could detect RhBG in rat tissue. We conclude that under normal conditions RhCG is the major putative ammonia transporter expressed in human kidney and RhBG is not expressed at detectable levels.
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