Na+/H+ exchanger isoforms are differentially regulated in rat submandibular gland during acid/base disturbances in vivo
2006 | journal article. A publication with affiliation to the University of Göttingen.
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Na+/H+ exchanger isoforms are differentially regulated in rat submandibular gland during acid/base disturbances in vivo
Oehlke, O.; Sprysch, P.; Rickmann, M. & Roussa, E. (2006)
Cell and Tissue Research, 323(2) pp. 253-262. DOI: https://doi.org/10.1007/s00441-005-0055-6
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- Authors
- Oehlke, O.; Sprysch, P.; Rickmann, Michael; Roussa, Eleni
- Abstract
- Acute metabolic acidosis and alkalosis cause a series of homeostatic adaptive responses in the kidney and other epithelia. We hypothesized that acid/base disturbances might affect the expression of Na+/H+ stop exchanger (NHE) isoforms in salivary glands and determined the expression and cellular distribution of NHE3 and NHE4 in rat submandibular glands of controls and after imposed acute or chronic metabolic acidosis or alkalosis in vivo. Reverse transcription/polymerase chain reaction, in situ hybridization, and immunohistochemistry were applied by using specific primers, antisense probes, and antibodies, respectively. The results showed NHE3 and NHE4 transcript expression and protein abundance in rat submandibular gland. NHE3 was apically localized in duct cells, whereas NHE4 was found basolaterally distributed in acinar and duct cells. Acute acidosis and alkalosis and chronic acidosis had no effect on NHE3 and NHE4 expression and localization. In contrast, chronic metabolic alkalosis significantly decreased the number of apically stained NHE3 duct cells but had no effect on NHE3 mRNA expression. The results demonstrate, for the first time, the presence of NHE4 protein in salivary glands. The data also indicate the distinct regulation and adaptive changes of different isoforms of the same transporter in rat submandibular gland as a response to acid/base disturbances.
- Issue Date
- 2006
- Status
- published
- Publisher
- Springer
- Journal
- Cell and Tissue Research
- ISSN
- 0302-766X