Tissue Distribution and Membrane Localization of Aquaporin-9 Water Channel
- 1 December 2001
- journal article
- Published by SAGE Publications in Journal of Histochemistry & Cytochemistry
- Vol. 49 (12) , 1547-1556
- https://doi.org/10.1177/002215540104901208
Abstract
Aquaporin-9 (AQP9) is a water channel membrane protein also permeable to small solutes such as urea, glycerol, and 5-fluorouracil, a chemotherapeutic agent. With the aim of understanding the pathophysiological role of AQP9, we performed an extensive analysis by Western blotting, RT-PCR, and immunolocalization in rat tissues. Western blotting analysis revealed a major band of approximately 32 kD in testis, liver, and brain. Immunofluorescence showed strong expression of AQP9 in the plasma membrane of testis Leydig cells. In liver, AQP9 expression was found to be sex-linked. Male rats had higher levels of AQP9 than female in terms of both protein and mRNA. Moreover, in female livers the expression of AQP9 was mostly confined to perivascular hepatocytes, whereas males showed a more homogeneous hepatocyte staining. No differences in AQP9 expression level related to the age or to protein content of the diet were found, indicating that differences in the liver may be gender-dependent. In the brain, AQP9 expression was found in tanycytes mainly localized in the areas lacking a blood-brain barrier (BBB), such as the circumventricular organs (CVOs) of the third ventricles, the subfornical organ, the hypothalamic regions, and the glial processes of the pineal gland. AQP9 expression in the osmosensitive region of the brain suggests a role in the mechanism of central osmoreception. All these findings show a unique tissue distribution of AQP9 compared to the other known aquaporins.Keywords
This publication has 18 references indexed in Scilit:
- The Water Channel Aquaporin-8 Is Mainly Intracellular in Rat Hepatocytes, and Its Plasma Membrane Insertion Is Stimulated by Cyclic AMPJournal of Biological Chemistry, 2001
- Muscle loading modulates aquaporin‐4 expression in skeletal muscleThe FASEB Journal, 2001
- Aquaporin‐4 deficiency in skeletal muscle and brain of dystrophic mdx miceThe FASEB Journal, 2000
- Immunolocalization of AQP9 in Liver, Epididymis, Testis, Spleen, and BrainBiochemical and Biophysical Research Communications, 2000
- Expression of aquaporin-4 in fast-twitch fibers of mammalian skeletal muscle.Journal of Clinical Investigation, 1998
- Cloning and Functional Expression of a New Aquaporin (AQP9) Abundantly Expressed in the Peripheral Leukocytes Permeable to Water and Urea, but Not to GlycerolBiochemical and Biophysical Research Communications, 1998
- Rat Hepatocytes Transport Water Mainly via a Non-channel-mediated PathwayJournal of Biological Chemistry, 1996
- Leydig Cells: Endocrine, Paracrine, and Autocrine RegulationEndocrine Reviews, 1994
- Endocrine Regulation and Communicating Functions of the Leydig CellAnnual Review of Physiology, 1988
- Cerebrospinal fluid-contacting area in the pineal recess of the vole (Microtus agrestis), Guinea Pig (Cavia cobaya), and rhesus monkey (Macaca mulatta)Cell and tissue research, 1980