Astrocyte-Specific Expression of Aquaporin-9 in Mouse Brain is Increased after Transient Focal Cerebral Ischemia

Journal of Cerebral Blood Flow and Metabolism - Tập 21 Số 5 - Trang 477-482 - 2001
Jérôme Badaut1,2, Lorenz Hirt3, Cristina Granziera3, Julien Bogousslavsky3, Pierre J. Magistretti3,2, Luca Regli1
1Department of Neurosurgery, Centre Hospitalier Universitaire Vaudois, Switzerland
2Institute of Physiology, University of Lausanne, 1011 Lausanne, Switzerland
3Department of Neurology, Centre Hospitalier Universitaire Vaudois, Switzerland

Tóm tắt

Aquaporin-9 (AQP9) is a new member of the aquaporin family of water-selective channels mainly expressed in liver and testis, presenting the characteristic of also being permeable to various solutes, particularly lactate. Recent data have shown the presence of AQP9 on tanycytes in the rat brain. In the current study, the authors show the expression of AQP9 in astrocytes in the mouse brain and changes in its expression after cerebral ischemia. Indeed, in control mouse, the AQP9 immunolabeling is present on astrocytic processes bordering the subarachnoid space and ventricles. The labeling also is observed on astrocytes in the white matter, hippocampus, hypothalamus, and lateral septum. After focal transient ischemia, an increase of the immunolabeling is detected on astrocytes in periinfarct areas. This AQP9 distribution study in mouse brain suggests a role of AQP9 in water homeostasis in the central nervous system. Furthermore, the overexpression of AQP9 on astrocytes surrounding an ischemic lesion suggests that AQP9 may also play a role in the regulation of postischemia edema and, in view of its permeability to monocarboxylates, in the clearance of lactate from the ischemic focus.

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Tài liệu tham khảo

10.1016/0306-4522(94)90372-7

10.1046/j.1365-2826.2000.00539.x

10.1016/S0304-3940(00)01364-1

10.1146/annurev.physiol.59.1.601

10.1007/BF00238100

10.1006/bbrc.2000.3505

10.1126/science.7522345

10.1006/bbrc.1998.8252

Klatzo I, 1994, Acta Neurochir Suppl (Wien), 60, 3

Ko SB, 1999, Biochem Mol Biol Int, 47, 309

10.1038/72256

10.1523/JNEUROSCI.17-01-00171.1997

10.1038/jcbfm.1990.47

10.1016/S0169-328X(00)00084-X

10.1074/jbc.273.38.24737

10.1016/S0301-0082(00)00035-6

10.1006/nbdi.1999.0246

10.1046/j.1460-9568.1999.00502.x