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Deletion of aquaporin‐4 renders retinal glial cells more susceptible to osmotic stress
Author(s) -
Pannicke Thomas,
Wurm Antje,
Iandiev Ianors,
Hollborn Margrit,
Linnertz Regina,
Binder Devin K.,
Kohen Leon,
Wiedemann Peter,
Steinhäuser Christian,
Reichenbach Andreas,
Bringmann Andreas
Publication year - 2010
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.22437
Subject(s) - aquaporin 4 , retinal , retina , microbiology and biotechnology , osmotic shock , astrocyte , neuroglia , endocrinology , chemistry , muller glia , medicine , biology , neuroscience , biochemistry , central nervous system , stem cell , progenitor cell , gene
The glial water channel aquaporin‐4 (AQP4) is implicated in the control of ion and osmohomeostasis in the sensory retina. Using retinal slices from AQP4‐deficient and wild‐type mice, we investigated whether AQP4 is involved in the regulation of glial cell volume under altered osmotic conditions. Superfusion of retinal slices with a hypoosmolar solution induced a rapid swelling of glial somata in tissues from AQP4 null mice but not from wild‐type mice. The swelling was mediated by oxidative stress, inflammatory lipid mediators, and sodium influx into the cells and was prevented by activation of glutamatergic and purinergic receptors. Distinct inflammatory proteins, including interleukin‐1β, interleukin‐6, and inducible nitric oxide synthase, were up‐regulated in the retina of AQP4 null mice compared with control, whereas cyclooxygenase‐2 was down‐regulated. The data suggest that water flux through AQP4 is involved in the rapid volume regulation of retinal glial (Müller) cells in response to osmotic stress and that deletion of AQP4 results in an inflammatory response of the retinal tissue. Possible implications of the data for understanding the pathophysiology of neuromyelitis optica, a human disease that has been suggested to involve serum antibodies to AQP4, are discussed. © 2010 Wiley‐Liss, Inc.