TY - JOUR
T1 - Optical dysfunction of the crystalline lens in aquaporin-0-deficient mice
AU - Shiels, Alan
AU - Bassnett, Steven
AU - Varadaraj, Kulandaiappa
AU - Mathias, Richard
AU - Al-Ghoul, Kristin
AU - Kuszak, Jer
AU - Donoviel, Dorit
AU - Lilleberg, Stan
AU - Friedrich, Glenn
AU - Zambrowicz, Brian
PY - 2002/1
Y1 - 2002/1
N2 - Aquaporin-0 (AQP0), a water transport channel protein, is the major intrinsic protein (MIP) of lens fiber cell plasma membranes. Mice deficient in the gene for AQP0 (Aqp0, Mip) were generated from a library of gene trap embryo stem cells. Sequence analysis showed that the gene trap vector had inserted into the first exon of Aqp0, causing a null mutation as verified by RNA blotting and immunochemistry. At 3 wk of age (postnatal day 21), lenses from null mice (Aqp0-/-) contained polymorphic opacities, whereas lenses from heterozygous mice (Aqp0+/-) were transparent and did not develop frank opacities until ∼24 wk of age. Osmotic water permeability values for Aqp0+/- and Aqp0-/- lenses were reduced to ∼46% and ∼20% of wild-type values, respectively, and the focusing power of Aqp0+/- lenses was significantly lower than that of wild type. These findings show that heterozygous loss of AQPO is sufficient to trigger cataractogenesis in mice and suggest that this MIP is required for optimal focusing of the crystalline lens.
AB - Aquaporin-0 (AQP0), a water transport channel protein, is the major intrinsic protein (MIP) of lens fiber cell plasma membranes. Mice deficient in the gene for AQP0 (Aqp0, Mip) were generated from a library of gene trap embryo stem cells. Sequence analysis showed that the gene trap vector had inserted into the first exon of Aqp0, causing a null mutation as verified by RNA blotting and immunochemistry. At 3 wk of age (postnatal day 21), lenses from null mice (Aqp0-/-) contained polymorphic opacities, whereas lenses from heterozygous mice (Aqp0+/-) were transparent and did not develop frank opacities until ∼24 wk of age. Osmotic water permeability values for Aqp0+/- and Aqp0-/- lenses were reduced to ∼46% and ∼20% of wild-type values, respectively, and the focusing power of Aqp0+/- lenses was significantly lower than that of wild type. These findings show that heterozygous loss of AQPO is sufficient to trigger cataractogenesis in mice and suggest that this MIP is required for optimal focusing of the crystalline lens.
KW - Cataract
KW - Gene trap
KW - Mouse
KW - Water channel
UR - http://www.scopus.com/inward/record.url?scp=19044392016&partnerID=8YFLogxK
M3 - Article
C2 - 11773604
AN - SCOPUS:19044392016
SN - 1531-2267
VL - 2002
SP - 179
EP - 186
JO - Physiological genomics
JF - Physiological genomics
IS - 7
ER -