Preparing your results

Our searching services are busy right now. Your search will reload in five seconds.

Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

NaBC1 (the SLC4A11 gene) belongs to the SLC4 family of sodium-coupled bicarbonate (carbonate) transporter proteins and functions as an electrogenic sodium borate cotransporter. Mutations in SLC4A11 cause either corneal abnormalities (corneal hereditary dystrophy type 2) or a combined auditory and visual impairment (Harboyan syndrome). The role of NaBC1 in sensory systems is poorly understood, given the difficulty of studying patients with NaBC1 mutations. We report our findings in Slc4a11(-/-) mice generated to investigate the role of NaBC1 in sensorineural systems. In wild-type mice, specific NaBC1 immunoreactivity was detected in fibrocytes of the spiral ligament, from the basal to the apical portion of the cochlea. NaBC1 immunoreactivity was present in the vestibular labyrinth, in stromal cells underneath the non-immunoreactive sensory epithelia of the macula utricle, sacule, and crista ampullaris, and the membranous vestibular labyrinth was collapsed. Both auditory brain response and vestibular evoked potential waveforms were significantly abnormal in Slc4a11(-/-) mice. In the cornea, NaBC1 was highly expressed in the endothelial cell layer with less staining in epithelial cells. However, unlike humans, the corneal phenotype was mild with a normal slit lamp evaluation. Corneal endothelial cells were morphologically normal; however, both the absolute height of the corneal basal epithelial cells and the relative basal epithelial cell/total corneal thickness were significantly increased in Slc4a11(-/-) mice. Our results demonstrate for the first time the importance of NaBC1 in the audio-vestibular system and provide support for the hypothesis that SLC4A11 should be considered a potential candidate gene in patients with isolated sensorineural vestibular hearing abnormalities.

Pubmed ID: 19586905 RIS Download

Mesh terms: Animals | Anion Transport Proteins | Antiporters | Audiometry, Evoked Response | Cochlea | Cornea | Epithelial Cells | Evoked Potentials, Auditory, Brain Stem | Female | Hearing Loss, Sensorineural | Humans | Immunoblotting | Immunohistochemistry | Immunoprecipitation | Male | Mice | Mice, Inbred C57BL | Mice, Knockout | Motor Activity | Symporters

Research resources used in this publication

None found

Research tools detected in this publication

None found

Data used in this publication

None found

Associated grants

  • Agency: NIDCD NIH HHS, Id: DC006443
  • Agency: NIDDK NIH HHS, Id: DK058563
  • Agency: NIDDK NIH HHS, Id: DK063125
  • Agency: NIDDK NIH HHS, Id: DK077162
  • Agency: NEI NIH HHS, Id: EY015829
  • Agency: NEI NIH HHS, Id: EY019561
  • Agency: NIDCD NIH HHS, Id: R01 DC006443
  • Agency: NIDCD NIH HHS, Id: R01 DC006443-04
  • Agency: Howard Hughes Medical Institute, Id:

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.