Distribution of type IV collagen in the cochlea in Alport syndrome

Andreas F. Zehnder, Joe C. Adams, Peter A. Santi, Arthur G. Kristiansen, Chitsuda Wacharasindhu, Sabine Mann, Raghu Kalluri, Martin C. Gregory, Clifford E. Kashtan, Saumil N. Merchant

Research output: Contribution to journalArticlepeer-review

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Objective: To determine the distribution of α1, α3, and α5 chains of type IV collagen in the cochlea in Alport syndrome. Design: Case-control study. Patients: Two patients with sensorineural hearing loss due to Alport syndrome. Both patients had known mutations in the COL4A5 gene. Main Outcome Measures: Immunostaining was used to study the distribution of type IV collagen (α1, α3, and α5 chains) within the cochlea. Immunostaining was also performed in the cochlear tissues of an unaffected individual used as a control. Results: In the control ear, α1 staining was observed in the basement membrane overlying the basilar membrane, in the basement membrane of cochlear blood vessels and Schwann cells, and within the spiral limbus. In the control ear, we also observed strong staining for α3 and α5 chains in the basement membrane overlying the basilar membrane and within the spiral ligament. In both cases with Alport syndrome, no immunostaining was observed for α3 or α5 chains within the cochlea, whereas α1 staining was present in locations similar to that seen in the control ear. Conclusions: The results indicate that isotype switching does not occur within the cochlea in Alport syndrome. The results are also consistent with the hypothesis that the sensorineural hearing loss in Alport syndrome may be due to alterations in cochlear micromechanics and/or dysfunction of the spiral ligament.

Original languageEnglish (US)
Pages (from-to)1007-1013
Number of pages7
JournalArchives of Otolaryngology - Head and Neck Surgery
Issue number11
StatePublished - Nov 2005


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