Distribution of type IV collagen in the cochlea in Alport syndrome

Archives of Otolaryngology - Head and Neck Surgery

Volumn 131, Issue 11, 2005, Pages 1007-1013

  Zehnder, Andreas F ^a,b   Adams, Joe C ^b,c   Santi, Peter A ^e   Kristiansen, Arthur G ^b   Wacharasindhu, Chitsuda ^b   Mann, Sabine ^b   Kalluri, Raghu ^d   Gregory, Martin C ^g   Kashtan, Clifford E ^f   Merchant, Saumil N ^b,c  

^a UNIVERSITY HOSPITAL BASEL   (Switzerland)

^b MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

^d BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

^e UNIVERSITY OF MINNESOTA   (United States)

^f UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^g UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 4;

ADULT; ALPHA CHAIN; ALPORT SYNDROME; ARTICLE; BASEMENT MEMBRANE; BLOOD VESSEL; CASE REPORT; COCHLEA; CONTROLLED STUDY; EAR; FEMALE; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; LIGAMENT; MALE; PERCEPTION DEAFNESS; PROTEIN LOCALIZATION; SCHWANN CELL; TISSUE DISTRIBUTION;

ADULT; BASEMENT MEMBRANE; CASE-CONTROL STUDIES; COCHLEA; COLLAGEN TYPE IV; COLORING AGENTS; EOSINE YELLOWISH-(YS); FEMALE; FLUORESCENT DYES; HEARING LOSS, SENSORINEURAL; HEMATOXYLIN; HUMANS; MALE; MICROSCOPY, POLARIZATION; MIDDLE AGED; MUTATION; NEPHRITIS, HEREDITARY; SCHWANN CELLS;

EID: 28144465642     PISSN: 08864470     EISSN: 08864470     Source Type: Journal    
DOI: 10.1001/archotol.131.11.1007     Document Type: Article

References (23)

1. Alport AC. Hereditary familial congenital haemorrhagic nephritis. BMJ. 1927;1:504-506.
2. Kashtan CE. Alport syndrome: an inherited disorder of renal, ocular and cochlear basement membranes. Medicine (Baltimore). 1999;78:338-360.
3. Hudson BG, Tryggvason K, Sundaramoorthy M, Neilson EG. Alport syndrome, Goodpasture's syndrome, and type IV collagen. N Engl J Med. 2003;348:2543-2556.
4. Kalluri R, Cosgrove D. Assembly of type IV collagen: insights from α3(IV) collagen-deficient mice. J Biol Chem. 2000;275:12719-12724.
5. Miner JH, Sanes JR. Collagen IV a3, a4 and a5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches. J Cell Biol. 1994;127:879-891.
6. Kalluri R, Shield CF, Todd P, Hudson BG, Neilson EG. Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis. J Clin Invest. 1997;99:2470-2478.
7. Harvey SJ, Zheng K, Sado Y, et al. Role of distinct type IV collagen networks in glomerular development and function. Kidney Int. 1998;54:1857-1866.
8. Merchant SN, Burgess BJ, Adams JC, et al. Temporal bone histopathology in Alport syndrome. Laryngoscope. 2004;114:1609-1618.
9. Kleppel MM, Santi PA, Cameron JD, Wieslander J, Michael AF. Human tissue distribution of novel basement membrane collagen. Am J Pathol. 1989;134:813-825.
10. Adams JC. Biotin amplification of biotin and horseradish peroxidase signals in histochemical stains. J Histochem Cytochem. 1992;40:1457-1463.
11. Cosgrove D, Kornak JM, Samuelson G. Expression of basement membrane type IV collagen chains during postnatal development in the murine cochlea. Hear Res. 1996;100:21-32.
12. Cosgrove D, Samuleson G, Meehan DT, et al. Ultrastructural, physiological, and molecular defects in the inner ear of a gene-knockout mouse model for autosomal Alport syndrome. Hear Res. 1998;121:84-98.
13. Fujita S, Hayden RC. Alport's syndrome: temporal bone report. Arch Otolaryngol. 1969;90:453-466.
14. Myers GJ, Tyler HR. The etiology of deafness in Alport's syndrome. Arch Otolaryngol. 1972;96:333-340.
15. Smith RJH, Steel KP, Barkway C, Soucek S, Michaels L. A histologic study of nonmorphogenetic forms of hereditary hearing impairment. Arch Otolaryngol Head Neck Surg. 1992;118:1085-1094.
16. Schuknecht HF. Pathology of the Ear. 2nd ed. Philadelphia, Pa: Lea and Febiger; 1993.
17. Rintelmann W. Auditory manifestations of Alport's disease syndrome. Trans Sect Otolaryngol Am Acad Ophthalmol Otolaryngol. 1976;82:375-387.
18. Gleeson MJ. Alport's syndrome: audiological manifestations and implications. J Laryngol Otol. 1984;98:449-465.
19. Weber PC, Cunningham CD III, Schulte BA. Potassium recycling pathways in the human cochlea. Laryngoscope. 2001;111:1156-1165.
20. Adams JC. Clinical implications of inflammatory cytokines in the cochlea: a technical note. Otol Neurotol. 2002;23:316-322.
21. Shen Z, Liang F, Hazen-Martin DJ, Schulte BA. BK channels mediate the voltage-dependent outward current in type I spiral ligament fibrocytes. Hear Res. 2004;187:35-43.
22. Harvey SJ, Mount R, Sado Y, et al. The inner ear of dogs with X-linked nephritis provides clues to the pathogenesis of hearing loss in X-linked Alport syndrome. Am J Pathol. 2001;159:1097-1104.
23. Kashtan CE. Animal models of Alport syndrome (editorial comments). Nephrol Dial Transplant. 2002;17:1359-1361.