Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing loss
- Author(s)
- Guipponi, M; Tan, J; Cannon, PZF; Donley, L; Crewther, P; Clarke, M; Wu, QY; Shepherd, RK; Scott, HS;
- Details
- Publication Year 2007-08,Volume 171,Issue #2,Page 608-616
- Journal Title
- AMERICAN JOURNAL OF PATHOLOGY
- Publication Type
- Journal Article
- Abstract
- Defective proteolysis has been implicated in hearing loss through the discovery of mutations causing autosomal recessive nonsyndromic deafness in a type II transmembrane serine protease gene, TMPRSS3. To investigate their physiological function and the contribution of this family of proteases to the auditory function, we analyzed the hearing status of mice deficient for hepsin, also known as TMPRSS1. These mice exhibited profound hearing loss with elevated hearing thresholds compared with their heterozygous and wild-type littermates. Their cochleae showed abnormal tectorial membrane development, reduction in fiber compaction in the peripheral portion of the auditory nerve, and decreased expression of the myelin proteins myelin basic protein and myelin protein zero. In addition, reduced level of the large conductance voltage- and Ca (2+)-activated K+ channel was detected in the sensory hair cells of T'mprss1-null mice. We examined thyroid hormone levels in Tmprss1-deficient mice, as similar cochlear defects have been reported in animal models of hypothyroidism, and found significantly reduced free thyroxine levels. These data show that TMPRSS1 is required for normal auditory function. Hearing impairment present in Tmprss1-null mice is characterized by a combination of various structural, cellular, and molecular abnormalities that are likely to affect different cochlear processes.
- Publisher
- AMER SOC INVESTIGATIVE PATHOLOGY, INC
- Keywords
- AUTOSOMAL RECESSIVE DEAFNESS; HORMONE RECEPTOR-BETA; MYOSIN-VIIA GENE; THYROID-HORMONE; NONSYNDROMIC DEAFNESS; MUTATIONS; TMPRSS3; COCHLEA; EXPRESSION; MOUSE
- Publisher's Version
- https://doi.org/10.2353/ajpath.2007.070068
- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2007-08-01 12:00:00