[Ultrastructural localization of aquaporin 1 in endolymphatic sac of the mouse].

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi

Department of Otorhinolaryngology Head and Neck Surgery, Institute of Otorhinolaryngology, General Hospital of Chinese People's Liberation Army, Beijing 100853, China.

Published: March 2007

Objective: To study the ultrastructural localization of aquaporin 1 (AQP1) in the endolymphatic sac (ES) of the mouse inner ear and explore the function of the AQP1 in ES.

Methods: The cellular localization of AQP1 in ES of the mouse inner ear was investigated by immunocytochemistry. The ultrastructural localization of AQP1 in the mouse inner ear was performed by immunogold electron microscopy which is characterized as cryoprotection and high sensitivity.

Results: In the ES, strong AQP1 labeling was observed in the sub-epithelial connective tissue. Fibroblasts of sub-epithelial connective tissue of the ES present densely labeling of gold particles. But the epithelial cells of the ES were devoid of labeling. AQP1 was localized on the cell processes of the fibrocytes.

Conclusions: AQP1 in the ES may play an important role in absorbing water and regulate the balance of fluid and ion in the inner ear.

Download full-text PDF

Source

Publication Analysis

Top Keywords

inner ear
16
mouse inner
12
localization aquaporin
8
endolymphatic sac
8
ultrastructural localization
8
localization aqp1
8
aqp1 mouse
8
sub-epithelial connective
8
connective tissue
8
aqp1
7

Similar Publications

Foxm1 promotes differentiation of neural progenitors in the zebrafish inner ear.

Dev Biol

January 2025

Biology Department, Texas A&M University, College Station, TX 7843-3258. Electronic address:

During development of the vertebrate inner ear, sensory epithelia and neurons of the statoacoustic ganglion (SAG) arise from lineage-restricted progenitors that proliferate extensively before differentiating into mature post-mitotic cell types. Development of progenitors is regulated by Fgf, Wnt and Notch signaling, but how these pathways are coordinated to achieve an optimal balance of proliferation and differentiation is not well understood. Here we investigate the role in zebrafish of Foxm1, a transcription factor commonly associated with proliferation in developing tissues and tumors.

View Article and Find Full Text PDF

Non-syndromic hearing loss (NSHL) is a genetically heterogeneous disorder accounting for almost 70% of the total congenital hearing loss. The implementation of rapid advanced sequencing methods has significantly contributed to the correct molecular diagnosis for several rare genetic disorders, including NHSL. Features of two probands with NHSL were clinically and genetically evaluated.

View Article and Find Full Text PDF

Corrigendum: Characterization of expression in mouse cochlear hair cells.

Front Genet

December 2024

State Key Laboratory of Bioelectronics, School of Life Sciences and Technology, Jiangsu Province High-Tech Key Laboratory for Bio-Medical Research, Southeast University, Nanjing, China.

[This corrects the article DOI: 10.3389/fgene.2021.

View Article and Find Full Text PDF

Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity search.

Hum Genet

January 2025

Division of Hearing and Balance Research, National Institute of Sensory Organs, NHO Tokyo Medical Center, 2-5-1 Higashigaoka, Meguro-Ku, Tokyo, 152-8902, Japan.

There are hundreds of rare syndromic diseases involving hearing loss, many of which are not targeted for clinical genetic testing. We systematically explored the genetic causes of undiagnosed syndromic hearing loss using a combination of whole exome sequencing (WES) and a phenotype similarity search system called PubCaseFinder. Fifty-five families with syndromic hearing loss of unknown cause were analyzed using WES after prescreening of several deafness genes depending on patient clinical features.

View Article and Find Full Text PDF

Middle Ear Mechanics in the Barn Owl.

J Morphol

January 2025

Department of Zoology, Denver Museum of Nature & Science, Denver, Colorado, USA.

The barn owl is a common research subject in auditory science due to its exceptional capacity for high frequency hearing and superb sound source localization capabilities. Despite longstanding interest in the auditory performance of barn owls, the function of its middle ear has attracted remarkably little attention. Here, we report the middle ear transfer function measured by laser Doppler vibrometry and direct measurements of inner ear pressures.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!