Related Experiment Video
Updated: Jan 2, 2026

12:17
Initiating Differentiation in Immortalized Multipotent Otic Progenitor Cells
Published on: January 2, 2016
8.9K
Age-related transcriptome changes in Sox2+ supporting cells in the mouse cochlea
Cheng Cheng1,2, Yunfeng Wang3,4, Luo Guo4
1Jiangsu Provincial Key Medical Discipline (Laboratory), Department of Otolaryngology Head and Neck Surgery, Affiliated Drum Tower Hospital of Nanjing University Medical School, No. 321 Zhongshan Road, Nanjing, 210008, China.
Stem Cell Research & Therapy
|December 4, 2019
Summary
Inner ear supporting cells (SCs) lose their hair cell (HC) regeneration ability with age. This study identifies key genes in SCs that change with age, offering potential therapeutic targets for HC regeneration in mammals.
Area of Science:
- Developmental Biology
- Regenerative Medicine
- Otolaryngology
Background:
- Inner ear supporting cells (SCs) in neonatal mice can regenerate hair cells (HCs).
- HC regeneration capacity diminishes significantly in adult mice.
- Understanding age-related changes in SC gene expression is crucial for effective HC regeneration strategies.
Purpose of the Study:
- To investigate age-related changes in the gene expression profiles of mouse cochlear supporting cells (SCs).
- To identify genes influencing the proliferation and HC regeneration potential of SCs across different postnatal ages.
- To discover potential therapeutic targets for enhancing HC regeneration.
Main Methods:
- Isolation of Sox2+ SCs from mouse cochleae at postnatal days 3, 7, 14, and 30 using flow cytometry.
- Transcriptome profiling of isolated SCs via RNA-sequencing (RNA-seq).
- Gene Ontology (GO) analysis to identify age-related and differentially expressed genes.
Main Results:
- Confirmed decreased proliferation and HC regeneration ability of SCs with increasing age.
- Identified numerous age-enriched and differentially expressed genes in SCs, including cell cycle regulators, signaling pathway components, and transcription factors.
- Discovered a set of genes potentially regulating SC proliferation and HC differentiation.
Conclusions:
- Several genes identified may play critical roles in regulating SC proliferation and HC regeneration.
- The generated gene expression datasets offer a valuable resource for developing therapeutic targets for SC-mediated HC regeneration.
- These findings hold promise for future treatments aimed at restoring hearing by regenerating HCs in mammals.
Related Concept Videos
Pleiotropy
43.1K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
43.1K
The Cochlea
50.1K
The cochlea is a coiled structure in the inner ear that contains hair cells—the sensory receptors of the auditory system. Sound waves are transmitted to the cochlea by small bones attached to the eardrum called the ossicles, which vibrate the oval window that leads to the inner ear. This causes fluid in the chambers of the cochlea to move, vibrating the basilar membrane.
50.1K
Hair Cells
44.1K
Hair cells are the sensory receptors of the auditory system—they transduce mechanical sound waves into electrical energy that the nervous system can understand. Hair cells are located in the organ of Corti within the cochlea of the inner ear, between the basilar and tectorial membranes. The actual sensory receptors are called inner hair cells. The outer hair cells serve other functions, such as sound amplification in the cochlea, and are not discussed in detail here.
44.1K

