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[Apoptosis and apoptosis-related genes in experimental autoimmune inner ear disease]
Liang Chai1, Yang Gao, Zhi-yan Gu
1Department of Otorhinolaryngology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China.
Objective:
To investigate the protein and mRNA expression patterns of apoptosis-related genes, together with evidence of apoptosis, in relation to experimental autoimmune inner ear disease (AIED).
Methods:
Male C57BL/6 mice at 4 weeks age (n = 80) were randomly assigned to one of the five group (n = 16). The inbred mice were given a single subcutaneous injection of diluted solution of pertussis and an emulsion containing equal parts of complete Freund adjuvant (CFA) and inner ear antigens (IEAg) extracted form guinea pig. The animals were sacrificed for inner ear examination at a defined time after the immunization (7, 14, 21 or 28 days). An autoimmune inner ear diseases model was established. Apoptosis was detected by terminal deoxynucleotidyl transferase (TdT)-mediated deoxyuridine triphosphate (d-UTP) nick end-laying (TUNEL) method. Using immunohistochemical techniques and reverse transcriptase polymerase chain reaction to clarify the profile of Fas, FasL, and bcl-2.
Results:
Under normal conditions, no TUNEL-positive cell was observed in the cochlea except for a few positive cells in the supporting cells of Corti's organ and macula sacculi. Inner ear antigens administration induced TUNEL-positive reactions in a wide variety of cells such as inner hair cells, supporting cells, stria vascularis and spiral ligament fibrocytes. No positive staining was evident in outer hair cells, spiral ganglion cells and Scarpa's ganglion cells during the whole period. Fas proteins were expressed in a wide range of cells in inner ear. The levels of Fas mRNA were no significant differences between normal and AIED mice. FasL and bcl-2 proteins could be detected in spiral ganglion cells and Scarpa's ganglion cells both in normal and AIED mice. FasL positive cells increased in number in inner ear of AIED mice. bcl-2 positive cells were not detectable in inner hair cells, stria vascularis and spiral ligament both in normal and AIED mice. The mRNA of three kinds of apoptosis-related genes was detectable in the normal and AIED mice. FasL mRNA was expressed at low levels in normal, being maximal at 14 d post inoculation and decreased gradually to steady levels by 2 weeks. The levels of bcl-2 mRNA increased significantly during the period of AIED.
Conclusion:
Apoptosis mediated by Fas/FasL signal system may play a role in the initiation and maintenance of AIED. bcl-2 has a crucial role in the regulation of the process of apoptosis in the inner ear of AIED mice.
Insights
Apoptosis, detected by TUNEL, increased in experimental autoimmune inner ear disease (AIED) mice. The Fas/FasL system and bcl-2 gene are crucial in AIED pathogenesis and apoptosis regulation.
Area of Science:
- Immunology
- Otolaryngology
- Cell Biology
Background:
- Experimental autoimmune inner ear disease (AIED) is an animal model used to study inner ear inflammation and damage.
- Apoptosis, or programmed cell death, is a critical cellular process implicated in various diseases, including inner ear disorders.
Purpose of the Study:
- To investigate the expression of apoptosis-related genes (Fas, FasL, bcl-2) and the presence of apoptosis in the inner ear of AIED mice.
- To elucidate the role of these genes and apoptosis in the development and progression of AIED.
Main Methods:
- An AIED model was established in C57BL/6 mice using inner ear antigens and complete Freund adjuvant.
- Apoptosis was detected using the TUNEL assay.
- Protein and mRNA expression of Fas, FasL, and bcl-2 were analyzed via immunohistochemistry and RT-PCR.
Main Results:
- TUNEL-positive cells, indicating apoptosis, were significantly increased in various inner ear cells of AIED mice.
- Fas protein was widely expressed, while FasL and bcl-2 proteins were detected in specific cell types.
- FasL mRNA levels peaked at 14 days post-immunization, and bcl-2 mRNA levels increased significantly during AIED.
Conclusions:
- The Fas/FasL signaling pathway appears to be involved in the initiation and maintenance of AIED.
- The bcl-2 gene plays a critical role in regulating apoptosis within the inner ear during AIED.
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