[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.

Abstract

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.

Related Concept Videos

Cellular Injury V: Apoptosis and Autophagy01:22

Cellular Injury V: Apoptosis and Autophagy

Cells respond to damage and stress through highly coordinated processes that decide whether they survive or undergo controlled self-destruction. Two major pathways involved in this regulation are apoptosis, a type of programmed cell death, and autophagy, a survival mechanism that helps cells adapt to adverse conditions.ApoptosisApoptosis removes aged or injured cells to maintain tissue balance. During this process, the cell shrinks, chromatin condenses and fragments, and membrane-bound...
Apoptosis01:30

Apoptosis

Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size reduction of the tissue.
The Intrinsic Apoptotic Pathway01:31

The Intrinsic Apoptotic Pathway

Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
The Extrinsic Apoptotic Pathway01:17

The Extrinsic Apoptotic Pathway

The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
Caspases01:24

Caspases

Caspase, a family of cysteine proteases, serve as effectors in apoptosis. The ced3 gene in C.elegans was first identified to be involved in apoptosis. This gene encodes the ced-3 caspase that is similar to the interleukin-1-beta converting enzyme or ICE in mammals. In addition to apoptosis, caspases also function in the inflammatory response. Inflammatory caspases are essential in activating pro-inflammatory cytokines that recruit immune cells and block the replication of pathogens inside cells.