The small heat shock protein alphaB-crystallin inhibits differentiation-induced caspase 3 activation and myogenic
Ryuji Ikeda1, Kenichi Yoshida, Mina Ushiyama
1Department of Clinical Pharmacy and Pharmacology, Graduate School of Medical and Dental Sciences, Kagoshima University, Sakuragaoka, Kagoshima, Japan. ikeda@m.kufm.kagoshima-u.ac.jp
Abstract:
Myoblasts respond to growth factor deprivation either by diffentiation into multinucleated myotubes or by undergoing apoptosis. The induction of apoptosis and differentiation in myogenic lineage may use overlapping cellular mechanisms. Here we demonstrate that the expression of the small heat shock protein alphaB-crystallin as well as MyoD and myogenin is induced during myogenic differentiation in C2C12 cells, and these inductions occur at an early stage in the differentiation in vitro. To investigate the effect of alphaB-crystallin on myogenic differentiation and apoptosis, C2C12 cells were infected with adenovirus vector bearing full-length alphaB-crystallin cDNA. Overexpression of alphaB-crystallin in C2C12 cells suppressed differentiation-induced apoptosis and activation of caspase 3, and also decreased the expression of MyoD and myogenin during myogenic differentiation of C2C12 cells induced by the differentiation medium. Our findings suggest that stress such as growth factor deprivation plays an important role in triggering apoptosis associated with myogenic differentiation and alphaB-crystallin suppressed the differentiation, apoptosis and caspase 3 activity.
Insights
Small heat shock protein alphaB-crystallin suppresses apoptosis and differentiation in C2C12 myoblasts. Overexpression of alphaB-crystallin reduces MyoD and myogenin, impacting myogenic differentiation and cell death pathways.
Area of Science:
- Cell Biology
- Molecular Biology
- Muscle Development
Background:
- Myoblasts differentiate into myotubes or undergo apoptosis upon growth factor deprivation.
- Apoptosis and differentiation in myogenic lineages may share common cellular pathways.
- Small heat shock proteins, like alphaB-crystallin, are involved in cellular stress responses.
Purpose of the Study:
- To investigate the role of alphaB-crystallin in C2C12 myoblast differentiation and apoptosis.
- To determine the effect of alphaB-crystallin overexpression on myogenic regulatory factors (MyoD, myogenin) and caspase 3 activity.
Main Methods:
- C2C12 myoblasts were cultured and induced to differentiate.
- Adenovirus vectors expressing alphaB-crystallin were used to overexpress the protein.
- Expression levels of alphaB-crystallin, MyoD, and myogenin were analyzed.
- Caspase 3 activity was measured to assess apoptosis.
Main Results:
- AlphaB-crystallin, MyoD, and myogenin expression increased early during C2C12 myogenic differentiation.
- Overexpression of alphaB-crystallin suppressed differentiation-induced apoptosis.
- AlphaB-crystallin overexpression inhibited caspase 3 activation.
- Suppression of differentiation and decreased MyoD/myogenin expression were observed with alphaB-crystallin overexpression.
Conclusions:
- Stress, such as growth factor deprivation, is critical for apoptosis during myogenic differentiation.
- AlphaB-crystallin acts as a suppressor of myogenic differentiation, apoptosis, and caspase 3 activity in C2C12 cells.
- AlphaB-crystallin may modulate overlapping mechanisms involved in differentiation and apoptosis in the myogenic lineage.
Related Concept Videos
Caspases
Master Transcription Regulators
TGF - β Signaling Pathway
The JAK-STAT Signaling Pathway
Hedgehog Signaling Pathway
Bacterial Protein Maturation


