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Published on: April 1, 2011
[Cadmium induces apoptosis of mouse spermatocytes (GC-2 spd) by promoting mitochondrial fission]
1Department of Environmental Health and Occupational Medicine, School of Public Health, Wuhan University of Science and Technology, Wuhan 430065, China.
Abstract:
Objective: To study the underlying mechanism of cadmium-induced apoptosis of mouse spermatocytes (GC-2 spd) . Methods: In March 2021, GC-2 spd cells were exposed to different concentrations of CdCl(2) for 24 hours, namely 5 μmol/L CdCl(2) (low-dose) group and 10 μmol/L CdCl(2) (high-dose) group, and unexposed GC-2 spd cells were used as control group. Mitochondrial morphology was observed in the cells stained with Mito-Track Red CMXRos fluorescent probes by confocal microscopy and the mitochrondrial membrane potential was measured by flow cytometry with JC-1 fluorescent probes. Mitochrondrial proteins, cytosolic proteins and total cellular proteins of GC-2 spd cells were extracted using cell mitochondria isolation kit and RIPA buffer, respectively. The expression of mitochondrial homeostasis regulatory proteins (FIS1 and OPA1), and apoptosis-related proteins (Cytochrome c and cleaved Caspase-3) were examined by Western blot. Results: Compared with the cells in the control group, the relative ratio of JC-1 red/green fluorescence signal in the cells of the low-dose and high-dose CdCl(2) groups decreased significantly (0.740±0.071, 0.570±0.028), with a statistically significant difference (P=0.017, 0.004) ; The morphology of mitochondria changed from long tube to point, and the proportion of cells containing point mitochondria increased significantly (45.1%±3.7% and 25.7%±4.9%), the difference was statistically significant (P=0.005, 0.001) ; The relative expression level of mitochondrial FIS1 in cells of low and high dose CdCl(2) groups was significantly higher (1.271±0.120, 1.693±0.155), the difference was statistically significant (P=0.046, 0.000) ; The relative expression level of OPA1 decreased significantly (0.838±0.050, 0.682±0.040), and the difference was statistically significant (P=0.049, 0.001). Compared with the control group, the relative expression level of cytochrome c protein in the cytoplasm of cells in the low dose group of CdCl(2) was not significantly increased (1.249±0.151), and the difference was not statistically significant (P=0.075). However, the relative expression level in the cytoplasm of cells in the high dose group of CdCl(2) was significantly increased (2.355±0.110), and the difference was statistically significant (P=0.000) ; The relative expression level of Cytochrome c in mitochondria of low and high dose CdCl(2) groups decreased significantly (0.681±0.043, 0.619±0.114), with a statistically significant difference (P=0.004, 0.001) ; Moreover, the level of cleaved Caspase-3 protein in cells gradually increased (5.486±0.544, 11.493±1.739), the difference was statistically significant (P=0.004, 0.000) . Conclusion: Cadmium induced cleaved Caspase-3 mediated apoptosis of GC-2 spd cells via promoting mitochrondrial fission and the release of Cytochrome c from the mitochrondria to the cytosol.
Insights
Cadmium exposure triggers apoptosis in mouse spermatocytes by disrupting mitochondrial function. This process involves increased mitochondrial fission, decreased membrane potential, and release of cytochrome c, ultimately activating cleaved caspase-3.
Area of Science:
- Cell Biology
- Toxicology
- Biochemistry
Context:
- Cadmium is a toxic heavy metal with known adverse effects on reproductive health.
- Spermatocyte apoptosis can lead to male infertility.
- Understanding the molecular mechanisms of cadmium toxicity is crucial for developing protective strategies.
Purpose:
- To elucidate the underlying mechanisms of cadmium-induced apoptosis in mouse spermatocytes (GC-2 spd cells).
- To investigate the role of mitochondrial dysfunction in cadmium-induced cell death.
- To examine the expression of key proteins involved in mitochondrial homeostasis and apoptosis.
Summary:
- Exposure of GC-2 spd cells to cadmium chloride (CdCl2) resulted in significant changes in mitochondrial morphology and a decrease in mitochondrial membrane potential.
- Cadmium exposure altered the expression of mitochondrial proteins FIS1 and OPA1, promoting mitochondrial fission.
- Increased release of cytochrome c from mitochondria to the cytosol and elevated levels of cleaved caspase-3 were observed, indicating apoptosis activation.
Impact:
- This study reveals that cadmium induces apoptosis in spermatocytes through a pathway involving mitochondrial fission and cytochrome c release.
- The findings highlight the critical role of mitochondrial integrity in protecting against cadmium-induced reproductive toxicity.
- Provides insights into the molecular targets for mitigating cadmium's detrimental effects on male fertility.
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