Cadmium triggers kidney cell apoptosis of purse red common carp (Cyprinus carpio) without caspase-8 activation
- Authors
- Gao, D., Xu, Z., Zhang, X., Zhu, C., Wang, Y., and Min, W.
- ID
- ZDB-PUB-130904-10
- Date
- 2013
- Source
- Developmental and comparative immunology 41(4): 728-737 (Journal)
- Registered Authors
- Keywords
- Caspase-8, apoptosis, cadmium, heavy metal, common carp
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Apoptosis/drug effects*
- Cadmium Compounds/pharmacology*
- Carps/anatomy & histology
- Carps/metabolism
- Carps/physiology*
- Caspase 8/genetics
- Caspase 8/metabolism*
- China
- Cytoplasm/genetics
- Cytoplasm/metabolism
- DNA, Complementary/genetics
- Enzyme Activation
- Epithelial Cells/cytology
- Epithelial Cells/drug effects
- Epithelial Cells/metabolism
- Kidney Tubules/cytology
- Kidney Tubules/drug effects*
- Kidney Tubules/metabolism
- Molecular Sequence Data
- Phylogeny
- Sequence Alignment
- Sequence Homology, Amino Acid
- Sulfates/pharmacology*
- Zebrafish
- PubMed
- 23954723 Full text @ Dev. Comp. Immunol.
Caspase-8, the essential initiator caspase, is believed to play a pivotal role in death receptor-mediated apoptotic pathway. It also participates in mitochondria-mediated apoptosis via cleavage of proapoptotic Bid in mammals. However, its role in fish remains elusive in Cadmium-induced apoptotic pathway. In this study, we isolated the caspase-8 gene from common carp, one of the most important industrial aquatic animals in China using rapid amplification of cDNA ends (RACE). The deduced amino acid sequence of caspase-8 comprised 475 amino acids, which showed approximately 64.1% identity and 79.8% similarity to zebrafish (Danio rerio) caspase-8, possessed two conserved death effector domains, a large subunit and a small subunit. Phylogenetic analysis demonstrated that caspase-8 formed a clade with zebrafish caspase-8. In kidney, cadmium (Cd) exposure triggered apoptosis and increased caspase-3 and -9 activities, whereas it did not affect caspase-8 activity. Real-time quantitative PCR analysis revealed that caspase-8 transcriptional level was not significantly increased in kidney after exposure to Cd. Using Western blot analysis, no caspase-8 cleaved fragment was detected and no significant alteration of procaspase-8 level was found with the same Cd-treated condition. Moreover, the immunopositive staining was predominantly limited to the cytoplasm of renal tubular epithelial cells and no remarkable changes of immunoreactivities were observed using immunohistochemical detection after Cd treatment. The results reveal that Cd can trigger apoptosis, while it cannot activate caspase-8 in purse red common carp.