Related Experiment Video
Updated: Jul 8, 2026

Detection of Mitochondria Membrane Potential to Study CLIC4 Knockdown-induced HN4 Cell Apoptosis In Vitro
Published on: July 17, 2018
Alteration of proteins expression in apoptotic FL cells induced by MCLR
Ming-Luan Xing1, Xiao-Feng Wang, Li-Hong Xu
1Department of Biochemistry and Genetics, School of Medicine, Zhejiang University, 388 Yu Hang Tang Road, Hangzhou 310058, China.
Abstract:
Microcystins (MCs) are a family of monocyclic heptapeptide hepatotoxins produced by freshwater species of cyanobacteria. Microcystin-LR (MCLR) is the most frequently studied and most toxic in over 80 MC congeners. Great deals of studies have demonstrated that MCLR can induce apoptosis in a wide variety of cell types. Although much evidence indicates that mitochondria play a pivotal role in MCLR-induced apoptosis, the complicated apoptosis mechanisms induced by MCLR have not been completely characterized. It is possible that there are other apoptotic pathways existing in MCLR-induced apoptosis. The present study was undertaken to determine the expression of PP2A, CHOP, Bax, Bcl-2, and p53 proteins in MCLR-induced apoptosis in FL cells. The results showed that MCLR could induce apoptosis in FL cells and the process was accompanied with the upregulation of PP2A, Bax, and p53 proteins and the downregulation of Bcl-2 proteins. In addition, the CHOP protein was upregulated at most treatment groups and decreased at the highest concentration group. These results, especially the alteration of PP2A and CHOP proteins might provide new insights into MCLR-induced apoptosis.
Insights
Microcystin-LR (MCLR) triggers apoptosis in FL cells by altering key protein levels. This study reveals new insights into the complex mechanisms of microcystin-induced cell death, focusing on PP2A and CHOP proteins.
Area of Science:
- Toxicology
- Cell Biology
- Biochemistry
Background:
- Microcystins (MCs) are cyanobacterial hepatotoxins, with Microcystin-LR (MCLR) being the most potent and studied congener.
- MCLR is known to induce apoptosis across various cell types, with mitochondria playing a significant role.
- The precise molecular mechanisms and all apoptotic pathways involved in MCLR-induced cell death remain incompletely understood.
Purpose of the Study:
- To investigate the expression of specific proteins involved in apoptosis following MCLR exposure in FL cells.
- To elucidate the roles of Protein Phosphatase 2A (PP2A), C/EBP homologous protein (CHOP), Bax, Bcl-2, and p53 in MCLR-induced apoptosis.
- To gain new insights into the complex apoptotic pathways activated by MCLR.
Main Methods:
- FL cells were treated with varying concentrations of MCLR.
- Protein expression levels of PP2A, CHOP, Bax, Bcl-2, and p53 were analyzed using Western blotting or similar techniques.
- Apoptosis induction by MCLR was confirmed in FL cells.
Main Results:
- MCLR treatment induced apoptosis in FL cells.
- Significant upregulation of PP2A, Bax, and p53 proteins was observed.
- Bcl-2 protein levels were downregulated, while CHOP protein showed upregulation in most treatment groups, decreasing at the highest concentration.
- Alterations in PP2A and CHOP protein expression were particularly noted.
Conclusions:
- MCLR induces apoptosis in FL cells through modulation of key apoptotic regulatory proteins.
- The observed changes in PP2A and CHOP protein expression offer novel perspectives on MCLR-induced apoptotic pathways.
- This study contributes to a deeper understanding of the molecular mechanisms underlying microcystin toxicity.
Related Concept Videos
Phagocytosis of Apoptotic Cells
Normal cells contain receptors that prevent them from being recognized by phagocytes.
The Extrinsic Apoptotic Pathway
The Intrinsic Apoptotic Pathway
Regulated Protein Degradation
Protein degradation plays two important roles in the cells. It helps to protect cells from misfolded or damaged proteins before they lead to a...
Apoptosis
Cellular Injury V: Apoptosis and Autophagy

