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Updated: Feb 15, 2026

An Intestine/Liver Microphysiological System for Drug Pharmacokinetic and Toxicological Assessment
Published on: December 3, 2020
Proteomic evidences for microcystin-RR-induced toxicological alterations in mice liver
Ashutosh Kumar Rai1,2,3, Rupesh Chaturvedi4, Ashok Kumar5
1School of Biotechnology, Institute of Science, Banaras Hindu University, Varanasi, 221005, India. akraibiotech@gmail.com.
Abstract:
This study deals with the isolation and purification of an important variant of microcystins namely microcystin-RR (MCYST-RR) from Microcystis aeruginosa and reports its effects on mice liver protein profile and cellular functions. Protein profiling by 2-dimensional gel electrophoresis revealed changes in the number and accumulation of protein spots in liver of mice treated with different concentrations of MCYST-RR. Untreated (control) mice liver showed 368 protein spots while the number was 355, 348 and 332 in liver of mice treated with 200, 300 and 400 µg kg body wt-1 of MCYST-RR respectively. Altogether 102, 97, and 92 spots were differentially up-accumulated and 93, 91, and 87 spots were down- accumulated respectively with the treatment of 200, 300, 400 µg kg body wt-1. Eighteen differentially accumulated proteins present in all the four conditions were identified by MALDI-TOF MS. Of these eighteen proteins, 12 appeared to be involved in apoptosis/toxicological manifestations. Pathway analysis by Reactome and PANTHER database also mapped the identified proteins to programmed cell death/apoptosis clade. That MCYST-RR induces apoptosis in liver tissues was also confirmed by DNA fragmentation assay. Results of this study elucidate the proteomic basis for the hepatotoxicity of MCYST-RR which is otherwise poorly understood till date.
Insights
This study isolated microcystin-RR (MCYST-RR) from Microcystis aeruginosa and found it induces apoptosis in mouse liver. Proteomic analysis revealed significant changes in liver protein profiles, confirming MCYST-RR
Area of Science:
- Environmental toxicology
- Proteomics
- Hepatotoxicity
Background:
- Microcystins are potent toxins produced by cyanobacteria.
- Microcystin-RR (MCYST-RR) is a significant variant with poorly understood toxicological mechanisms.
- Understanding MCYST-RR's effects on liver function is crucial for risk assessment.
Purpose of the Study:
- To isolate and purify MCYST-RR from Microcystis aeruginosa.
- To investigate the effects of MCYST-RR on mouse liver protein profiles and cellular functions.
- To elucidate the proteomic basis of MCYST-RR-induced hepatotoxicity.
Main Methods:
- Isolation and purification of MCYST-RR.
- Two-dimensional gel electrophoresis for protein profiling.
- MALDI-TOF MS for protein identification.
- DNA fragmentation assay for apoptosis confirmation.
Main Results:
- MCYST-RR treatment altered the number and accumulation of protein spots in mouse liver.
- Significant numbers of proteins were differentially up- and down-accumulated in a dose-dependent manner.
- Identified proteins were primarily involved in apoptosis pathways, confirmed by DNA fragmentation assays.
Conclusions:
- MCYST-RR induces apoptosis in liver tissues.
- Proteomic analysis provides insights into the molecular mechanisms of MCYST-RR hepatotoxicity.
- This study enhances the understanding of MCYST-RR's toxicological effects.
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