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A Quantitative Detection Method for MicroRNAs in the Kidney of an Ischemic Kidney Injury Mouse Model
Published on: September 11, 2020
MicroRNA profiling in kidney in pigs fed ochratoxin A contaminated diet
Daniela Eliza Marin1, Cornelia Braicu2, Gabi Dumitrescu3
1Laboratory of Animal Biology, National Institute for Research and Development for Biology and Animal Nutrition, Calea Bucuresti No. 1, Balotesti, Ilfov, 077015, Romania.
Abstract:
OTA is a toxic metabolite produced by fungus belonging to Aspergillus and Penicillium genera. Kidney is the main target of this toxin; OTA is considered as one of the etiological factors at the origin of the human Balkan endemic nephropathy. microRNA are short non-coding transcrips (18-22 nucleotides in length) regulating key cellular processes. Various miRNAs have been established to play important roles in development of renal carcinoma and urothelial cancer. The objective of this study is to analyse the miRNA profiling in the kidney of piglets experimentally intoxicated with feed contaminated with OTA. Fifteen piglets (five pigs/group) were randomly distributed into 3 groups, fed normal diet (Group 1: control), or diets contaminated with OTA in two concentrations: 50 μg OTA/kg feed (Group 2: 50 μg OTA/kg feed) or 200 μg OTA/kg feed (Group 3: 200 μg OTA/kg feed) for 28 days. At the end of the experiment blood samples were taken for serological analyses. Animals from control group and 200 μg OTA/kg feed were sacrificed and kidney samples were taken for histological and molecular analyses. As resulted from molecular profiling study there are 8 miRNA differentially expressed in OTA kidney vs control kidney, in which five miRNA were overexpressed in the kidney of OTA intoxicated animals: miR-497 (FC = 6.34), miR-133a-3p (FC = 5.75), miR-423-3p (FC = 5.48), miR-34a (FC = 1.68), miR-542-3p (1.65) while three miRNA were downregulated: miR-421-3p (FC = -3.96); miR-490 (FC = -3.87); miR-9840-3p (FC = -2.13). The altered miRNAs as effect of OTA are strongly connected to the engine of cancer, disturbing nodal points in different pathways, as TP53 signalling. This proof-of-concept study proves the actual utility of miRNAs as biomarkers of mycotoxin exposure, including OTA.
Insights
Ochratoxin A (OTA) exposure alters kidney microRNA profiles in piglets, potentially indicating early signs of kidney damage and cancer risk. These microRNAs may serve as biomarkers for mycotoxin exposure.
Area of Science:
- Toxicology
- Molecular Biology
- Biochemistry
Background:
- Ochratoxin A (OTA) is a nephrotoxic metabolite produced by Aspergillus and Penicillium fungi.
- OTA is implicated in Balkan endemic nephropathy and kidney disease.
- MicroRNAs (miRNAs) are key regulators of cellular processes and are involved in renal cancer development.
Purpose of the Study:
- To investigate the impact of OTA exposure on miRNA expression profiles in piglet kidneys.
- To identify potential miRNA biomarkers for OTA-induced kidney toxicity.
Main Methods:
- Piglets were fed diets with varying concentrations of OTA (0, 50, and 200 μg/kg) for 28 days.
- Kidney tissues were analyzed using molecular profiling to assess miRNA expression.
- Histological and serological analyses were also performed.
Main Results:
- Eight differentially expressed miRNAs were identified in OTA-exposed kidneys compared to controls.
- Five miRNAs (miR-497, miR-133a-3p, miR-423-3p, miR-34a, miR-542-3p) were significantly upregulated.
- Three miRNAs (miR-421-3p, miR-490, miR-9840-3p) were significantly downregulated.
- Altered miRNAs are linked to cancer pathways, including TP53 signaling.
Conclusions:
- OTA exposure significantly alters kidney miRNA expression in piglets.
- These altered miRNAs show potential as biomarkers for mycotoxin exposure and kidney damage.
- Further research can explore the role of these miRNAs in OTA-induced nephrotoxicity and carcinogenesis.
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